Role: Associate Scientist Contract: 12-month Location: Speke, Liverpool (on site) Hours: Full-time, Monday to Thursday 8:00am to 4:45pm, Friday 8:00am to 1:00pm Team: Analytical Testing Flu Biopharmaceutical Development About our client Our client's Liverpool site in Speke manufactures a nasal influenza vaccine that helps protect people against seasonal flu. Their teams work to a demanding timeline every year to deliver a vaccine that is safe, effective and ready for the new flu season. The Flu BPD department brings together specialist teams across Analytical Development and Testing, Process Development, Virology Research and Strain Development. Together they characterise candidate vaccine virus strains and generate the high-quality data that supports key commercial decisions. It is a multidisciplinary team of scientists. About the role The data you generate will directly inform commercial decisions for a nasal flu vaccine. This is a chance to see your science make a real impact on patients, from the lab bench to the decisions that shape each flu season. You will join the Analytical Testing team on a 12-month contract, providing the testing that allows candidate vaccine virus strains to be characterised and understood. This is a fast-paced, almost entirely laboratory-based role. Key responsibilities Provide laboratory testing to support the characterisation and understanding of candidate vaccine virus strains Perform a range of analytical methods, including biological cell-based assays Work with automated laboratory equipment to deliver testing efficiently and consistently Use assay controls appropriately to generate robust, high-quality datasets that support commercial decisions Deliver timely, right-first-time data to meet seasonal timelines Work in line with Good Laboratory Practice (GLP) Record work accurately and keep electronic laboratory records up to date Work as an embedded member of the team, flexing to changing priorities and learning new methods as needed What you'll gain Hands-on technical experience: develop your skills in biological cell-based assays and work with advanced laboratory automation Industrial laboratory exposure: gain experience in a fast-paced industrial laboratory, supporting a vaccine that protects patients Structured development and training: a structured programme to help you build your capability and grow your career About you Essential A minimum of an undergraduate degree in a Biological Sciences discipline A passion for analytical techniques and for generating excellent data that supports commercial decisions A good working knowledge of GLP An understanding of how assay controls are used to produce robust datasets Excellent attention to detail, including keeping electronic laboratory records accurate and up to date Excellent teamwork skills and the ability to work as an embedded member of a team Flexibility and a willingness to learn new methods The ability to think on your feet and solve problems Learning agility: you learn quickly and can hit the ground running A passion for working in industry in a fast-paced environment Desirable A Master's degree in a Biological Sciences discipline A passion for virology Experience of working with biological assays Previous experience in an industrial laboratory setting What will set you apart You are passionate about science and want to make a difference to patients. You are curious and eager to learn, you take ownership of your personal development, and you bring the energy to thrive in a fast-paced, team-focused laboratory environment. Please note: this is a full-time, on-site, laboratory-based role. Guidant, Carbon60, Lorien & SRG - The Vertage Group Portfolio are acting as an Employment Business in relation to this vacancy.
Nov 12, 2026
Seasonal
Role: Associate Scientist Contract: 12-month Location: Speke, Liverpool (on site) Hours: Full-time, Monday to Thursday 8:00am to 4:45pm, Friday 8:00am to 1:00pm Team: Analytical Testing Flu Biopharmaceutical Development About our client Our client's Liverpool site in Speke manufactures a nasal influenza vaccine that helps protect people against seasonal flu. Their teams work to a demanding timeline every year to deliver a vaccine that is safe, effective and ready for the new flu season. The Flu BPD department brings together specialist teams across Analytical Development and Testing, Process Development, Virology Research and Strain Development. Together they characterise candidate vaccine virus strains and generate the high-quality data that supports key commercial decisions. It is a multidisciplinary team of scientists. About the role The data you generate will directly inform commercial decisions for a nasal flu vaccine. This is a chance to see your science make a real impact on patients, from the lab bench to the decisions that shape each flu season. You will join the Analytical Testing team on a 12-month contract, providing the testing that allows candidate vaccine virus strains to be characterised and understood. This is a fast-paced, almost entirely laboratory-based role. Key responsibilities Provide laboratory testing to support the characterisation and understanding of candidate vaccine virus strains Perform a range of analytical methods, including biological cell-based assays Work with automated laboratory equipment to deliver testing efficiently and consistently Use assay controls appropriately to generate robust, high-quality datasets that support commercial decisions Deliver timely, right-first-time data to meet seasonal timelines Work in line with Good Laboratory Practice (GLP) Record work accurately and keep electronic laboratory records up to date Work as an embedded member of the team, flexing to changing priorities and learning new methods as needed What you'll gain Hands-on technical experience: develop your skills in biological cell-based assays and work with advanced laboratory automation Industrial laboratory exposure: gain experience in a fast-paced industrial laboratory, supporting a vaccine that protects patients Structured development and training: a structured programme to help you build your capability and grow your career About you Essential A minimum of an undergraduate degree in a Biological Sciences discipline A passion for analytical techniques and for generating excellent data that supports commercial decisions A good working knowledge of GLP An understanding of how assay controls are used to produce robust datasets Excellent attention to detail, including keeping electronic laboratory records accurate and up to date Excellent teamwork skills and the ability to work as an embedded member of a team Flexibility and a willingness to learn new methods The ability to think on your feet and solve problems Learning agility: you learn quickly and can hit the ground running A passion for working in industry in a fast-paced environment Desirable A Master's degree in a Biological Sciences discipline A passion for virology Experience of working with biological assays Previous experience in an industrial laboratory setting What will set you apart You are passionate about science and want to make a difference to patients. You are curious and eager to learn, you take ownership of your personal development, and you bring the energy to thrive in a fast-paced, team-focused laboratory environment. Please note: this is a full-time, on-site, laboratory-based role. Guidant, Carbon60, Lorien & SRG - The Vertage Group Portfolio are acting as an Employment Business in relation to this vacancy.
Summary: Do you have knowledge of water process science? Can you interpret data and turn it into easy-to-understand information? Are you looking for a role that has variety? If the answer is yes, this is a chance to take the next step in your career We want to be the water company people want to be supplied by and want to work for. In this role as a Process Scientist in our Water Quality department, you will be instrumental in the safe and efficient management of our water treatment works. A key aspect of the position is close collaboration with Distribution Technicians, providing them with expert guidance on water treatment procedures. Additionally, you will be responsible for detailed monitoring of data trends and the systematic investigation of anomalies. Your ability to apply a logical, methodical approach will enable you to effectively investigate water quality concerns and advise on the most appropriate corrective actions. Every day is different in this role - you'll be carrying out a mix of data analysis and on-site investigation of water quality failures at our Kent water treatment sites. Your scientific background and water treatment experience will enable you to effectively troubleshoot and determine the root cause of these issues. You will also be responsible for technical report writing, including recommendations for compliance and investigation documentation; therefore, experience in technical report writing is preferred. You're self-motivated, well organised and enjoy problem solving. We're a friendly, open and collaborative team that will give you lots of encouragement to share your ideas and make a difference to the success of our growing Process Science team. This role is based at our Farnborough office, with site visits around the Hampshire area and some home working. Standard working hours are 08:30 - 17:00 - you will also be put on a standby rota to cover out of hours support. Main responsibilities: Optimise the performance and maximise the efficiency of water treatment processes. Investigate the cause of compliance/operational water quality breaches. Provide a comprehensive report detailing the findings and conclusions of the investigation. Undertake water treatment works site process audits in a timely manner. Prepare technical reports with conclusions & recommendations as required. Provision of technical support and advice to the business. To provide standby Water Quality cover out of hours for the business. You'll need: Skills / Qualifications / Experience Qualified with a science degree or have relevant experience in process water treatment background Self-motivated, committed and organised with a knowledge of water treatment processes Hold a valid driving licence Employees are required to be flexible and to be prepared to perform duties and other tasks within their capabilities. The nature of our business is such that the contents of any job profile are subject to change from time to time. Grow a career with a meaningful purpose. We know the communities we serve are diverse. We recognise creativity comes from diversity not similarity. That's why we are enthusiastic about creating inclusion across age, race, gender, ethnicity, religion and identity. You will experience our dedication to equal opportunities and fair treatment for all: through your recruitment, employment and career progression with South East Water. Benefits package: Excellent Stakeholder pension scheme, up to 10% employer contribution. 5 weeks holiday plus bank holidays per annum, increasing to 6 weeks with length of service. Flexible annual leave policy to buy or sell holiday leave. Paid volunteering days. Cycle to work scheme. Health cash plan. Life assurance. Wellbeing related benefits. What can you expect from your recruitment? To apply for this position, please submit your CV on our career's website. It is necessary for you to have the legal right to work in the UK when you begin employment with South East Water. Additionally, as part of the employment offer, you will need to pass background, identity, and employment referencing checks. If this sounds like the opportunity you've been looking for, apply now! South East Water kindly asks that recruitment agencies refrain from submitting CVs to our employees or associates without explicit invitation from our HR Resourcing team. CVs sent on a speculative basis will not be acknowledged and will not assume any responsibility for fees or commissions in the event that we hire a candidate who applied directly or subsequently introduced by an instructed agency. Compensation package: £31,733 - £41,930 depending on experience
Nov 12, 2026
Full time
Summary: Do you have knowledge of water process science? Can you interpret data and turn it into easy-to-understand information? Are you looking for a role that has variety? If the answer is yes, this is a chance to take the next step in your career We want to be the water company people want to be supplied by and want to work for. In this role as a Process Scientist in our Water Quality department, you will be instrumental in the safe and efficient management of our water treatment works. A key aspect of the position is close collaboration with Distribution Technicians, providing them with expert guidance on water treatment procedures. Additionally, you will be responsible for detailed monitoring of data trends and the systematic investigation of anomalies. Your ability to apply a logical, methodical approach will enable you to effectively investigate water quality concerns and advise on the most appropriate corrective actions. Every day is different in this role - you'll be carrying out a mix of data analysis and on-site investigation of water quality failures at our Kent water treatment sites. Your scientific background and water treatment experience will enable you to effectively troubleshoot and determine the root cause of these issues. You will also be responsible for technical report writing, including recommendations for compliance and investigation documentation; therefore, experience in technical report writing is preferred. You're self-motivated, well organised and enjoy problem solving. We're a friendly, open and collaborative team that will give you lots of encouragement to share your ideas and make a difference to the success of our growing Process Science team. This role is based at our Farnborough office, with site visits around the Hampshire area and some home working. Standard working hours are 08:30 - 17:00 - you will also be put on a standby rota to cover out of hours support. Main responsibilities: Optimise the performance and maximise the efficiency of water treatment processes. Investigate the cause of compliance/operational water quality breaches. Provide a comprehensive report detailing the findings and conclusions of the investigation. Undertake water treatment works site process audits in a timely manner. Prepare technical reports with conclusions & recommendations as required. Provision of technical support and advice to the business. To provide standby Water Quality cover out of hours for the business. You'll need: Skills / Qualifications / Experience Qualified with a science degree or have relevant experience in process water treatment background Self-motivated, committed and organised with a knowledge of water treatment processes Hold a valid driving licence Employees are required to be flexible and to be prepared to perform duties and other tasks within their capabilities. The nature of our business is such that the contents of any job profile are subject to change from time to time. Grow a career with a meaningful purpose. We know the communities we serve are diverse. We recognise creativity comes from diversity not similarity. That's why we are enthusiastic about creating inclusion across age, race, gender, ethnicity, religion and identity. You will experience our dedication to equal opportunities and fair treatment for all: through your recruitment, employment and career progression with South East Water. Benefits package: Excellent Stakeholder pension scheme, up to 10% employer contribution. 5 weeks holiday plus bank holidays per annum, increasing to 6 weeks with length of service. Flexible annual leave policy to buy or sell holiday leave. Paid volunteering days. Cycle to work scheme. Health cash plan. Life assurance. Wellbeing related benefits. What can you expect from your recruitment? To apply for this position, please submit your CV on our career's website. It is necessary for you to have the legal right to work in the UK when you begin employment with South East Water. Additionally, as part of the employment offer, you will need to pass background, identity, and employment referencing checks. If this sounds like the opportunity you've been looking for, apply now! South East Water kindly asks that recruitment agencies refrain from submitting CVs to our employees or associates without explicit invitation from our HR Resourcing team. CVs sent on a speculative basis will not be acknowledged and will not assume any responsibility for fees or commissions in the event that we hire a candidate who applied directly or subsequently introduced by an instructed agency. Compensation package: £31,733 - £41,930 depending on experience
Summary: Do you have knowledge of water process science? Can you interpret data and turn it into easy-to-understand information? Are you looking for a role that has variety? If the answer is yes, this is a chance to take the next step in your career We want to be the water company people want to be supplied by and want to work for. In this role as a Process Scientist in our Water Quality department, you will be instrumental in the safe and efficient management of our water treatment works. A key aspect of the position is close collaboration with Distribution Technicians, providing them with expert guidance on water treatment procedures. Additionally, you will be responsible for detailed monitoring of data trends and the systematic investigation of anomalies. Your ability to apply a logical, methodical approach will enable you to effectively investigate water quality concerns and advise on the most appropriate corrective actions. Every day is different in this role - you'll be carrying out a mix of data analysis and on-site investigation of water quality failures at our Kent water treatment sites. Your scientific background and water treatment experience will enable you to effectively troubleshoot and determine the root cause of these issues. You will also be responsible for technical report writing, including recommendations for compliance and investigation documentation; therefore, experience in technical report writing is preferred. You're self-motivated, well organised and enjoy problem solving. We're a friendly, open and collaborative team that will give you lots of encouragement to share your ideas and make a difference to the success of our growing Process Science team. This role is based at our Pembury office, with site visits around the Kent area and some home working. Standard working hours are 08:30 - 17:00 - you will also be put on a standby rota to cover out of hours support. Main responsibilities: Optimise the performance and maximise the efficiency of water treatment processes. Investigate the cause of compliance/operational water quality breaches. Provide a comprehensive report detailing the findings and conclusions of the investigation. Undertake water treatment works site process audits in a timely manner. Prepare technical reports with conclusions & recommendations as required. Provision of technical support and advice to the business. Provide standby Water Quality cover out of hours for the business. You'll need: Skills / Experience / Qualifications A degree in a Scientific subject or experience in a water-based role. Knowledge of water treatment processes. Technical report writing skills. Strong communication skills. A full, clean driving license. Grow a career with a meaningful purpose. We know the communities we serve are diverse. We recognise creativity comes from diversity not similarity. That's why we are enthusiastic about creating inclusion across age, race, gender, ethnicity, religion and identity. You will experience our dedication to equal opportunities and fair treatment for all: through your recruitment, employment and career progression with South East Water. Benefits package: Excellent Stakeholder pension scheme, up to 10% employer contribution. 5 weeks holiday plus bank holidays per annum, increasing to 6 weeks with length of service. Flexible annual leave policy to buy or sell holiday leave. Paid volunteering days. Cycle to work scheme. Health cash plan. Life assurance. Wellbeing related benefits. What can you expect from your recruitment? To apply for this position, please submit your CV on our career's website. It is necessary for you to have the legal right to work in the UK when you begin employment with South East Water. Additionally, as part of the employment offer, you will need to pass background, identity, and employment referencing checks. If this sounds like the opportunity you've been looking for, apply now! South East Water kindly asks that recruitment agencies refrain from submitting CVs to our employees or associates without explicit invitation from our HR Resourcing team. CVs sent on a speculative basis will not be acknowledged and will not assume any responsibility for fees or commissions in the event that we hire a candidate who applied directly or subsequently introduced by an instructed agency. Compensation package: £31,733 - £41,930 depending on experience
Nov 12, 2026
Full time
Summary: Do you have knowledge of water process science? Can you interpret data and turn it into easy-to-understand information? Are you looking for a role that has variety? If the answer is yes, this is a chance to take the next step in your career We want to be the water company people want to be supplied by and want to work for. In this role as a Process Scientist in our Water Quality department, you will be instrumental in the safe and efficient management of our water treatment works. A key aspect of the position is close collaboration with Distribution Technicians, providing them with expert guidance on water treatment procedures. Additionally, you will be responsible for detailed monitoring of data trends and the systematic investigation of anomalies. Your ability to apply a logical, methodical approach will enable you to effectively investigate water quality concerns and advise on the most appropriate corrective actions. Every day is different in this role - you'll be carrying out a mix of data analysis and on-site investigation of water quality failures at our Kent water treatment sites. Your scientific background and water treatment experience will enable you to effectively troubleshoot and determine the root cause of these issues. You will also be responsible for technical report writing, including recommendations for compliance and investigation documentation; therefore, experience in technical report writing is preferred. You're self-motivated, well organised and enjoy problem solving. We're a friendly, open and collaborative team that will give you lots of encouragement to share your ideas and make a difference to the success of our growing Process Science team. This role is based at our Pembury office, with site visits around the Kent area and some home working. Standard working hours are 08:30 - 17:00 - you will also be put on a standby rota to cover out of hours support. Main responsibilities: Optimise the performance and maximise the efficiency of water treatment processes. Investigate the cause of compliance/operational water quality breaches. Provide a comprehensive report detailing the findings and conclusions of the investigation. Undertake water treatment works site process audits in a timely manner. Prepare technical reports with conclusions & recommendations as required. Provision of technical support and advice to the business. Provide standby Water Quality cover out of hours for the business. You'll need: Skills / Experience / Qualifications A degree in a Scientific subject or experience in a water-based role. Knowledge of water treatment processes. Technical report writing skills. Strong communication skills. A full, clean driving license. Grow a career with a meaningful purpose. We know the communities we serve are diverse. We recognise creativity comes from diversity not similarity. That's why we are enthusiastic about creating inclusion across age, race, gender, ethnicity, religion and identity. You will experience our dedication to equal opportunities and fair treatment for all: through your recruitment, employment and career progression with South East Water. Benefits package: Excellent Stakeholder pension scheme, up to 10% employer contribution. 5 weeks holiday plus bank holidays per annum, increasing to 6 weeks with length of service. Flexible annual leave policy to buy or sell holiday leave. Paid volunteering days. Cycle to work scheme. Health cash plan. Life assurance. Wellbeing related benefits. What can you expect from your recruitment? To apply for this position, please submit your CV on our career's website. It is necessary for you to have the legal right to work in the UK when you begin employment with South East Water. Additionally, as part of the employment offer, you will need to pass background, identity, and employment referencing checks. If this sounds like the opportunity you've been looking for, apply now! South East Water kindly asks that recruitment agencies refrain from submitting CVs to our employees or associates without explicit invitation from our HR Resourcing team. CVs sent on a speculative basis will not be acknowledged and will not assume any responsibility for fees or commissions in the event that we hire a candidate who applied directly or subsequently introduced by an instructed agency. Compensation package: £31,733 - £41,930 depending on experience
Machine Learning Python Data Science Industrial Analytics Predictive Modelling Process Optimisation Imagine using advanced analytics to predict problems before they happen, improve manufacturing performance and help industrial plants operate more efficiently. Not through hypothetical datasets, but by working with real industrial processes, real customers and data that makes a measurable difference. Welcome to Keit. We're an innovative UK technology company developing advanced analytical solutions that help manufacturers understand and optimise their processes in real time. Our technology combines spectroscopy, industrial process data and intelligent software to unlock insights that traditional monitoring methods can't provide. Now we're looking for a talented Process Intelligence Scientist to help take that capability to the next level. The Role at a Glance Process Intelligence Scientist Harwell Campus, Didcot, Oxfordshire Office-Based £45,000 £65,000 DOE Full Time Permanent Monday Friday, 9am 5:30pm (Some Flexibility Available) Occasional International Travel, Primarily North America Sector: Industrial Analytics Machine Learning Spectroscopy Process Technology Your Background / Skills: Python, Machine Learning, Data Science, Statistics, Predictive Modelling, Industrial Data, Process Analytics, Time-Series Analysis, Chemometrics, Process Optimisation. Candidates must already have the unrestricted right to work in the UK. The Keit Story At Keit, we're passionate about making complex industrial processes easier to understand, monitor and improve. Our IRmadillo spectrometer platform provides advanced, real-time chemical analysis, while our IRis software platform combines spectroscopy, laboratory measurements and operational data to deliver meaningful process insights. Today, our technology helps customers in the fuel ethanol industry monitor and optimise fermentation. But we're only scratching the surface. With access to an increasingly rich dataset across industrial plants, we see exciting opportunities to use machine learning to predict yield losses, detect anomalies, improve efficiency and identify maintenance needs. And beyond fermentation, there's the potential to expand into entirely new processes and industries. We're not simply collecting data. We're turning it into intelligence that could transform how industrial plants operate. Your Role in the Story As our Process Intelligence Scientist, you'll work at the intersection of machine learning, chemistry, industrial processes and software development. You'll develop predictive models, improve existing chemometric capabilities and explore new ways to turn complex process data into practical recommendations for customers. Working closely with chemometricians, software developers and customer engineering teams, you'll understand real operational challenges and develop solutions that create measurable value. This is a hands-on opportunity to combine technical problem-solving, experimentation and customer collaboration while helping shape the future of our IRis platform. What success looks like: • Develop predictive models using spectroscopy, laboratory measurements and industrial process data. • Apply machine learning and statistics to identify inefficiencies, yield losses, contamination risks and equipment deviations. • Improve chemometric models, including calibration development, validation and ongoing performance. • Explore time-series modelling, anomaly detection and advanced process optimisation techniques. • Help automate model development, maintenance and deployment workflows. • Work directly with customers to understand operational challenges, data quality and sampling requirements. • Collaborate with software developers to turn analytical methods into scalable product capabilities. • Identify opportunities to expand IRis into new process areas and industries. • Use evidence and experimentation to improve performance and shape future analytical capabilities. About You You're a curious data scientist or analytical specialist who enjoys solving difficult problems and finding meaningful insights in complex information. You're comfortable working with incomplete, noisy and imperfect datasets, and enjoy translating technical ideas into practical solutions. You'll also bring: • Strong foundations in machine learning, statistics or data science. • Excellent Python programming skills and hands-on predictive modelling experience. • Proven ability to extract valuable insights from messy, real-world datasets. • Experience developing and applying statistical or machine learning models to practical problems. • Strong analytical reasoning and an evidence-led approach to problem-solving. • The confidence to explain complex technical concepts clearly to non-specialists. • A collaborative, customer-focused mindset and the initiative to turn ideas into working solutions. Highly Desirable • Experience within industrial biotechnology, fermentation, manufacturing or process industries. • Knowledge of chemometrics, including PLS, PCA, spectral preprocessing or calibration development. • Experience with spectroscopy or analytical instrumentation. • Time-series analytics, anomaly detection or industrial process optimisation. • Familiarity with Azure-based data and analytics environments. The Person We're Looking For We value potential and attitude just as highly as existing industry knowledge. You don't need to know everything about spectroscopy or fermentation, but you do need the curiosity and technical foundations to learn quickly. You'll thrive in a team that debates ideas constructively, challenges assumptions and makes evidence-based decisions. At Keit, we believe the best solutions come from collaboration, continuous improvement and being willing to experiment, even when that means occasionally getting things wrong. What's on Offer • £45,000 £65,000 Salary Depending on Experience • Some Flexibility in Working Hours • The Opportunity to Work with Advanced Spectroscopy and Machine Learning Technology • Direct Exposure to Industrial Challenges and International Customers • The Chance to Influence Future Product Capabilities and Technical Direction • Collaboration with Experienced Scientists, Engineers and Software Developers • A Supportive, Collaborative and Evidence-Led Working Environment • A Key Role in Building Keit's Future Process Intelligence Capability Why Join Keit? This is more than another data science role. It's an opportunity to apply your technical expertise to real industrial challenges, where better predictions and smarter decisions can directly improve manufacturing performance. You'll work with a unique combination of spectroscopy, laboratory and operational data, developing solutions that have genuine practical value. And you'll help shape a technology platform with the potential to transform process monitoring and optimisation across multiple industries. Ready to Turn Data into Something Extraordinary? If you're a talented machine learning or data science professional who loves solving complex problems and wants to help build the future of industrial process intelligence, we'd love to hear from you. Apply now and help shape the next chapter of Keit. Application Notice We take your privacy seriously. As you might expect, you may be contacted by email, text or telephone. Your data is processed by our talent partner RR (Recruitment Revolution) on the basis of their legitimate interests in fulfilling the recruitment process. Please refer to their Data Privacy Policy & Notice on their website for further details.
Nov 11, 2026
Full time
Machine Learning Python Data Science Industrial Analytics Predictive Modelling Process Optimisation Imagine using advanced analytics to predict problems before they happen, improve manufacturing performance and help industrial plants operate more efficiently. Not through hypothetical datasets, but by working with real industrial processes, real customers and data that makes a measurable difference. Welcome to Keit. We're an innovative UK technology company developing advanced analytical solutions that help manufacturers understand and optimise their processes in real time. Our technology combines spectroscopy, industrial process data and intelligent software to unlock insights that traditional monitoring methods can't provide. Now we're looking for a talented Process Intelligence Scientist to help take that capability to the next level. The Role at a Glance Process Intelligence Scientist Harwell Campus, Didcot, Oxfordshire Office-Based £45,000 £65,000 DOE Full Time Permanent Monday Friday, 9am 5:30pm (Some Flexibility Available) Occasional International Travel, Primarily North America Sector: Industrial Analytics Machine Learning Spectroscopy Process Technology Your Background / Skills: Python, Machine Learning, Data Science, Statistics, Predictive Modelling, Industrial Data, Process Analytics, Time-Series Analysis, Chemometrics, Process Optimisation. Candidates must already have the unrestricted right to work in the UK. The Keit Story At Keit, we're passionate about making complex industrial processes easier to understand, monitor and improve. Our IRmadillo spectrometer platform provides advanced, real-time chemical analysis, while our IRis software platform combines spectroscopy, laboratory measurements and operational data to deliver meaningful process insights. Today, our technology helps customers in the fuel ethanol industry monitor and optimise fermentation. But we're only scratching the surface. With access to an increasingly rich dataset across industrial plants, we see exciting opportunities to use machine learning to predict yield losses, detect anomalies, improve efficiency and identify maintenance needs. And beyond fermentation, there's the potential to expand into entirely new processes and industries. We're not simply collecting data. We're turning it into intelligence that could transform how industrial plants operate. Your Role in the Story As our Process Intelligence Scientist, you'll work at the intersection of machine learning, chemistry, industrial processes and software development. You'll develop predictive models, improve existing chemometric capabilities and explore new ways to turn complex process data into practical recommendations for customers. Working closely with chemometricians, software developers and customer engineering teams, you'll understand real operational challenges and develop solutions that create measurable value. This is a hands-on opportunity to combine technical problem-solving, experimentation and customer collaboration while helping shape the future of our IRis platform. What success looks like: • Develop predictive models using spectroscopy, laboratory measurements and industrial process data. • Apply machine learning and statistics to identify inefficiencies, yield losses, contamination risks and equipment deviations. • Improve chemometric models, including calibration development, validation and ongoing performance. • Explore time-series modelling, anomaly detection and advanced process optimisation techniques. • Help automate model development, maintenance and deployment workflows. • Work directly with customers to understand operational challenges, data quality and sampling requirements. • Collaborate with software developers to turn analytical methods into scalable product capabilities. • Identify opportunities to expand IRis into new process areas and industries. • Use evidence and experimentation to improve performance and shape future analytical capabilities. About You You're a curious data scientist or analytical specialist who enjoys solving difficult problems and finding meaningful insights in complex information. You're comfortable working with incomplete, noisy and imperfect datasets, and enjoy translating technical ideas into practical solutions. You'll also bring: • Strong foundations in machine learning, statistics or data science. • Excellent Python programming skills and hands-on predictive modelling experience. • Proven ability to extract valuable insights from messy, real-world datasets. • Experience developing and applying statistical or machine learning models to practical problems. • Strong analytical reasoning and an evidence-led approach to problem-solving. • The confidence to explain complex technical concepts clearly to non-specialists. • A collaborative, customer-focused mindset and the initiative to turn ideas into working solutions. Highly Desirable • Experience within industrial biotechnology, fermentation, manufacturing or process industries. • Knowledge of chemometrics, including PLS, PCA, spectral preprocessing or calibration development. • Experience with spectroscopy or analytical instrumentation. • Time-series analytics, anomaly detection or industrial process optimisation. • Familiarity with Azure-based data and analytics environments. The Person We're Looking For We value potential and attitude just as highly as existing industry knowledge. You don't need to know everything about spectroscopy or fermentation, but you do need the curiosity and technical foundations to learn quickly. You'll thrive in a team that debates ideas constructively, challenges assumptions and makes evidence-based decisions. At Keit, we believe the best solutions come from collaboration, continuous improvement and being willing to experiment, even when that means occasionally getting things wrong. What's on Offer • £45,000 £65,000 Salary Depending on Experience • Some Flexibility in Working Hours • The Opportunity to Work with Advanced Spectroscopy and Machine Learning Technology • Direct Exposure to Industrial Challenges and International Customers • The Chance to Influence Future Product Capabilities and Technical Direction • Collaboration with Experienced Scientists, Engineers and Software Developers • A Supportive, Collaborative and Evidence-Led Working Environment • A Key Role in Building Keit's Future Process Intelligence Capability Why Join Keit? This is more than another data science role. It's an opportunity to apply your technical expertise to real industrial challenges, where better predictions and smarter decisions can directly improve manufacturing performance. You'll work with a unique combination of spectroscopy, laboratory and operational data, developing solutions that have genuine practical value. And you'll help shape a technology platform with the potential to transform process monitoring and optimisation across multiple industries. Ready to Turn Data into Something Extraordinary? If you're a talented machine learning or data science professional who loves solving complex problems and wants to help build the future of industrial process intelligence, we'd love to hear from you. Apply now and help shape the next chapter of Keit. Application Notice We take your privacy seriously. As you might expect, you may be contacted by email, text or telephone. Your data is processed by our talent partner RR (Recruitment Revolution) on the basis of their legitimate interests in fulfilling the recruitment process. Please refer to their Data Privacy Policy & Notice on their website for further details.
Regulatory Affairs Manager Medical Devices London Hybrid Permanent I Salary Dependant on Experience I m working exclusively with an innovative, venture-backed medical device company in London that is gearing up for a FDA 510(k) submission. They re hiring a Regulatory Affairs Manager, who will own regulatory strategy from day one. The role Lead the company s 510(k) through FDA review and clearance, including predicate strategy, substantial equivalence and Additional Information responses Act as the primary FDA contact and lead Pre-Submission meetings Coordinate test evidence across engineering, CROs and test houses (electrical safety, software, biocompatibility, bench, sterilisation) Build US post-market processes: registration and listing, UDI/GUDID, MDR, complaints and recalls Assess design and manufacturing changes for 510(k) impact Shape the UK and EU MDR strategy as the business grows Grow the regulatory function over time, including budgets, consultants and, in time, a team What you ll bring 6-7+ years regulatory affairs experience in medical devices Hands-on authorship of at least one successful FDA 510(k) Direct FDA interaction experience, such as Pre-Subs and AI responses Working knowledge of 21 CFR 820 (QMSR), ISO 13485 and ISO 14971 Experience with active or electromechanical Class II/III devices (IEC 60601, IEC 62304) is a strong plus EU MDR and RAC are a bonus Comfortable in a small, fast-moving team where you ll be hands-on Right to work in the UK (sponsorship is not available) Why it s worth a look You ll own regulatory strategy at the most important point in the company s life: FDA submission and US launch A direct line to the CEO, with real influence on the business Equity through share options Occasional US and European travel
Nov 11, 2026
Full time
Regulatory Affairs Manager Medical Devices London Hybrid Permanent I Salary Dependant on Experience I m working exclusively with an innovative, venture-backed medical device company in London that is gearing up for a FDA 510(k) submission. They re hiring a Regulatory Affairs Manager, who will own regulatory strategy from day one. The role Lead the company s 510(k) through FDA review and clearance, including predicate strategy, substantial equivalence and Additional Information responses Act as the primary FDA contact and lead Pre-Submission meetings Coordinate test evidence across engineering, CROs and test houses (electrical safety, software, biocompatibility, bench, sterilisation) Build US post-market processes: registration and listing, UDI/GUDID, MDR, complaints and recalls Assess design and manufacturing changes for 510(k) impact Shape the UK and EU MDR strategy as the business grows Grow the regulatory function over time, including budgets, consultants and, in time, a team What you ll bring 6-7+ years regulatory affairs experience in medical devices Hands-on authorship of at least one successful FDA 510(k) Direct FDA interaction experience, such as Pre-Subs and AI responses Working knowledge of 21 CFR 820 (QMSR), ISO 13485 and ISO 14971 Experience with active or electromechanical Class II/III devices (IEC 60601, IEC 62304) is a strong plus EU MDR and RAC are a bonus Comfortable in a small, fast-moving team where you ll be hands-on Right to work in the UK (sponsorship is not available) Why it s worth a look You ll own regulatory strategy at the most important point in the company s life: FDA submission and US launch A direct line to the CEO, with real influence on the business Equity through share options Occasional US and European travel
Job Title: Scientist 1 - Stability Contract: Jan-Dec Location: Deeside Pay: 122.62pd SRG are partnered with a global medical products and technologies company. Our client is focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care. We are seeking a Scientist to join their Deeside team. Duties and Responsibilities : To perform physical and analytical stability testing on existing and new medical devices and skin care products according to pre-determined stability study protocols, SOPs, OCIs and TDs in support of product shelf-life and product labelling. Analysing, documenting, interpreting, and reporting laboratory data for stability studies to GMP/GLP standards. Perform maintenance, calibration, documentation and updating quality records for Stability equipment. Maintain compliance to ISO13485 & ISO9001 standards in accordance with GLP/GMP compliant procedures. Provide technical knowledge to some stability studies with support from Senior Scientist. Experience with a wide range of analytical equipment such as balances and pipettes through to HPLC and ICP-MS. Performs Lab/OOS investigations with some supervision incorporating problem-solving and troubleshooting for future improvements. Responsible for the ordering of laboratory consumables, chemicals, reagents, and equipment when required. Assist with the drafting of stability documentation such as protocols and reports. Ensure the Stability labs are maintained as a safe working environment, raising near misses where needed. Support planned and ad-hoc stability sample set-downs, pull requests and support laboratory tasks as and when required. Collation of stability data, including physical data retrieval, for stability/technical reports. Assist in the storage and retrieval of stability samples. Liaise with external vendors via telephone and when on site and arrange maintenance, service, and calibration contracts. Support the organisation of new and existing studies including sample retrieval. Support appropriate accelerated and real-time aging programmes that are suitable for the study in concept. Actively generate improvement ideas (Lean/6S) for the Stability laboratories and suite. Identify improvements to current stability processes. Requirements Qualifications/Education: BSc. or equivalent in a scientific discipline (e.g., Chemistry, Biology). Skills & Experience: Lab experience is desirable Basic experience in the utilisation of computerised systems to manage data and information. Ability to react and respond positively to changes in priority and workload. Competent in following and adhering to pre-determined stability study protocols, SOPs, OCIs and TDs. An active team player disciplined in adhering to group objectives including taking an active role in team collaborative activities. Good working knowledge of Microsoft Office - specifically Word and Excel. Understanding of compliance with FDA and European Regulations (ICH), Quality Systems and GMP Guidelines. Proactive and positive mindset with an attitude that is open to change to embrace new ways of working and improvements. Competent in the disposal of chemicals, reagents and solvents in accordance to site and environmental procedures Guidant, Carbon60, Lorien & SRG - The Vertage Group Portfolio are acting as an Employment Business in relation to this vacancy.
Nov 11, 2026
Seasonal
Job Title: Scientist 1 - Stability Contract: Jan-Dec Location: Deeside Pay: 122.62pd SRG are partnered with a global medical products and technologies company. Our client is focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care. We are seeking a Scientist to join their Deeside team. Duties and Responsibilities : To perform physical and analytical stability testing on existing and new medical devices and skin care products according to pre-determined stability study protocols, SOPs, OCIs and TDs in support of product shelf-life and product labelling. Analysing, documenting, interpreting, and reporting laboratory data for stability studies to GMP/GLP standards. Perform maintenance, calibration, documentation and updating quality records for Stability equipment. Maintain compliance to ISO13485 & ISO9001 standards in accordance with GLP/GMP compliant procedures. Provide technical knowledge to some stability studies with support from Senior Scientist. Experience with a wide range of analytical equipment such as balances and pipettes through to HPLC and ICP-MS. Performs Lab/OOS investigations with some supervision incorporating problem-solving and troubleshooting for future improvements. Responsible for the ordering of laboratory consumables, chemicals, reagents, and equipment when required. Assist with the drafting of stability documentation such as protocols and reports. Ensure the Stability labs are maintained as a safe working environment, raising near misses where needed. Support planned and ad-hoc stability sample set-downs, pull requests and support laboratory tasks as and when required. Collation of stability data, including physical data retrieval, for stability/technical reports. Assist in the storage and retrieval of stability samples. Liaise with external vendors via telephone and when on site and arrange maintenance, service, and calibration contracts. Support the organisation of new and existing studies including sample retrieval. Support appropriate accelerated and real-time aging programmes that are suitable for the study in concept. Actively generate improvement ideas (Lean/6S) for the Stability laboratories and suite. Identify improvements to current stability processes. Requirements Qualifications/Education: BSc. or equivalent in a scientific discipline (e.g., Chemistry, Biology). Skills & Experience: Lab experience is desirable Basic experience in the utilisation of computerised systems to manage data and information. Ability to react and respond positively to changes in priority and workload. Competent in following and adhering to pre-determined stability study protocols, SOPs, OCIs and TDs. An active team player disciplined in adhering to group objectives including taking an active role in team collaborative activities. Good working knowledge of Microsoft Office - specifically Word and Excel. Understanding of compliance with FDA and European Regulations (ICH), Quality Systems and GMP Guidelines. Proactive and positive mindset with an attitude that is open to change to embrace new ways of working and improvements. Competent in the disposal of chemicals, reagents and solvents in accordance to site and environmental procedures Guidant, Carbon60, Lorien & SRG - The Vertage Group Portfolio are acting as an Employment Business in relation to this vacancy.
Job Opportunity: Senior LCMS Scientist Salary : 30,000 - 38,000 Location : Cheshire, UK Type : Permanent Overview Join our team as a Senior LCMS Scientist, making key contributions to pharmaceutical product development through analytical excellence using Liquid Chromatography-Mass Spectrometry (LCMS). Key Responsibilities Lead LCMS activities across drug development stages. Develop, optimize, and validate LCMS methods. Resolve complex LCMS challenges. Collaborate with multidisciplinary teams to achieve project goals. Ensure compliance with regulatory standards for method validation. Analyze LCMS data, create reports, and present findings. Innovate and improve LCMS methodologies. Qualifications Degree (BSc, MSc, PhD) in Analytical Chemistry, Chemistry, or related field. Extensive LCMS experience, preferably in pharmaceutical analysis. Proven expertise in developing and troubleshooting LCMS methods for APIs and raw materials. Strong communication skills to convey complex data effectively. Proficiency with software like Empower or UNIFI (advantageous). Benefits Salary: 30,000 - 38,000 Company pension scheme Health and life insurance Apply Now Note : Applicants must have the right to work in the UK. Visa sponsorship not available. We are an Equal Opportunities Employer committed to fostering inclusivity.
Nov 10, 2026
Full time
Job Opportunity: Senior LCMS Scientist Salary : 30,000 - 38,000 Location : Cheshire, UK Type : Permanent Overview Join our team as a Senior LCMS Scientist, making key contributions to pharmaceutical product development through analytical excellence using Liquid Chromatography-Mass Spectrometry (LCMS). Key Responsibilities Lead LCMS activities across drug development stages. Develop, optimize, and validate LCMS methods. Resolve complex LCMS challenges. Collaborate with multidisciplinary teams to achieve project goals. Ensure compliance with regulatory standards for method validation. Analyze LCMS data, create reports, and present findings. Innovate and improve LCMS methodologies. Qualifications Degree (BSc, MSc, PhD) in Analytical Chemistry, Chemistry, or related field. Extensive LCMS experience, preferably in pharmaceutical analysis. Proven expertise in developing and troubleshooting LCMS methods for APIs and raw materials. Strong communication skills to convey complex data effectively. Proficiency with software like Empower or UNIFI (advantageous). Benefits Salary: 30,000 - 38,000 Company pension scheme Health and life insurance Apply Now Note : Applicants must have the right to work in the UK. Visa sponsorship not available. We are an Equal Opportunities Employer committed to fostering inclusivity.
Principal Scientist - Analytical Overview A global pharmaceutical organisation are seeking a Principal Scientist to join their analytical development team in a state-of-the-art facility supporting cutting-edge API development. This is an excellent opportunity for an individual looking to advance their career in analytical chemistry with broad responsibilties across AD, project management and commercial activites. Responsibilities Collaborate with cross-functional teams to support drug substance process research and development. Develop and implement innovative analytical strategies to enhance operational efficiency and deliver high-quality results. Ensure compliance with industry standards, regulations, and company policies specific to analytical methodologies and practices. Provide scientific leadership and mentorship to team members, fostering a culture of technical excellence and continuous learning. Analyse complex datasets and generate comprehensive reports to support decision-making processes. Identify opportunities for growth, innovation, and process improvement within the analytical sciences space. Qualifications Proven experience as a Principal Scientist or in a similar scientific role, demonstrating a strong track record of success in analytical sciences. Strong expertise in analytical techniques, problem-solving, and method development. Excellent communication, leadership, and collaboration skills. Ability to independently manage complex projects and collaborate effectively with multidisciplinary teams. Proficiency in advanced analytical tools and relevant software. A degree (PhD preferred) in chemistry, biochemistry, analytical sciences, or a related field is required. Benefits Competitive salary of up to 57K. Opportunities for professional development and career progression in advanced analytical sciences. A supportive and inclusive work environment that values innovation and excellence. Access to a state-of-the-art facility equipped with the latest technology to facilitate your work. Comprehensive benefits package, including pension contributions and health coverage. Flexible working arrangements to promote work-life balance. If you are an experienced and results-driven professional specialising in analytical sciences, we encourage you to apply for this exciting opportunity. Join us to contribute your expertise, work in a modern research environment, and take the next significant step in your career.
Nov 10, 2026
Full time
Principal Scientist - Analytical Overview A global pharmaceutical organisation are seeking a Principal Scientist to join their analytical development team in a state-of-the-art facility supporting cutting-edge API development. This is an excellent opportunity for an individual looking to advance their career in analytical chemistry with broad responsibilties across AD, project management and commercial activites. Responsibilities Collaborate with cross-functional teams to support drug substance process research and development. Develop and implement innovative analytical strategies to enhance operational efficiency and deliver high-quality results. Ensure compliance with industry standards, regulations, and company policies specific to analytical methodologies and practices. Provide scientific leadership and mentorship to team members, fostering a culture of technical excellence and continuous learning. Analyse complex datasets and generate comprehensive reports to support decision-making processes. Identify opportunities for growth, innovation, and process improvement within the analytical sciences space. Qualifications Proven experience as a Principal Scientist or in a similar scientific role, demonstrating a strong track record of success in analytical sciences. Strong expertise in analytical techniques, problem-solving, and method development. Excellent communication, leadership, and collaboration skills. Ability to independently manage complex projects and collaborate effectively with multidisciplinary teams. Proficiency in advanced analytical tools and relevant software. A degree (PhD preferred) in chemistry, biochemistry, analytical sciences, or a related field is required. Benefits Competitive salary of up to 57K. Opportunities for professional development and career progression in advanced analytical sciences. A supportive and inclusive work environment that values innovation and excellence. Access to a state-of-the-art facility equipped with the latest technology to facilitate your work. Comprehensive benefits package, including pension contributions and health coverage. Flexible working arrangements to promote work-life balance. If you are an experienced and results-driven professional specialising in analytical sciences, we encourage you to apply for this exciting opportunity. Join us to contribute your expertise, work in a modern research environment, and take the next significant step in your career.
STEM Recruitment is seeking a skilled Application Scientist to join our client s innovative team based in Glasgow and Strathclyde, Scotland. The ideal candidate will have a strong chemistry background, with experience in food manufacturing, and expertise in hydrogel, collagen, colloid, and gel-based systems. Your role will involve developing scientific insights into the behaviour of casings and gels in customer applications, collaborating with material scientists and process engineers, and delivering technical solutions for product development. This position demands hands-on scientific work, creativity, and proactive collaboration to enable product and technology innovation. Master s or PhD in Chemical Engineering, Food Technology, or related fields At least three years experience in research, product development or technical applications Experience working with hydrogels, collagen, colloids, and related systems in a lab or pilot setting Strong analytical and scientific insight skills Experience in food manufacturing or sausage production is desirable Benefits include an annual bonus, 8% pension match, and x5 life assurance. This is a permanent full-time role offering the chance to work within a dynamic team focused on innovation and scientific excellence in a supportive environment.
Nov 09, 2026
Full time
STEM Recruitment is seeking a skilled Application Scientist to join our client s innovative team based in Glasgow and Strathclyde, Scotland. The ideal candidate will have a strong chemistry background, with experience in food manufacturing, and expertise in hydrogel, collagen, colloid, and gel-based systems. Your role will involve developing scientific insights into the behaviour of casings and gels in customer applications, collaborating with material scientists and process engineers, and delivering technical solutions for product development. This position demands hands-on scientific work, creativity, and proactive collaboration to enable product and technology innovation. Master s or PhD in Chemical Engineering, Food Technology, or related fields At least three years experience in research, product development or technical applications Experience working with hydrogels, collagen, colloids, and related systems in a lab or pilot setting Strong analytical and scientific insight skills Experience in food manufacturing or sausage production is desirable Benefits include an annual bonus, 8% pension match, and x5 life assurance. This is a permanent full-time role offering the chance to work within a dynamic team focused on innovation and scientific excellence in a supportive environment.
Job Title: Safety Data Transformation Lead / Specialist Location: Welwyn (Hybrid) Hourly Rate: 29.85 - 35.82 PAYE ( 40 - 48 Umb) Our client, a leading organisation in the pharmaceutical industry, is seeking a dynamic and experienced Safety Data Transformation Lead / Specialist to join their Patient Safety Operations - Data Transformation team. This is a unique opportunity to leverage your pharmacovigilance expertise and play a pivotal role in ensuring the highest standards of safety data processing and reporting. Key Responsibilities: As a Safety Data Transformation Lead / Specialist, your daily tasks will include: Overseeing service providers executing Individual Case Safety Report (ICSR) tasks and medical device reports. Proactively answering queries and sharing your subject matter expertise with stakeholders, including business partners, auditors, and inspectors. Conducting process reviews to design and implement process improvements that enhance quality and compliance. Identifying root causes of non-compliance and agreeing on Corrective Actions and Preventative Actions (CAPAs), with responsibility for implementation. Assessing the impact of new or updated regulatory requirements on your area of expertise. Qualifications and Experience: Our client is looking for candidates with: A foundational educational background, such as an undergraduate degree, or equivalent on-the-job pharmacovigilance experience. Demonstrated experience in various areas of pharmacovigilance and an understanding of international regulations (ICH, EU GVP Modules, FDA). A good grasp of the pharmaceutical industry and the rapidly evolving personalised healthcare landscape. Medical device processing experience is desirable but not mandatory. Ideal Candidate Attributes: The organisation seeks individuals who embody the following traits: Profound Knowledge: In-depth understanding of ICSR case processing and broad knowledge of the end-to-end ICSR process. Accountable Leadership: A proactive leader who is self-motivated and excels in process development and issue management. Quality Mindset: Maintains procedural documents, devises strategies to mitigate risks, and transparently escalates issues. Effective Oversight: Skilled at relationship management and capable of analysing metrics to ensure service quality. Strong Communicator: Ability to influence colleagues and articulate processes to external stakeholders, particularly during regulatory inspections. Critical Thinker: Can connect processes, data, and ideas to see the bigger picture and create impactful solutions. Adaptable Team Player: Open and supportive in both co-located and virtual teams, capable of managing ambiguity and reprioritising tasks. This role is an excellent opportunity for those who are passionate about patient safety and eager to make a meaningful impact within the pharmaceutical sector. If you possess the required skills and experience, this could be the perfect position for you! Apply Now! Our client is excited to meet candidates who are ready to step into this vital role. If you are driven by a commitment to excellence in patient safety and possess the necessary qualifications, please submit your application today! Note: Only shortlisted candidates will be contacted. We use generative AI tools to support our candidate screening process. This helps us ensure a fair, consistent, and efficient experience for all applicants. Rest assured, all final decisions are made by our hiring team, and your application will be reviewed with care and attention. Adecco is a disability-confident employer. It is important to us that we run an inclusive and accessible recruitment process to support candidates of all backgrounds and all abilities to apply. Adecco is committed to building a supportive environment for you to explore the next steps in your career. If you require reasonable adjustments at any stage, please let us know and we will be happy to support you.
Nov 09, 2026
Contractor
Job Title: Safety Data Transformation Lead / Specialist Location: Welwyn (Hybrid) Hourly Rate: 29.85 - 35.82 PAYE ( 40 - 48 Umb) Our client, a leading organisation in the pharmaceutical industry, is seeking a dynamic and experienced Safety Data Transformation Lead / Specialist to join their Patient Safety Operations - Data Transformation team. This is a unique opportunity to leverage your pharmacovigilance expertise and play a pivotal role in ensuring the highest standards of safety data processing and reporting. Key Responsibilities: As a Safety Data Transformation Lead / Specialist, your daily tasks will include: Overseeing service providers executing Individual Case Safety Report (ICSR) tasks and medical device reports. Proactively answering queries and sharing your subject matter expertise with stakeholders, including business partners, auditors, and inspectors. Conducting process reviews to design and implement process improvements that enhance quality and compliance. Identifying root causes of non-compliance and agreeing on Corrective Actions and Preventative Actions (CAPAs), with responsibility for implementation. Assessing the impact of new or updated regulatory requirements on your area of expertise. Qualifications and Experience: Our client is looking for candidates with: A foundational educational background, such as an undergraduate degree, or equivalent on-the-job pharmacovigilance experience. Demonstrated experience in various areas of pharmacovigilance and an understanding of international regulations (ICH, EU GVP Modules, FDA). A good grasp of the pharmaceutical industry and the rapidly evolving personalised healthcare landscape. Medical device processing experience is desirable but not mandatory. Ideal Candidate Attributes: The organisation seeks individuals who embody the following traits: Profound Knowledge: In-depth understanding of ICSR case processing and broad knowledge of the end-to-end ICSR process. Accountable Leadership: A proactive leader who is self-motivated and excels in process development and issue management. Quality Mindset: Maintains procedural documents, devises strategies to mitigate risks, and transparently escalates issues. Effective Oversight: Skilled at relationship management and capable of analysing metrics to ensure service quality. Strong Communicator: Ability to influence colleagues and articulate processes to external stakeholders, particularly during regulatory inspections. Critical Thinker: Can connect processes, data, and ideas to see the bigger picture and create impactful solutions. Adaptable Team Player: Open and supportive in both co-located and virtual teams, capable of managing ambiguity and reprioritising tasks. This role is an excellent opportunity for those who are passionate about patient safety and eager to make a meaningful impact within the pharmaceutical sector. If you possess the required skills and experience, this could be the perfect position for you! Apply Now! Our client is excited to meet candidates who are ready to step into this vital role. If you are driven by a commitment to excellence in patient safety and possess the necessary qualifications, please submit your application today! Note: Only shortlisted candidates will be contacted. We use generative AI tools to support our candidate screening process. This helps us ensure a fair, consistent, and efficient experience for all applicants. Rest assured, all final decisions are made by our hiring team, and your application will be reviewed with care and attention. Adecco is a disability-confident employer. It is important to us that we run an inclusive and accessible recruitment process to support candidates of all backgrounds and all abilities to apply. Adecco is committed to building a supportive environment for you to explore the next steps in your career. If you require reasonable adjustments at any stage, please let us know and we will be happy to support you.
Senior Scientist Immunology / Inflammation Research Location: Oxford Contract: 12 months Rate: £54.00 to £57.00 per hour / £405.00 to £427.00 per day (via Umbrella) The Opportunity: ISR Recruitment is supporting a leading global biopharmaceutical organisation seeking an experienced Senior Scientist to contribute to the discovery of novel biologic therapies for autoimmune diseases. This is an exciting, laboratory-based research opportunity for a scientifically curious immunologist with strong experimental skills, a passion for inflammation research and an interest in advancing innovative therapeutics. Role and Responsibilities: Design, develop and perform robust in vitro assays to investigate immune responses and support therapeutic antibody discovery. Conduct hands-on laboratory work, including primary immune cell isolation and culture, cell line engineering and multicolour flow cytometry. Analyse, interpret and present experimental data, drawing clear scientific conclusions and troubleshooting challenges. Maintain accurate electronic laboratory records and ensure high standards of scientific rigour. Collaborate with internal research teams, external experts, CROs and academic partners to deliver R&D programmes. Contribute to project planning, scientific discussions, research publications and patent applications. Skills and Experience: PhD in Life Sciences, Immunology or a related discipline, with at least three years relevant research experience. Strong understanding of immunology, inflammation and autoimmune disease biology. Practical experience assessing immune responses using relevant cellular and laboratory techniques. Excellent experimental design, data analysis and troubleshooting skills. Strong communication, organisation and teamwork skills. Desirable: Experience within pharmaceutical or biotechnology drug discovery, particularly preclinical research and biologic therapeutics. Applications: Interested to learn more? If you have hands-on immunology research experience and want to contribute to the development of innovative treatments for autoimmune disease on a temporary contract for an initial 12 months based in the Oxford area; please contact with Edward Laing here at ISR Recruitment to discuss further or please share a copy of your latest CV and / or online business profile for a call back in the strictest of confidence?
Nov 08, 2026
Contractor
Senior Scientist Immunology / Inflammation Research Location: Oxford Contract: 12 months Rate: £54.00 to £57.00 per hour / £405.00 to £427.00 per day (via Umbrella) The Opportunity: ISR Recruitment is supporting a leading global biopharmaceutical organisation seeking an experienced Senior Scientist to contribute to the discovery of novel biologic therapies for autoimmune diseases. This is an exciting, laboratory-based research opportunity for a scientifically curious immunologist with strong experimental skills, a passion for inflammation research and an interest in advancing innovative therapeutics. Role and Responsibilities: Design, develop and perform robust in vitro assays to investigate immune responses and support therapeutic antibody discovery. Conduct hands-on laboratory work, including primary immune cell isolation and culture, cell line engineering and multicolour flow cytometry. Analyse, interpret and present experimental data, drawing clear scientific conclusions and troubleshooting challenges. Maintain accurate electronic laboratory records and ensure high standards of scientific rigour. Collaborate with internal research teams, external experts, CROs and academic partners to deliver R&D programmes. Contribute to project planning, scientific discussions, research publications and patent applications. Skills and Experience: PhD in Life Sciences, Immunology or a related discipline, with at least three years relevant research experience. Strong understanding of immunology, inflammation and autoimmune disease biology. Practical experience assessing immune responses using relevant cellular and laboratory techniques. Excellent experimental design, data analysis and troubleshooting skills. Strong communication, organisation and teamwork skills. Desirable: Experience within pharmaceutical or biotechnology drug discovery, particularly preclinical research and biologic therapeutics. Applications: Interested to learn more? If you have hands-on immunology research experience and want to contribute to the development of innovative treatments for autoimmune disease on a temporary contract for an initial 12 months based in the Oxford area; please contact with Edward Laing here at ISR Recruitment to discuss further or please share a copy of your latest CV and / or online business profile for a call back in the strictest of confidence?
Talentmark are recruiting for a Senior Scientist/Associate Principal Scientist - Process Chemistry on behalf of a growing drug development partner who support clients across the pharmaceutical and biotech sectors. This role will be based in Cardiff, on a permanent basis. Responsibilities: Working collaboratively on a range of client programmes, applying technical expertise to solve challenging problems across drug discovery and development. Technically leading projects/work packages for our customers, under the guidance of a senior manager. Designing experimental work for yourself, and other scientists (as required), conducting laboratory work and interpreting results to draw conclusions. Applying scientific judgement to troubleshoot and solve technical challenges. Delivering project milestones to agreed timelines and quality standards. Presenting data clearly to project teams and clients, both written and verbal. Supporting and mentoring more junior Scientists. Maintaining excellent standards of documentation, data integrity, and laboratory safety. Your Background: Educated to MSc or PhD level in a relevant chemistry field. Significant relevant industry experience in process chemistry in drug discovery. Experience with late-stage process optimisation, encompassing activities such as impurity fate and purge, PAR/NOR studies, robustness studies, technology transfer and/or support of manufacturing campaigns. Experience in a CRO environment would be beneficial. Strong experimental design and data interpretation skills. The ability to work independently while contributing effectively to teams. Apply: It is essential all applicants hold entitlement to work in the UK. Please quote job reference 71494 in all correspondence.
Nov 08, 2026
Full time
Talentmark are recruiting for a Senior Scientist/Associate Principal Scientist - Process Chemistry on behalf of a growing drug development partner who support clients across the pharmaceutical and biotech sectors. This role will be based in Cardiff, on a permanent basis. Responsibilities: Working collaboratively on a range of client programmes, applying technical expertise to solve challenging problems across drug discovery and development. Technically leading projects/work packages for our customers, under the guidance of a senior manager. Designing experimental work for yourself, and other scientists (as required), conducting laboratory work and interpreting results to draw conclusions. Applying scientific judgement to troubleshoot and solve technical challenges. Delivering project milestones to agreed timelines and quality standards. Presenting data clearly to project teams and clients, both written and verbal. Supporting and mentoring more junior Scientists. Maintaining excellent standards of documentation, data integrity, and laboratory safety. Your Background: Educated to MSc or PhD level in a relevant chemistry field. Significant relevant industry experience in process chemistry in drug discovery. Experience with late-stage process optimisation, encompassing activities such as impurity fate and purge, PAR/NOR studies, robustness studies, technology transfer and/or support of manufacturing campaigns. Experience in a CRO environment would be beneficial. Strong experimental design and data interpretation skills. The ability to work independently while contributing effectively to teams. Apply: It is essential all applicants hold entitlement to work in the UK. Please quote job reference 71494 in all correspondence.
Talentmark are recruiting for a Downstream Processing Scientist to join a company in the animal health and pharmaceutical industry on a contract basis for 6 months. This role is fully site-based in Speke, Merseyside. Company: Our client specialises in animal health. They advance their vision of food and companionship, enriching life by developing innovative solutions that protect and enhance animal health. Salary: From 15.38 to 20.51 ph PAYE Rates are dependant upon experience Downstream Processing Scientist Role: Plan and execute laboratory and pilot-scale studies through hands-on experimentation. Deliver downstream purification processes to support clinical programs and business milestones. Utilise statistical tools to design, analyse, and interpret complex data sets. Provide technical and operational expertise in downstream processing. Support the maintenance and readiness of downstream laboratory equipment. Your Background : Hold a relevant scientific degree, or have equivalent working experience. Some previous experience in biopharmaceutical downstream development or manufacturing. Familiarity with a range of techiques/sytems such as the following would be an advantage: FPLC Chromatography (AKTA systems with Unicorn Software) Familiarity with GxP Standards. Depth Filtration Process Scale Up Apply: For more information, or to apply for this Downstream Processing Scientist , please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference 71491. It is essential that applicants hold entitlement to work in the UK Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
Nov 08, 2026
Contractor
Talentmark are recruiting for a Downstream Processing Scientist to join a company in the animal health and pharmaceutical industry on a contract basis for 6 months. This role is fully site-based in Speke, Merseyside. Company: Our client specialises in animal health. They advance their vision of food and companionship, enriching life by developing innovative solutions that protect and enhance animal health. Salary: From 15.38 to 20.51 ph PAYE Rates are dependant upon experience Downstream Processing Scientist Role: Plan and execute laboratory and pilot-scale studies through hands-on experimentation. Deliver downstream purification processes to support clinical programs and business milestones. Utilise statistical tools to design, analyse, and interpret complex data sets. Provide technical and operational expertise in downstream processing. Support the maintenance and readiness of downstream laboratory equipment. Your Background : Hold a relevant scientific degree, or have equivalent working experience. Some previous experience in biopharmaceutical downstream development or manufacturing. Familiarity with a range of techiques/sytems such as the following would be an advantage: FPLC Chromatography (AKTA systems with Unicorn Software) Familiarity with GxP Standards. Depth Filtration Process Scale Up Apply: For more information, or to apply for this Downstream Processing Scientist , please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference 71491. It is essential that applicants hold entitlement to work in the UK Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
Help us to make a world of difference Urenco is a global leader in the production of low-carbon energy, playing a critical role in delivering secure, reliable nuclear fuel solutions worldwide. We are focused on enabling the sustainable generation of electricity for customers around the world while operating to the highest environmental, social, and regulatory standards. In addition, as part of a strategically important industry, Urenco is now required to support the UK Government in exploring options to re-establish nuclear fuel capabilities to produce reactor fuel for defence purposes. To support this new project, we are seeking a Physics Scientist to join our Capenhurst/Birchwood site. In this role, you will work within our Government Services function as a key interface between site teams and Group stakeholders to ensure effective planning, coordination, and delivery across complex programmes. You will provide scientific and technical expertise to support the development, verification, and assurance of advanced process technologies and facility designs. You will contribute to the design and analysis of complex process systems through scientific modelling, simulation, and computational analysis, ensuring solutions meet safety, performance, and operational requirements. Acting as a delegated Design Authority within your area of expertise, you will support new technology development, provide governance and oversight throughout the asset lifecycle, and contribute to the advancement of innovative methodologies, digital solutions, and artificial intelligence applications across Urenco's operations. At Urenco, we're committed to helping you be your best. If you feel you meet some, but not all, of what we're looking for, we still encourage you to apply. We believe in embracing the passion and potential of our people and offer market-leading training, development, coaching, and mentoring opportunities from some of the brightest minds in the industry. What You'll Do Provide Scientific & Technical Leadership Provide scientific analysis and computational modelling to support design development and design assurance activities. Review and approve designs within your area of expertise as delegated Design Authority. Develop and apply innovative methods, tools, and techniques to optimise process performance and safety. Support the application of artificial intelligence and advanced technologies within complex process environments. Support Design Authority & Engineering Assurance Provide governance and oversight of design development, project execution, operations, and decommissioning activities. Establish, maintain, and develop Group Reference Designs and safety case standards. Conduct design reviews and support supplier oversight activities where required. Ensure designs align with regulatory, operational, safety, and business requirements. Drive Safety & Performance Improvement Promote a proactive safety culture and learning-from-experience approach. Ensure plant designs incorporate appropriate safety features and industry best practice. Lead Post Implementation Reviews and support continuous improvement activities. Support safety case development and design substantiation through technical analysis. Provide Specialist Technical Support Carry out troubleshooting and debottlenecking investigations for operational facilities. Analyse complex process and measurement data to identify performance improvements and root causes of events. Support site teams with specialist technical expertise to resolve operational challenges. Provide expert advice on core technology and complex process systems. What Do You Need to Thrive in This Role? Qualifications Master's Degree or PhD in Physics, Mathematics, Mechanical Engineering, Nuclear Science, Advanced Technology, or a related discipline. Experience Recognised specialist within a relevant scientific or technical discipline. Demonstrable experience supporting the design and delivery of complex process facilities. Experience applying scientific methods, modelling, and analysis to engineering challenges. Technical & Professional Capability Strong knowledge of computational physics, mathematics, modelling, and simulation techniques. Ability to analyse complex systems and data to solve technical problems and optimise performance. Experience supporting safety case substantiation, process development, or technology innovation. Strong analytical, problem-solving, and communication skills. Behavioural Attributes Results-focused with a commitment to high performance and quality. Customer-focused and solutions-oriented approach. Strong analytical and decision-making capability. Commitment to safety, innovation, and continuous improvement. What Can You Expect From Us? More than just a job, we offer a future. More than just a place to work, we provide an opportunity to prosper. As a valued member of our team, you will receive: Generous Annual Leave : Starting at 25 days, increasing by one day every two years (up to 30 days), plus 13 additional flexible days. Option to buy or sell up to 5 holiday days. Family-Friendly Policies : A wide range of policies to support work-life balance and family needs. Bonus Scheme : A competitive bonus scheme based on company and individual performance. Pension Scheme : Defined contribution plan with up to 16% employer contribution. Private Medical & Dental Cover : Single cover, with the option to purchase additional benefits. Flexible Benefits : Life assurance, income protection, and benefits tailored to your lifestyle. Training & Development : Personalised learning and development opportunities to support your career growth. Security Vetting Due to the nature of the industry in which Urenco operates, successful candidates will be required to obtain and maintain the appropriate level of security clearance for the role. All offers of employment are subject to satisfactory completion of the required vetting and screening checks. Creating a Diverse and Inclusive Workforce As a truly global organisation with operations in the UK, USA, Germany, and the Netherlands, we know that our differences make us stronger. We are committed to creating an inclusive workplace where everyone feels valued, respected, and empowered to succeed. If you require any reasonable adjustments during the recruitment process, please let our Talent Acquisition team know. Because together, we are One Urenco. We are enriching the world. And enriching your future.
Nov 08, 2026
Full time
Help us to make a world of difference Urenco is a global leader in the production of low-carbon energy, playing a critical role in delivering secure, reliable nuclear fuel solutions worldwide. We are focused on enabling the sustainable generation of electricity for customers around the world while operating to the highest environmental, social, and regulatory standards. In addition, as part of a strategically important industry, Urenco is now required to support the UK Government in exploring options to re-establish nuclear fuel capabilities to produce reactor fuel for defence purposes. To support this new project, we are seeking a Physics Scientist to join our Capenhurst/Birchwood site. In this role, you will work within our Government Services function as a key interface between site teams and Group stakeholders to ensure effective planning, coordination, and delivery across complex programmes. You will provide scientific and technical expertise to support the development, verification, and assurance of advanced process technologies and facility designs. You will contribute to the design and analysis of complex process systems through scientific modelling, simulation, and computational analysis, ensuring solutions meet safety, performance, and operational requirements. Acting as a delegated Design Authority within your area of expertise, you will support new technology development, provide governance and oversight throughout the asset lifecycle, and contribute to the advancement of innovative methodologies, digital solutions, and artificial intelligence applications across Urenco's operations. At Urenco, we're committed to helping you be your best. If you feel you meet some, but not all, of what we're looking for, we still encourage you to apply. We believe in embracing the passion and potential of our people and offer market-leading training, development, coaching, and mentoring opportunities from some of the brightest minds in the industry. What You'll Do Provide Scientific & Technical Leadership Provide scientific analysis and computational modelling to support design development and design assurance activities. Review and approve designs within your area of expertise as delegated Design Authority. Develop and apply innovative methods, tools, and techniques to optimise process performance and safety. Support the application of artificial intelligence and advanced technologies within complex process environments. Support Design Authority & Engineering Assurance Provide governance and oversight of design development, project execution, operations, and decommissioning activities. Establish, maintain, and develop Group Reference Designs and safety case standards. Conduct design reviews and support supplier oversight activities where required. Ensure designs align with regulatory, operational, safety, and business requirements. Drive Safety & Performance Improvement Promote a proactive safety culture and learning-from-experience approach. Ensure plant designs incorporate appropriate safety features and industry best practice. Lead Post Implementation Reviews and support continuous improvement activities. Support safety case development and design substantiation through technical analysis. Provide Specialist Technical Support Carry out troubleshooting and debottlenecking investigations for operational facilities. Analyse complex process and measurement data to identify performance improvements and root causes of events. Support site teams with specialist technical expertise to resolve operational challenges. Provide expert advice on core technology and complex process systems. What Do You Need to Thrive in This Role? Qualifications Master's Degree or PhD in Physics, Mathematics, Mechanical Engineering, Nuclear Science, Advanced Technology, or a related discipline. Experience Recognised specialist within a relevant scientific or technical discipline. Demonstrable experience supporting the design and delivery of complex process facilities. Experience applying scientific methods, modelling, and analysis to engineering challenges. Technical & Professional Capability Strong knowledge of computational physics, mathematics, modelling, and simulation techniques. Ability to analyse complex systems and data to solve technical problems and optimise performance. Experience supporting safety case substantiation, process development, or technology innovation. Strong analytical, problem-solving, and communication skills. Behavioural Attributes Results-focused with a commitment to high performance and quality. Customer-focused and solutions-oriented approach. Strong analytical and decision-making capability. Commitment to safety, innovation, and continuous improvement. What Can You Expect From Us? More than just a job, we offer a future. More than just a place to work, we provide an opportunity to prosper. As a valued member of our team, you will receive: Generous Annual Leave : Starting at 25 days, increasing by one day every two years (up to 30 days), plus 13 additional flexible days. Option to buy or sell up to 5 holiday days. Family-Friendly Policies : A wide range of policies to support work-life balance and family needs. Bonus Scheme : A competitive bonus scheme based on company and individual performance. Pension Scheme : Defined contribution plan with up to 16% employer contribution. Private Medical & Dental Cover : Single cover, with the option to purchase additional benefits. Flexible Benefits : Life assurance, income protection, and benefits tailored to your lifestyle. Training & Development : Personalised learning and development opportunities to support your career growth. Security Vetting Due to the nature of the industry in which Urenco operates, successful candidates will be required to obtain and maintain the appropriate level of security clearance for the role. All offers of employment are subject to satisfactory completion of the required vetting and screening checks. Creating a Diverse and Inclusive Workforce As a truly global organisation with operations in the UK, USA, Germany, and the Netherlands, we know that our differences make us stronger. We are committed to creating an inclusive workplace where everyone feels valued, respected, and empowered to succeed. If you require any reasonable adjustments during the recruitment process, please let our Talent Acquisition team know. Because together, we are One Urenco. We are enriching the world. And enriching your future.
Our client is a world-renowned, global healthcare and medical device manufacturer with a major state-of-the-art facility based in Witney. Known for their life-changing medical technologies, they offer an incredibly stable, supportive, and structured working environment We are looking for graduate or early career scientist. Some experience in industry is preferable but not essential. Role : Scientist Location : Witney Salary: 30,000 p.a- 35,000 p.a Work hours : 37.5 hours a week Job type: 12 Months Roles and Responsibilities Perform testing to protocol or procedure whilst adhering to good laboratory practice Develop protocols to accomplish goals Produce prototype product or communicate protoype requirements to support experiments. Utilise analytical instruments and train others in their operation Participate in experimental design discussions, identify variables that may impact experimental results Analyse data, evaluate results and form conclusions Prepares effective summaries of results and communicates these to wider team Compile and maintain records as required by good laboratory practice Writes clear and technically correct reports with feedback from colleagues Liase with other departments and present technical information to team meetings Have awareness of change control procedures applicable to role Know and apply knowledge of health and safety procedures Responsible for own laboratory notebook and for the accuracy, quality and timeliness of experimental results Ensures that all work complies with the quality system Uses scientific and industry literature to broaden technical and theoretical understanding Highlights improvement opportunities to manager Basic Qualifications Good written and oral communication skills Good working knowledge of software packages such as Word, Excel and Powerpoint to analyse data, present results and write reports Experience of working in a laboratory, scientific or technical environment Randstad Business Support is acting as an Employment Business in relation to this vacancy.
Nov 08, 2026
Contractor
Our client is a world-renowned, global healthcare and medical device manufacturer with a major state-of-the-art facility based in Witney. Known for their life-changing medical technologies, they offer an incredibly stable, supportive, and structured working environment We are looking for graduate or early career scientist. Some experience in industry is preferable but not essential. Role : Scientist Location : Witney Salary: 30,000 p.a- 35,000 p.a Work hours : 37.5 hours a week Job type: 12 Months Roles and Responsibilities Perform testing to protocol or procedure whilst adhering to good laboratory practice Develop protocols to accomplish goals Produce prototype product or communicate protoype requirements to support experiments. Utilise analytical instruments and train others in their operation Participate in experimental design discussions, identify variables that may impact experimental results Analyse data, evaluate results and form conclusions Prepares effective summaries of results and communicates these to wider team Compile and maintain records as required by good laboratory practice Writes clear and technically correct reports with feedback from colleagues Liase with other departments and present technical information to team meetings Have awareness of change control procedures applicable to role Know and apply knowledge of health and safety procedures Responsible for own laboratory notebook and for the accuracy, quality and timeliness of experimental results Ensures that all work complies with the quality system Uses scientific and industry literature to broaden technical and theoretical understanding Highlights improvement opportunities to manager Basic Qualifications Good written and oral communication skills Good working knowledge of software packages such as Word, Excel and Powerpoint to analyse data, present results and write reports Experience of working in a laboratory, scientific or technical environment Randstad Business Support is acting as an Employment Business in relation to this vacancy.
Exciting new opportunity for an experienced and analytically minded Study Director seeking career progression with an internationally renowned and expanding Biopharmaceutical Laboratory! In this diverse, multifaceted position, you will call upon your expertise in regulated studies to undertake a broad range of challenging bioanalytical projects for several world-leading organisations. Acting as a scientific point of contact for both internal teams and external clients, your work will focus on the oversight, management, and strategic direction of studies supporting PK, ADA and biomarker analysis, ensuring delivery to the highest scientific and regulatory standards. The ideal candidate will have: A relevant degree (BSc/MSc in Biology or related field) Specialist knowledge & experience in bioanalytical techniques, particularly within PK, Anti-drug Antibody (ADA) & Biomarker studies Proven experience working to GCP and GLP regulations, including managing and directing regulated studies Excellent written and verbal communication skills, with the ability to act as a scientific point of contact Strong work ethic and drive to learn Candidates with strong experience in either regulated work or biological work are encouraged to apply, as training can be provided for the complementary skill set This is an excellent opportunity to join a respected organisation, where scientific quality, collaboration, and professional development are genuinely valued. Please apply now to VRS recruitment to find out more!
Nov 08, 2026
Full time
Exciting new opportunity for an experienced and analytically minded Study Director seeking career progression with an internationally renowned and expanding Biopharmaceutical Laboratory! In this diverse, multifaceted position, you will call upon your expertise in regulated studies to undertake a broad range of challenging bioanalytical projects for several world-leading organisations. Acting as a scientific point of contact for both internal teams and external clients, your work will focus on the oversight, management, and strategic direction of studies supporting PK, ADA and biomarker analysis, ensuring delivery to the highest scientific and regulatory standards. The ideal candidate will have: A relevant degree (BSc/MSc in Biology or related field) Specialist knowledge & experience in bioanalytical techniques, particularly within PK, Anti-drug Antibody (ADA) & Biomarker studies Proven experience working to GCP and GLP regulations, including managing and directing regulated studies Excellent written and verbal communication skills, with the ability to act as a scientific point of contact Strong work ethic and drive to learn Candidates with strong experience in either regulated work or biological work are encouraged to apply, as training can be provided for the complementary skill set This is an excellent opportunity to join a respected organisation, where scientific quality, collaboration, and professional development are genuinely valued. Please apply now to VRS recruitment to find out more!
Role : Operations scientist Location : Witney Salary: 33,500 p.a Work hours : 37.5 hours a week Job type: 6 Months Client: Abbott Roles and Responsibilities Perform testing to protocol or procedure whilst adhering to good laboratory practice Develop protocols to accomplish goals Produce prototype product or communicate protoype requirements to support experiments. Utilise analytical instruments and train others in their operation Participate in experimental design discussions, identify variables that may impact experimental results Analyse data, evaluate results and form conclusions Prepares effective summaries of results and communicates these to wider team Compile and maintain records as required by good laboratory practice Writes clear and technically correct reports with feedback from colleagues Liase with other departments and present technical information to team meetings Have awareness of change control procedures applicable to role Know and apply knowledge of health and safety procedures Responsible for own laboratory notebook and for the accuracy, quality and timeliness of experimental results Ensures that all work complies with the quality system Uses scientific and industry literature to broaden technical and theoretical understanding Highlights improvement opportunities to manager Consistently demonstrates recognised behaviours Basic Qualifications A Levels ( 16 years) STEM subjects desirable but not required Experience of working in a laboratory, scientific or technical environment or other relevant industry Experience of writing technical reports and presenting results Limited technical knowledge Good working knowledge of software packages such as Word, Excel, PowerPoint Randstad Business Support is acting as an Employment Business in relation to this vacancy.
Nov 08, 2026
Contractor
Role : Operations scientist Location : Witney Salary: 33,500 p.a Work hours : 37.5 hours a week Job type: 6 Months Client: Abbott Roles and Responsibilities Perform testing to protocol or procedure whilst adhering to good laboratory practice Develop protocols to accomplish goals Produce prototype product or communicate protoype requirements to support experiments. Utilise analytical instruments and train others in their operation Participate in experimental design discussions, identify variables that may impact experimental results Analyse data, evaluate results and form conclusions Prepares effective summaries of results and communicates these to wider team Compile and maintain records as required by good laboratory practice Writes clear and technically correct reports with feedback from colleagues Liase with other departments and present technical information to team meetings Have awareness of change control procedures applicable to role Know and apply knowledge of health and safety procedures Responsible for own laboratory notebook and for the accuracy, quality and timeliness of experimental results Ensures that all work complies with the quality system Uses scientific and industry literature to broaden technical and theoretical understanding Highlights improvement opportunities to manager Consistently demonstrates recognised behaviours Basic Qualifications A Levels ( 16 years) STEM subjects desirable but not required Experience of working in a laboratory, scientific or technical environment or other relevant industry Experience of writing technical reports and presenting results Limited technical knowledge Good working knowledge of software packages such as Word, Excel, PowerPoint Randstad Business Support is acting as an Employment Business in relation to this vacancy.
Supporting cutting-edge lithium-ion battery R&D, this contract role offers the chance to join the Advanced Characterisation team of a leading battery organisation. As the Characterisation Scientist, you will carry out routine and advanced analytical testing on battery materials, electrodes, electrolytes and cell components, delivering high-quality data that informs material selection, process development and cell performance across LFP and NMC chemistries. The Characterisation Scientist will be responsible for: Conducting analytical testing using techniques such as BET, PSD, Karl Fischer, titration, TGA/DSC, FTIR, ICP-OES and XRF Preparing powders, electrodes, electrolytes and other samples for analysis Processing and interpreting data, producing clear reports and presenting findings to project teams Operating, maintaining and troubleshooting analytical instrumentation Supporting the development and optimisation of new analytical methods Writing and updating SOPs and maintaining accurate laboratory records Working safely in line with COSHH, risk assessments and EHS procedures The Characterisation Scientist will have: A degree in Chemistry, Materials Science, Physics, Electrochemistry or a related discipline At least two years' experience in an analytical, battery R&D or advanced materials laboratory, or equivalent practical experience Hands-on experience with characterisation techniques such as particle sizing, BET, thermal analysis, spectroscopy and titration Strong data analysis and interpretation skills Experience working to SOPs while maintaining data quality and lab compliance Good written and verbal communication skills Experience with lithium-ion battery materials, LFP or NMC chemistries would be advantageous If you're an analytical scientist looking to apply your lab skills to the next generation of battery technology, we'd be keen to hear from you. Simply apply with your CV and a consultant will be in touch.
Nov 08, 2026
Contractor
Supporting cutting-edge lithium-ion battery R&D, this contract role offers the chance to join the Advanced Characterisation team of a leading battery organisation. As the Characterisation Scientist, you will carry out routine and advanced analytical testing on battery materials, electrodes, electrolytes and cell components, delivering high-quality data that informs material selection, process development and cell performance across LFP and NMC chemistries. The Characterisation Scientist will be responsible for: Conducting analytical testing using techniques such as BET, PSD, Karl Fischer, titration, TGA/DSC, FTIR, ICP-OES and XRF Preparing powders, electrodes, electrolytes and other samples for analysis Processing and interpreting data, producing clear reports and presenting findings to project teams Operating, maintaining and troubleshooting analytical instrumentation Supporting the development and optimisation of new analytical methods Writing and updating SOPs and maintaining accurate laboratory records Working safely in line with COSHH, risk assessments and EHS procedures The Characterisation Scientist will have: A degree in Chemistry, Materials Science, Physics, Electrochemistry or a related discipline At least two years' experience in an analytical, battery R&D or advanced materials laboratory, or equivalent practical experience Hands-on experience with characterisation techniques such as particle sizing, BET, thermal analysis, spectroscopy and titration Strong data analysis and interpretation skills Experience working to SOPs while maintaining data quality and lab compliance Good written and verbal communication skills Experience with lithium-ion battery materials, LFP or NMC chemistries would be advantageous If you're an analytical scientist looking to apply your lab skills to the next generation of battery technology, we'd be keen to hear from you. Simply apply with your CV and a consultant will be in touch.
Associate Scientist 2 - Environmental Monitoring Support Location: Witney, Oxfordshire Salary / Rate: 31,000 per annum Contract Duration: 30 Weeks Department: Quality Assurance / Laboratory Operations About the Role We are seeking a detail-oriented and compliant Associate Scientist to join our team in Witney on a 30-week contract basis. In this role, you will provide vital operational, laboratory, and administrative support for site Environmental Monitoring (EM) programmes. You will play a central role in maintaining a fully compliant Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP) environment through accurate sample collection, rigorous data management, trend analysis, and inspection-ready record keeping. Key Accountabilities & Responsibilities Environmental Monitoring Operations Perform routine environmental monitoring activities, sample collection, labeling, and processing in strict accordance with approved protocols. Support data trending and assist senior team members with investigations into out-of-trend environmental monitoring results. Ensure monitoring equipment, testing materials, and consumables are properly maintained, stocked, and prepared for use. Adhere strictly to GLP and GMP requirements across all monitoring duties. Documentation & Record Management Maintain clear, accurate, and up-to-date batch records, laboratory logbooks, worksheets, and controlled documentation. Review environmental monitoring records for accuracy and completeness to ensure an inspection-ready state. Collate, scan, file, archive, and retrieve paper and electronic laboratory records in line with site retention procedures. Assist with periodic document updates and policy reviews as assigned. Data Management & Reporting Input, verify, and maintain monitoring data within electronic quality management systems and databases. Compile operational data for routine compliance summaries, technical reports, and team presentations. Identify data trends or discrepancies and communicate findings clearly to line management. Quality, Safety & Administrative Support Maintain full compliance with site Quality Systems, standard operating procedures (SOPs), and EHS (Environmental Health & Safety) regulations. Support internal audits, regulatory inspections, and continuous improvement initiatives by preparing required documentation. Provide day-to-day departmental support, including stock inventory control, order raising, and activity scheduling. Key Requirements & Experience Technical Knowledge: Working knowledge of Good Manufacturing Practice (GMP) or Good Laboratory Practice (GLP) principles within a regulated manufacturing or laboratory environment. Systems Proficiency: Strong computer literacy, including MS Office (Excel, Word, PowerPoint) and familiarity with electronic quality or database systems. Data Integrity & Precision: Outstanding attention to detail with strong record-keeping, trend analysis, and document review skills. Organization & Collaboration: Excellent time management skills with the ability to prioritize routine sampling tasks, work effectively in cross-functional teams, and follow strict protocols consistently. Why Apply? This contract position offers a great opportunity to gain hands-on quality and environmental monitoring experience within a highly regulated manufacturing site, developing core skills in GMP compliance, data integrity, and laboratory operations. Randstad Business Support is acting as an Employment Business in relation to this vacancy.
Nov 08, 2026
Seasonal
Associate Scientist 2 - Environmental Monitoring Support Location: Witney, Oxfordshire Salary / Rate: 31,000 per annum Contract Duration: 30 Weeks Department: Quality Assurance / Laboratory Operations About the Role We are seeking a detail-oriented and compliant Associate Scientist to join our team in Witney on a 30-week contract basis. In this role, you will provide vital operational, laboratory, and administrative support for site Environmental Monitoring (EM) programmes. You will play a central role in maintaining a fully compliant Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP) environment through accurate sample collection, rigorous data management, trend analysis, and inspection-ready record keeping. Key Accountabilities & Responsibilities Environmental Monitoring Operations Perform routine environmental monitoring activities, sample collection, labeling, and processing in strict accordance with approved protocols. Support data trending and assist senior team members with investigations into out-of-trend environmental monitoring results. Ensure monitoring equipment, testing materials, and consumables are properly maintained, stocked, and prepared for use. Adhere strictly to GLP and GMP requirements across all monitoring duties. Documentation & Record Management Maintain clear, accurate, and up-to-date batch records, laboratory logbooks, worksheets, and controlled documentation. Review environmental monitoring records for accuracy and completeness to ensure an inspection-ready state. Collate, scan, file, archive, and retrieve paper and electronic laboratory records in line with site retention procedures. Assist with periodic document updates and policy reviews as assigned. Data Management & Reporting Input, verify, and maintain monitoring data within electronic quality management systems and databases. Compile operational data for routine compliance summaries, technical reports, and team presentations. Identify data trends or discrepancies and communicate findings clearly to line management. Quality, Safety & Administrative Support Maintain full compliance with site Quality Systems, standard operating procedures (SOPs), and EHS (Environmental Health & Safety) regulations. Support internal audits, regulatory inspections, and continuous improvement initiatives by preparing required documentation. Provide day-to-day departmental support, including stock inventory control, order raising, and activity scheduling. Key Requirements & Experience Technical Knowledge: Working knowledge of Good Manufacturing Practice (GMP) or Good Laboratory Practice (GLP) principles within a regulated manufacturing or laboratory environment. Systems Proficiency: Strong computer literacy, including MS Office (Excel, Word, PowerPoint) and familiarity with electronic quality or database systems. Data Integrity & Precision: Outstanding attention to detail with strong record-keeping, trend analysis, and document review skills. Organization & Collaboration: Excellent time management skills with the ability to prioritize routine sampling tasks, work effectively in cross-functional teams, and follow strict protocols consistently. Why Apply? This contract position offers a great opportunity to gain hands-on quality and environmental monitoring experience within a highly regulated manufacturing site, developing core skills in GMP compliance, data integrity, and laboratory operations. Randstad Business Support is acting as an Employment Business in relation to this vacancy.
Senior Decision Scientist SME Lending Birmingham based office - Hybrid working - Remote options available if not local I'm currently recruiting for a Senior Decision Scientist to join a growing financial services business, working at the forefront of SME lending and automated credit decisioning . This is a great opportunity for someone who wants to take ownership of the full model lifecycle from identifying the problem and building models through to deployment, monitoring and optimisation - while working closely with Data, Risk and Product teams. What you'll be doing Develop and deploy ML and statistical models across credit risk, affordability and pricing Own models end-to-end, including data, feature engineering, modelling, validation, deployment and monitoring Build model monitoring frameworks and performance dashboards Explore new data sources, challenger models and A/B testing to improve decisioning Turn complex analysis into clear, commercially focused insights Work closely with both technical and senior business stakeholders to influence lending strategy What I'm looking for Strong Machine Learning experience within SME lending or Consumer lending Strong Python and SQL skills Proven experience taking models through the full development lifecycle Background in FinTech, lending or automated decisioning Good understanding of UK credit risk and regulatory requirements Confident communicator who can bridge the gap between Data, Risk and Commercial teams Desirable: Consumer lending experience, model governance/monitoring experience, and a strong commercial mindset with genuine ownership. If you're a Senior Data Scientist, Decision Scientist or Credit Risk Modelling specialist looking for a role where you can have real influence over SME lending strategy , I'd be keen to hear from you. Please apply asap if interested. GleeIT At Gleeson Recruitment Group, we embrace inclusivity and welcome applicants of all backgrounds, experiences, and abilities. We are proud to be a disability confident employer. By applying you will be registered as a candidate with Gleeson Recruitment Limited. Our Privacy Policy is available on our website and explains how we will use your data.
Nov 08, 2026
Full time
Senior Decision Scientist SME Lending Birmingham based office - Hybrid working - Remote options available if not local I'm currently recruiting for a Senior Decision Scientist to join a growing financial services business, working at the forefront of SME lending and automated credit decisioning . This is a great opportunity for someone who wants to take ownership of the full model lifecycle from identifying the problem and building models through to deployment, monitoring and optimisation - while working closely with Data, Risk and Product teams. What you'll be doing Develop and deploy ML and statistical models across credit risk, affordability and pricing Own models end-to-end, including data, feature engineering, modelling, validation, deployment and monitoring Build model monitoring frameworks and performance dashboards Explore new data sources, challenger models and A/B testing to improve decisioning Turn complex analysis into clear, commercially focused insights Work closely with both technical and senior business stakeholders to influence lending strategy What I'm looking for Strong Machine Learning experience within SME lending or Consumer lending Strong Python and SQL skills Proven experience taking models through the full development lifecycle Background in FinTech, lending or automated decisioning Good understanding of UK credit risk and regulatory requirements Confident communicator who can bridge the gap between Data, Risk and Commercial teams Desirable: Consumer lending experience, model governance/monitoring experience, and a strong commercial mindset with genuine ownership. If you're a Senior Data Scientist, Decision Scientist or Credit Risk Modelling specialist looking for a role where you can have real influence over SME lending strategy , I'd be keen to hear from you. Please apply asap if interested. GleeIT At Gleeson Recruitment Group, we embrace inclusivity and welcome applicants of all backgrounds, experiences, and abilities. We are proud to be a disability confident employer. By applying you will be registered as a candidate with Gleeson Recruitment Limited. Our Privacy Policy is available on our website and explains how we will use your data.
We are recruiting for a Senior Scientist to join a growing Toxicology group on behalf of our client, based in Edinburgh. This role involves leading research and development projects in toxicology, with a strong focus on innovative scientific methods. The Senior Scientist will be responsible for designing and overseeing toxicological studies, acting as study director, analysing data, and ensuring project objectives are met in line with regulatory standards. Collaboration with cross-functional teams and providing scientific expertise will be key components of the role. This Senior Scientist role is a senior laboratory-based role requiring expertise in preclinical toxicology, cell-based and biochemical assays, GLP and non-GLP study conduct, and you will play a key role in advancing project goals. Skills & Experience PhD or equivalent experience gained in Analytical Chemistry, Bioanalysis, Pharmaceutical Sciences or related. Proven experience in drug discovery within CRO, pharma or biotech environment. Experience working under GLP regulations and the ability to train others. You will also have experience acting as Study Director on GLP studies. Experience with cell based and biochemical toxicology assays. Joining this organisation offers the opportunity to contribute to innovative toxicology projects and develop your leadership skills within a dynamic environment. The role provides competitive salary packages, professional development opportunities, and the chance to work in a supportive, forward-thinking company committed to scientific excellence.
Nov 08, 2026
Full time
We are recruiting for a Senior Scientist to join a growing Toxicology group on behalf of our client, based in Edinburgh. This role involves leading research and development projects in toxicology, with a strong focus on innovative scientific methods. The Senior Scientist will be responsible for designing and overseeing toxicological studies, acting as study director, analysing data, and ensuring project objectives are met in line with regulatory standards. Collaboration with cross-functional teams and providing scientific expertise will be key components of the role. This Senior Scientist role is a senior laboratory-based role requiring expertise in preclinical toxicology, cell-based and biochemical assays, GLP and non-GLP study conduct, and you will play a key role in advancing project goals. Skills & Experience PhD or equivalent experience gained in Analytical Chemistry, Bioanalysis, Pharmaceutical Sciences or related. Proven experience in drug discovery within CRO, pharma or biotech environment. Experience working under GLP regulations and the ability to train others. You will also have experience acting as Study Director on GLP studies. Experience with cell based and biochemical toxicology assays. Joining this organisation offers the opportunity to contribute to innovative toxicology projects and develop your leadership skills within a dynamic environment. The role provides competitive salary packages, professional development opportunities, and the chance to work in a supportive, forward-thinking company committed to scientific excellence.
Talentmark are recruiting for a Senior R&D Scientist to join a company in the medical devices industry on a contract basis for 12 months. This role is fully site-based in Motherwell. Salary: 24.52 - 26.56 per hour PAYE Senior R&D Scientist Role: Execute complex, high-quality experimental workstreams from concept through to final recommendation and design transfer. Analyse and interpret complex data from multi-factorial experiments. Present project updates and technical findings effectively to stakeholders Apply Design for Manufacture (DFM) philosophy to optimise product formulations and characterisation processes Champion laboratory excellence by creating a working environment that proactively supports compliance, including GLP, GMP, and GDP standards Your Background: Hold a Master's degree in a life science subject. A BSc will be considered if coupled with industry experience. Proven knowledge of diagnostic immunoassay technology and the ability to follow or improve complex experimental protocols. Strong computer literacy and data analysis skills, with a track record of delivering accurate results on time. Excellent communication skills, specifically in writing technical documentation and laboratory records. Experience with particle-based immunoassays, fluorescent detection, whole-blood assays, and working within GMP/GLP/GDP or biohazard environments is preferred. Company: Our client is one of the world's premier innovative biopharmaceutical companies, discovering, developing and providing over 160 different medicines, vaccines and consumer healthcare products to help improve the lives of millions of people in the UK and around the world every year. Apply: For more information, or to apply for this Senior R&D Scientist, please contact Mary Bolt on (phone number removed) or email (url removed). Please quote reference 71382 It is essential that applicants hold entitlement to work in the UK Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
Nov 08, 2026
Contractor
Talentmark are recruiting for a Senior R&D Scientist to join a company in the medical devices industry on a contract basis for 12 months. This role is fully site-based in Motherwell. Salary: 24.52 - 26.56 per hour PAYE Senior R&D Scientist Role: Execute complex, high-quality experimental workstreams from concept through to final recommendation and design transfer. Analyse and interpret complex data from multi-factorial experiments. Present project updates and technical findings effectively to stakeholders Apply Design for Manufacture (DFM) philosophy to optimise product formulations and characterisation processes Champion laboratory excellence by creating a working environment that proactively supports compliance, including GLP, GMP, and GDP standards Your Background: Hold a Master's degree in a life science subject. A BSc will be considered if coupled with industry experience. Proven knowledge of diagnostic immunoassay technology and the ability to follow or improve complex experimental protocols. Strong computer literacy and data analysis skills, with a track record of delivering accurate results on time. Excellent communication skills, specifically in writing technical documentation and laboratory records. Experience with particle-based immunoassays, fluorescent detection, whole-blood assays, and working within GMP/GLP/GDP or biohazard environments is preferred. Company: Our client is one of the world's premier innovative biopharmaceutical companies, discovering, developing and providing over 160 different medicines, vaccines and consumer healthcare products to help improve the lives of millions of people in the UK and around the world every year. Apply: For more information, or to apply for this Senior R&D Scientist, please contact Mary Bolt on (phone number removed) or email (url removed). Please quote reference 71382 It is essential that applicants hold entitlement to work in the UK Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
Senior Analytical Scientist Salary: 40,000 Location: Moreton, UK Start Date: ASAP Contract Type: Permanent About the Role This role supports the Analytical Leadership and Testing (ALT) function within the Regulated Analytical Sciences and Operations (RASO) department. The successful candidate will perform analytical testing of drug substances, intermediates and finished products in a GMP-regulated environment, working closely with laboratory leads and scientific teams. Key Responsibilities Analytical & Laboratory Activities Plan, execute and troubleshoot analytical testing activities in accordance with GMP procedures. Conduct and support analysis using: HPLC Karl Fischer Titration Dissolution Testing Other analytical techniques as required Review, check and approve analytical data and results. Investigate technical issues and support laboratory investigations. Participate in analytical method development, transfer and validation activities. Ensure all analytical records comply with cGMP requirements and ALCOA+ principles. Support internal and external audit readiness activities. Continuous Improvement Identify process improvements and implement solutions. Contribute to Lean initiatives and root cause investigations. Execute tasks in accordance with regulatory and customer-defined standards. Customer & Compliance Build and maintain strong working relationships with customer stakeholders. Ensure all activities align with Synergy's Code of Conduct, Health & Safety, Environmental and Quality standards. Collaborate effectively with laboratory leads, compliance teams, EHS and quality functions. Requirements Qualifications Degree in Chemistry, Analytical Chemistry, Biochemistry or a related scientific discipline. Experience Minimum 3 years' experience working within a GMP laboratory environment. Strong expertise in HPLC and related analytical techniques. Demonstrable experience analysing oral solid dose pharmaceutical products. Experience with dissolution testing and Karl Fischer analysis. Skills & Competencies Strong customer-focused approach. Excellent communication and stakeholder management skills. Ability to work independently and collaboratively within a high-performing team. Strong problem-solving and risk assessment capabilities. Ability to deliver high-quality results whilst maintaining safety and compliance standards. Guidant, Carbon60, Lorien & SRG - The Vertage Group Portfolio are acting as an Employment Business in relation to this vacancy.
Nov 08, 2026
Full time
Senior Analytical Scientist Salary: 40,000 Location: Moreton, UK Start Date: ASAP Contract Type: Permanent About the Role This role supports the Analytical Leadership and Testing (ALT) function within the Regulated Analytical Sciences and Operations (RASO) department. The successful candidate will perform analytical testing of drug substances, intermediates and finished products in a GMP-regulated environment, working closely with laboratory leads and scientific teams. Key Responsibilities Analytical & Laboratory Activities Plan, execute and troubleshoot analytical testing activities in accordance with GMP procedures. Conduct and support analysis using: HPLC Karl Fischer Titration Dissolution Testing Other analytical techniques as required Review, check and approve analytical data and results. Investigate technical issues and support laboratory investigations. Participate in analytical method development, transfer and validation activities. Ensure all analytical records comply with cGMP requirements and ALCOA+ principles. Support internal and external audit readiness activities. Continuous Improvement Identify process improvements and implement solutions. Contribute to Lean initiatives and root cause investigations. Execute tasks in accordance with regulatory and customer-defined standards. Customer & Compliance Build and maintain strong working relationships with customer stakeholders. Ensure all activities align with Synergy's Code of Conduct, Health & Safety, Environmental and Quality standards. Collaborate effectively with laboratory leads, compliance teams, EHS and quality functions. Requirements Qualifications Degree in Chemistry, Analytical Chemistry, Biochemistry or a related scientific discipline. Experience Minimum 3 years' experience working within a GMP laboratory environment. Strong expertise in HPLC and related analytical techniques. Demonstrable experience analysing oral solid dose pharmaceutical products. Experience with dissolution testing and Karl Fischer analysis. Skills & Competencies Strong customer-focused approach. Excellent communication and stakeholder management skills. Ability to work independently and collaboratively within a high-performing team. Strong problem-solving and risk assessment capabilities. Ability to deliver high-quality results whilst maintaining safety and compliance standards. Guidant, Carbon60, Lorien & SRG - The Vertage Group Portfolio are acting as an Employment Business in relation to this vacancy.
Scientist Location : Oak Tree House, Earby, Lancashire, BB18 6JZ Salary : £29,872 - £32,500 DOE Hours : Full-time, 40 hours per week, Monday to Friday Benefits: Annual Bonus: £1,200 based on company and personal performance, Holidays: 25 days plus statutory holidays (option to purchase additional week), Broughton Day: Option for a fixed day off every 2 3 weeks via salary sacrifice, Pension: Auto-enrolment, Life Insurance: 2x death in service and Healthcare: Cash plan Broughton s mission is to improve public health and well-being. As a global contract research organisation, we partner with future-focused organisations and category innovators to bring products to market across the Pharmaceutical, Healthcare, and Lifestyle sectors. Our integrated solutions are delivered by world-leading scientists and regulatory consultants through our contract laboratories. At Broughton, you ll be part of a team that values scientific excellence and innovation. We work on projects that make a real difference to public health, supporting clients in bringing safe, effective products to market. Due to continued growth, we're looking for an industry-experienced Scientist to join our Laboratory Operations team at our Oak Tree House site in Earby. This role would suit someone with at least two years' laboratory experience gained within an industry setting who enjoys hands-on analytical work, takes pride in producing accurate data and thrives in a quality-driven environment. About the Scientist Role: Working as part of a collaborative laboratory team, you'll be responsible for carrying out chemical analysis on a range of client products, ensuring all work is completed in line with agreed quality standards, regulatory requirements and project timelines. You'll be involved in the preparation of samples and reagents, operation of analytical instrumentation and the generation of compliant scientific data that supports client projects across a variety of sectors. As our Scientist you will: Perform analytical testing on client products in accordance with approved methods and study protocols Prepare reagents, samples and standards for analysis Operate and maintain laboratory instrumentation, including: HPLC and LC-MS, GC-FID and GC-MS and CETI-8 Record and review data accurately and in a timely manner Ensure all work complies with GMP, UKAS, ISO standards and internal quality procedures Verify analytical data and complete laboratory documentation to required standards Maintain laboratory housekeeping and equipment standards Investigate out-of-trend results and contribute to non-conformance and deviation investigations Support project delivery through sample coordination, protocol review and client-focused laboratory support Communicate scientific findings clearly through written reports and verbal discussion About You We're looking for somebody who combines strong laboratory experience with a practical, problem-solving mindset. In order to be successful in this role you must have: Minimum of two years' laboratory experience within an industrial, contract testing, pharmaceutical, healthcare or related scientific environment Degree in Chemistry or a related scientific discipline, or equivalent laboratory experience Experience of analytical laboratory techniques Strong attention to detail and data accuracy Good technical problem-solving abilities Competent user of Microsoft Office, particularly Excel Strong communication skills with the ability to work effectively both independently and as part of a team It would be great if you had: Experience of chromatography and mass spectrometry techniques Familiarity with chromatography data systems (CDS) Knowledge of Root Cause Analysis methodologies Experience using statistical or data analysis software Interested If you're an experienced laboratory professional looking to develop your career within a growing scientific organisation, we'd like to hear from you. Apply today to find out more about joining Broughton's team in Earby. Please note: We are unable to provide sponsorship now, or in the future. You must be able to demonstrate your Right to Work in the UK to apply for this role. Without this, your application will be rejected. No agencies please.
Nov 08, 2026
Full time
Scientist Location : Oak Tree House, Earby, Lancashire, BB18 6JZ Salary : £29,872 - £32,500 DOE Hours : Full-time, 40 hours per week, Monday to Friday Benefits: Annual Bonus: £1,200 based on company and personal performance, Holidays: 25 days plus statutory holidays (option to purchase additional week), Broughton Day: Option for a fixed day off every 2 3 weeks via salary sacrifice, Pension: Auto-enrolment, Life Insurance: 2x death in service and Healthcare: Cash plan Broughton s mission is to improve public health and well-being. As a global contract research organisation, we partner with future-focused organisations and category innovators to bring products to market across the Pharmaceutical, Healthcare, and Lifestyle sectors. Our integrated solutions are delivered by world-leading scientists and regulatory consultants through our contract laboratories. At Broughton, you ll be part of a team that values scientific excellence and innovation. We work on projects that make a real difference to public health, supporting clients in bringing safe, effective products to market. Due to continued growth, we're looking for an industry-experienced Scientist to join our Laboratory Operations team at our Oak Tree House site in Earby. This role would suit someone with at least two years' laboratory experience gained within an industry setting who enjoys hands-on analytical work, takes pride in producing accurate data and thrives in a quality-driven environment. About the Scientist Role: Working as part of a collaborative laboratory team, you'll be responsible for carrying out chemical analysis on a range of client products, ensuring all work is completed in line with agreed quality standards, regulatory requirements and project timelines. You'll be involved in the preparation of samples and reagents, operation of analytical instrumentation and the generation of compliant scientific data that supports client projects across a variety of sectors. As our Scientist you will: Perform analytical testing on client products in accordance with approved methods and study protocols Prepare reagents, samples and standards for analysis Operate and maintain laboratory instrumentation, including: HPLC and LC-MS, GC-FID and GC-MS and CETI-8 Record and review data accurately and in a timely manner Ensure all work complies with GMP, UKAS, ISO standards and internal quality procedures Verify analytical data and complete laboratory documentation to required standards Maintain laboratory housekeeping and equipment standards Investigate out-of-trend results and contribute to non-conformance and deviation investigations Support project delivery through sample coordination, protocol review and client-focused laboratory support Communicate scientific findings clearly through written reports and verbal discussion About You We're looking for somebody who combines strong laboratory experience with a practical, problem-solving mindset. In order to be successful in this role you must have: Minimum of two years' laboratory experience within an industrial, contract testing, pharmaceutical, healthcare or related scientific environment Degree in Chemistry or a related scientific discipline, or equivalent laboratory experience Experience of analytical laboratory techniques Strong attention to detail and data accuracy Good technical problem-solving abilities Competent user of Microsoft Office, particularly Excel Strong communication skills with the ability to work effectively both independently and as part of a team It would be great if you had: Experience of chromatography and mass spectrometry techniques Familiarity with chromatography data systems (CDS) Knowledge of Root Cause Analysis methodologies Experience using statistical or data analysis software Interested If you're an experienced laboratory professional looking to develop your career within a growing scientific organisation, we'd like to hear from you. Apply today to find out more about joining Broughton's team in Earby. Please note: We are unable to provide sponsorship now, or in the future. You must be able to demonstrate your Right to Work in the UK to apply for this role. Without this, your application will be rejected. No agencies please.
Contract: 18-month fixed-term contract from signing (running to at least January 2028), with a view to extending or moving to permanent as a second round of programme funding is confirmed Location: Oxford, hybrid preferred, though we'd consider fully remote for the right person. Oxfida (formerly Aioi R&D Lab Oxford) is an AI R&D company based in Oxford, on a mission to harness AI to understand, predict, and manage risk, helping build a safer, more resilient society. We sit at the intersection of academia and industry, working with Oxford's professors and researchers alongside commercial partners, and combining that expertise with real-world risk data at global scale to turn frontier research into AI that actually ships rather than just gets published. Our work spans AI for insurance underwriting and claims, AI risk governance, privacy-preserving technologies for agentic AI, and quantum optimisation, alongside partnership projects on nature and supply chains and the emerging challenges nobody's solved yet. We build AI products and solutions for insurers, businesses, and public-sector organisations worldwide, and run innovative research projects that push these technologies further, helping people make better decisions in an uncertain world. Trusted AI. Built in Oxford. You'd be joining CODAS, our flagship sovereign AI programme, built in partnership with Japanese public and private sector organisations and academic collaborators at Oxford and UCLA. The goal is a privacy-preserving generative and agentic AI ecosystem that protects personal and sensitive data by design, through data residency, anonymisation, secure deployment, and privacy techniques that hold up at both training and inference time. As a Senior Machine Learning Scientist, you'll take technical ownership of research workstreams within CODAS. Rather than just executing a brief, you'll set the experimental direction yourself and push approaches like differential privacy, federated learning, and secure inference beyond what's already out there. Responsibilities Own the technical direction of assigned CODAS research tracks, from framing the problem to validating the results. Design and build ML approaches for privacy-preserving generative AI, including differential privacy, federated learning, secure inference, and related techniques. Turn research into proof-of-concept systems and deployable components that feed directly into programme deliverables. Publish, contributing to papers, technical reports, and conference talks that put Oxfida's work in front of the wider AI community. Mentor other ML scientists and research associates working alongside you on the programme. Work directly with partner organisations to understand real technical constraints, not just theoretical ones. Knowledge, Experience and Qualifications A Master's or PhD in Computer Science, ML, Statistics, Maths, or equivalent experience, plus 5+ years in applied ML/AI research or development. A genuine track record in privacy-preserving ML, generative AI, LLMs, or federated learning, since this isn't a "learn on the job" role. Strong Python engineering skills: ML frameworks, version control, CI/CD, reproducible experiments. Comfort working across the full ML lifecycle, from first prototype to something that can actually be deployed. Experience mentoring others and the communication skills to explain complex trade-offs to non-technical stakeholders. Bonus points: differential privacy or secure computation experience, LLM/agentic AI/frontier AI evaluation work, published research, or experience in regulated industries (insurance, financial services, public sector). Why join us Real technical ownership on a genuinely novel, high-profile programme, not a support role on someone else's research. Direct exposure to Oxford's academic network and CODAS's international partners, not just your immediate team. Work that ships. This isn't research for its own sake; it becomes part of a live sovereign AI ecosystem built with Japanese public and private-sector partners. This is a fixed-term contract tied to CODAS's current funding cycle, but there's a genuine intent to extend and move roles to permanent as a second funding round is confirmed. It isn't a contract designed to end.
Nov 08, 2026
Seasonal
Contract: 18-month fixed-term contract from signing (running to at least January 2028), with a view to extending or moving to permanent as a second round of programme funding is confirmed Location: Oxford, hybrid preferred, though we'd consider fully remote for the right person. Oxfida (formerly Aioi R&D Lab Oxford) is an AI R&D company based in Oxford, on a mission to harness AI to understand, predict, and manage risk, helping build a safer, more resilient society. We sit at the intersection of academia and industry, working with Oxford's professors and researchers alongside commercial partners, and combining that expertise with real-world risk data at global scale to turn frontier research into AI that actually ships rather than just gets published. Our work spans AI for insurance underwriting and claims, AI risk governance, privacy-preserving technologies for agentic AI, and quantum optimisation, alongside partnership projects on nature and supply chains and the emerging challenges nobody's solved yet. We build AI products and solutions for insurers, businesses, and public-sector organisations worldwide, and run innovative research projects that push these technologies further, helping people make better decisions in an uncertain world. Trusted AI. Built in Oxford. You'd be joining CODAS, our flagship sovereign AI programme, built in partnership with Japanese public and private sector organisations and academic collaborators at Oxford and UCLA. The goal is a privacy-preserving generative and agentic AI ecosystem that protects personal and sensitive data by design, through data residency, anonymisation, secure deployment, and privacy techniques that hold up at both training and inference time. As a Senior Machine Learning Scientist, you'll take technical ownership of research workstreams within CODAS. Rather than just executing a brief, you'll set the experimental direction yourself and push approaches like differential privacy, federated learning, and secure inference beyond what's already out there. Responsibilities Own the technical direction of assigned CODAS research tracks, from framing the problem to validating the results. Design and build ML approaches for privacy-preserving generative AI, including differential privacy, federated learning, secure inference, and related techniques. Turn research into proof-of-concept systems and deployable components that feed directly into programme deliverables. Publish, contributing to papers, technical reports, and conference talks that put Oxfida's work in front of the wider AI community. Mentor other ML scientists and research associates working alongside you on the programme. Work directly with partner organisations to understand real technical constraints, not just theoretical ones. Knowledge, Experience and Qualifications A Master's or PhD in Computer Science, ML, Statistics, Maths, or equivalent experience, plus 5+ years in applied ML/AI research or development. A genuine track record in privacy-preserving ML, generative AI, LLMs, or federated learning, since this isn't a "learn on the job" role. Strong Python engineering skills: ML frameworks, version control, CI/CD, reproducible experiments. Comfort working across the full ML lifecycle, from first prototype to something that can actually be deployed. Experience mentoring others and the communication skills to explain complex trade-offs to non-technical stakeholders. Bonus points: differential privacy or secure computation experience, LLM/agentic AI/frontier AI evaluation work, published research, or experience in regulated industries (insurance, financial services, public sector). Why join us Real technical ownership on a genuinely novel, high-profile programme, not a support role on someone else's research. Direct exposure to Oxford's academic network and CODAS's international partners, not just your immediate team. Work that ships. This isn't research for its own sake; it becomes part of a live sovereign AI ecosystem built with Japanese public and private-sector partners. This is a fixed-term contract tied to CODAS's current funding cycle, but there's a genuine intent to extend and move roles to permanent as a second funding round is confirmed. It isn't a contract designed to end.
Scientist - Analytical Testing British Gypsum East Leake At British Gypsum, we're looking for a Scientist to join our Analytical Team within the R&D function. This is an exciting opportunity for a scientist with experience using analytical laboratory techniques to develop their career within a global organisation. Working with samples from across Saint-Gobain's global businesses, you'll carry out analytical testing on gypsum-based products and materials, helping to support product development, innovation and technical projects. As part of one of Saint-Gobain's centres of expertise for gypsum analysis, you'll gain exposure to a wide range of products, technologies and scientific challenges. What you'll be doing Conducting analytical testing on gypsum board and related material samples. Operating analytical instrumentation such as add XRF, XRD GC-MS, HPLC, TGA and/or DSC . Performing routine testing in accordance with established methods and laboratory standards. Preparing samples, conducting experiments and generating high-quality analytical data. Interpreting results and producing clear technical reports. Communicating findings to internal customers, translating technical information into clear and meaningful recommendations. Supporting R&D and innovation projects across British Gypsum and the wider Saint-Gobain Group. Collaborating with colleagues, laboratories and technical teams across the global business. What we're looking for Degree qualified in Chemistry, Materials Science or a related scientific discipline . Experience using analytical laboratory instrumentation such as add XRF, XRD OR GC-MS, HPLC, TGA or DSC , gained through industry, placements, research projects or previous employment. Strong attention to detail and a methodical approach to laboratory work. Ability to analyse and interpret scientific data. Strong written and verbal communication skills. A collaborative approach and willingness to learn and develop. Passion for science, innovation and continuous improvement. Are British Gypsum and Saint-Gobain inclusive employers? Saint-Gobain is a worldwide leader in light and sustainable construction, following our purpose of 'Making the World a Better Home'. We play a part in improving daily life through high-performance solutions. From wherever you are, let your unique personality and our values guide you every day to invent a more sustainable world. We understand that a diverse workplace is not only a more enjoyable place to be, but also facilitates better decision making and innovation. So, whoever you are, and whichever Saint-Gobain business you join, you can be sure of a warm welcome with us. And what about flexibility? At Saint-Gobain, we're always open to new ways of working. Everyone has different needs and commitments. We'll happily discuss any requirements you may have for this role. Whilst we can't promise to meet every request when we're recruiting, we do promise to listen If you match our criteria, we'll be in touch to discuss your experience and learn more about you as a person. We look forward to hearing from you!
Nov 08, 2026
Full time
Scientist - Analytical Testing British Gypsum East Leake At British Gypsum, we're looking for a Scientist to join our Analytical Team within the R&D function. This is an exciting opportunity for a scientist with experience using analytical laboratory techniques to develop their career within a global organisation. Working with samples from across Saint-Gobain's global businesses, you'll carry out analytical testing on gypsum-based products and materials, helping to support product development, innovation and technical projects. As part of one of Saint-Gobain's centres of expertise for gypsum analysis, you'll gain exposure to a wide range of products, technologies and scientific challenges. What you'll be doing Conducting analytical testing on gypsum board and related material samples. Operating analytical instrumentation such as add XRF, XRD GC-MS, HPLC, TGA and/or DSC . Performing routine testing in accordance with established methods and laboratory standards. Preparing samples, conducting experiments and generating high-quality analytical data. Interpreting results and producing clear technical reports. Communicating findings to internal customers, translating technical information into clear and meaningful recommendations. Supporting R&D and innovation projects across British Gypsum and the wider Saint-Gobain Group. Collaborating with colleagues, laboratories and technical teams across the global business. What we're looking for Degree qualified in Chemistry, Materials Science or a related scientific discipline . Experience using analytical laboratory instrumentation such as add XRF, XRD OR GC-MS, HPLC, TGA or DSC , gained through industry, placements, research projects or previous employment. Strong attention to detail and a methodical approach to laboratory work. Ability to analyse and interpret scientific data. Strong written and verbal communication skills. A collaborative approach and willingness to learn and develop. Passion for science, innovation and continuous improvement. Are British Gypsum and Saint-Gobain inclusive employers? Saint-Gobain is a worldwide leader in light and sustainable construction, following our purpose of 'Making the World a Better Home'. We play a part in improving daily life through high-performance solutions. From wherever you are, let your unique personality and our values guide you every day to invent a more sustainable world. We understand that a diverse workplace is not only a more enjoyable place to be, but also facilitates better decision making and innovation. So, whoever you are, and whichever Saint-Gobain business you join, you can be sure of a warm welcome with us. And what about flexibility? At Saint-Gobain, we're always open to new ways of working. Everyone has different needs and commitments. We'll happily discuss any requirements you may have for this role. Whilst we can't promise to meet every request when we're recruiting, we do promise to listen If you match our criteria, we'll be in touch to discuss your experience and learn more about you as a person. We look forward to hearing from you!
Senior Scientist - Analytical Testing East Leake, Nottingham Fulltime, 5 days onsite At British Gypsum, we're looking for a Senior Scientist to join our Analytical Team, helping to deliver high-quality analysis, innovation and technical expertise across our global business. This role sits within our R&D team and offers the opportunity to become a specialist in analytical testing for gypsum-based products. Working with samples from across Saint-Gobain's global businesses, you'll combine hands-on laboratory analysis with method development and technical problem-solving, helping internal customers make informed decisions and drive product innovation. You'll be part of a highly skilled team recognised as a centre of excellence for gypsum analysis across the wider Saint-Gobain Group British Gypsum is part of Saint-Gobain UK & Ireland, a global leader in light and sustainable construction. As the UK's leading manufacturer of interior lining systems, we develop innovative building solutions that help create better living and working environments. This role is full-time and based on-site at our East Leake Innovation Centre. Flexible working arrangements can be discussed. What we're looking for Degree qualified in Chemistry, Materials Science or a related scientific discipline, with relevant industrial experience, or a PhD in a related field. Industrial hands-on experience using analytical instrumentation such as GC-MS, HPLC, TGA and/or DSC. Experience developing, optimising or validating analytical methods within an industrial laboratory environment. Strong data interpretation, report writing and problem-solving skills. Able to communicate complex technical findings clearly to both technical and non-technical stakeholders. What you'll be doing Conduct analytical testing on gypsum board and related material samples using a range of advanced laboratory techniques. Develop and implement new analytical methods from concept through to routine use, supporting product development and technical projects. Generate, interpret and communicate analytical data through technical reports and presentations for internal customers. Support R&D and innovation projects by providing high-quality scientific insight and recommendations. Collaborate with colleagues, research centres and laboratories across Saint-Gobain's global network to share expertise and best practice. Are British Gypsum and Saint-Gobain inclusive employers? Saint-Gobain is a worldwide leader in light and sustainable construction, following our purpose of 'Making the World a Better Home'. We play a part in improving daily life through high-performance solutions. From wherever you are, let your unique personality and our values guide you every day to invent a more sustainable world. We understand that a diverse workplace is not only a more enjoyable place to be, but also facilitates better decision making and innovation. So, whoever you are, and whichever Saint-Gobain business you join, you can be sure of a warm welcome with us. And what about flexibility? At Saint-Gobain, we're always open to new ways of working. Everyone has different needs and commitments. We'll happily discuss any requirements you may have for this role. Whilst we can't promise to meet every request when we're recruiting, we do promise to listen If you match our criteria, we'll be in touch to discuss your experience and learn more about you as a person. We look forward to hearing from you!
Nov 08, 2026
Full time
Senior Scientist - Analytical Testing East Leake, Nottingham Fulltime, 5 days onsite At British Gypsum, we're looking for a Senior Scientist to join our Analytical Team, helping to deliver high-quality analysis, innovation and technical expertise across our global business. This role sits within our R&D team and offers the opportunity to become a specialist in analytical testing for gypsum-based products. Working with samples from across Saint-Gobain's global businesses, you'll combine hands-on laboratory analysis with method development and technical problem-solving, helping internal customers make informed decisions and drive product innovation. You'll be part of a highly skilled team recognised as a centre of excellence for gypsum analysis across the wider Saint-Gobain Group British Gypsum is part of Saint-Gobain UK & Ireland, a global leader in light and sustainable construction. As the UK's leading manufacturer of interior lining systems, we develop innovative building solutions that help create better living and working environments. This role is full-time and based on-site at our East Leake Innovation Centre. Flexible working arrangements can be discussed. What we're looking for Degree qualified in Chemistry, Materials Science or a related scientific discipline, with relevant industrial experience, or a PhD in a related field. Industrial hands-on experience using analytical instrumentation such as GC-MS, HPLC, TGA and/or DSC. Experience developing, optimising or validating analytical methods within an industrial laboratory environment. Strong data interpretation, report writing and problem-solving skills. Able to communicate complex technical findings clearly to both technical and non-technical stakeholders. What you'll be doing Conduct analytical testing on gypsum board and related material samples using a range of advanced laboratory techniques. Develop and implement new analytical methods from concept through to routine use, supporting product development and technical projects. Generate, interpret and communicate analytical data through technical reports and presentations for internal customers. Support R&D and innovation projects by providing high-quality scientific insight and recommendations. Collaborate with colleagues, research centres and laboratories across Saint-Gobain's global network to share expertise and best practice. Are British Gypsum and Saint-Gobain inclusive employers? Saint-Gobain is a worldwide leader in light and sustainable construction, following our purpose of 'Making the World a Better Home'. We play a part in improving daily life through high-performance solutions. From wherever you are, let your unique personality and our values guide you every day to invent a more sustainable world. We understand that a diverse workplace is not only a more enjoyable place to be, but also facilitates better decision making and innovation. So, whoever you are, and whichever Saint-Gobain business you join, you can be sure of a warm welcome with us. And what about flexibility? At Saint-Gobain, we're always open to new ways of working. Everyone has different needs and commitments. We'll happily discuss any requirements you may have for this role. Whilst we can't promise to meet every request when we're recruiting, we do promise to listen If you match our criteria, we'll be in touch to discuss your experience and learn more about you as a person. We look forward to hearing from you!
ROLE OVERVIEW We are currently looking for an Associate Principal Scientist to join our client, a growing scientific organisation based in the Edinburgh area. As the Associate Principal Scientist you will be responsible for designing, delivering and interpreting complex molecular biology studies that support drug discovery and translational research. This laboratory-based scientific leadership role combines hands-on research with technical direction across client programmes. Working with advanced cellular models and molecular biology technologies, you will turn challenging biological questions into robust studies and meaningful findings. As the Associate Principal Scientist, you will also help shape departmental capability, evaluate new technologies and support colleagues in developing their scientific expertise. KEY DUTIES AND RESPONSIBILITIES: Your duties as the Associate Principal Scientist will be varied however the key duties and responsibilities are as follows: 1. Design and deliver complex molecular and cellular biology studies for translational research and drug discovery programmes. You will work with mammalian cell cultures and advanced cellular systems, analysing and interpreting data to produce clear, scientifically sound conclusions. 2. Provide scientific and technical leadership across multiple client projects, coordinating key research activities, troubleshooting experimental challenges and supporting high-quality delivery in line with project objectives and applicable good practice standards. 3. Build effective relationships with clients, scientists and project teams. You will present study findings, explain complex results to scientific and non-scientific audiences, and use your expertise to guide research decisions. 4. Evaluate technologies and develop innovative approaches to challenging biological questions. You will strengthen departmental capability, share best practice, support colleagues and identify opportunities to improve scientific methods and outcomes. ROLE REQUIREMENTS: To be successful in your application to this exciting opportunity as the Associate Principal Scientist we are looking to identify the following on your profile and past history: 1. A doctorate in a relevant scientific discipline, supported by significant postdoctoral, industry or equivalent research experience and a proven track record operating at Senior Scientist level or above. 2. Proven experience in molecular biology, genomics, transcriptomics, cell biology or related disciplines, including hands-on mammalian cell culture and complex cellular systems. Your background will include contract research, biotechnology, pharmaceutical or academic research environments. 3. A working knowledge and practical experience with scientific project leadership, study design, troubleshooting, technology evaluation and delivery of complex research programmes. You will bring confident client communication and presentation skills, a commitment to supporting colleagues and scientific excellence, and the ability to work to applicable good practice standards. Key Words: Senior Scientist / Associate Principal Scientist / Molecular Biology / Translational Biology / Drug Discovery / Mammalian Cell Culture / Genomics / Transcriptomics / Cellular Models / Scientific Project Leadership Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
Nov 07, 2026
Full time
ROLE OVERVIEW We are currently looking for an Associate Principal Scientist to join our client, a growing scientific organisation based in the Edinburgh area. As the Associate Principal Scientist you will be responsible for designing, delivering and interpreting complex molecular biology studies that support drug discovery and translational research. This laboratory-based scientific leadership role combines hands-on research with technical direction across client programmes. Working with advanced cellular models and molecular biology technologies, you will turn challenging biological questions into robust studies and meaningful findings. As the Associate Principal Scientist, you will also help shape departmental capability, evaluate new technologies and support colleagues in developing their scientific expertise. KEY DUTIES AND RESPONSIBILITIES: Your duties as the Associate Principal Scientist will be varied however the key duties and responsibilities are as follows: 1. Design and deliver complex molecular and cellular biology studies for translational research and drug discovery programmes. You will work with mammalian cell cultures and advanced cellular systems, analysing and interpreting data to produce clear, scientifically sound conclusions. 2. Provide scientific and technical leadership across multiple client projects, coordinating key research activities, troubleshooting experimental challenges and supporting high-quality delivery in line with project objectives and applicable good practice standards. 3. Build effective relationships with clients, scientists and project teams. You will present study findings, explain complex results to scientific and non-scientific audiences, and use your expertise to guide research decisions. 4. Evaluate technologies and develop innovative approaches to challenging biological questions. You will strengthen departmental capability, share best practice, support colleagues and identify opportunities to improve scientific methods and outcomes. ROLE REQUIREMENTS: To be successful in your application to this exciting opportunity as the Associate Principal Scientist we are looking to identify the following on your profile and past history: 1. A doctorate in a relevant scientific discipline, supported by significant postdoctoral, industry or equivalent research experience and a proven track record operating at Senior Scientist level or above. 2. Proven experience in molecular biology, genomics, transcriptomics, cell biology or related disciplines, including hands-on mammalian cell culture and complex cellular systems. Your background will include contract research, biotechnology, pharmaceutical or academic research environments. 3. A working knowledge and practical experience with scientific project leadership, study design, troubleshooting, technology evaluation and delivery of complex research programmes. You will bring confident client communication and presentation skills, a commitment to supporting colleagues and scientific excellence, and the ability to work to applicable good practice standards. Key Words: Senior Scientist / Associate Principal Scientist / Molecular Biology / Translational Biology / Drug Discovery / Mammalian Cell Culture / Genomics / Transcriptomics / Cellular Models / Scientific Project Leadership Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
JOB DESCRIPTION JOB TITLE Senior Analytical Scientist LOCATION Sandwich, Kent DEPARTMENT Analytical Control & Development PURPOSE OF ROLE To carry out analytical testing in support of product development, clinical studies and product registration MAIN ACCOUNTABILITIES AND RESPONSIBILITIES To perform this job successfully, an individual must satisfactorily perform the duties below. Reasonable adjustments may be made to enable individuals with disabilities to perform the duties assigned to this role. The job description outlines the main duties and accountabilities in general terms only and is not intended to be prescriptive. Carry out all analytical activities required to deliver new respiratory and other medicinal products to clinical studies and commercialisation Lead the planning of experiments to generate scientific understanding in the development of analytical methods and during formulation development of new products. Process and review data related to product development, stability, and process scale up; interpret results and report experimental outcomes to project development team. Lead the troubleshooting of instrumentation and investigation of aberrant samples results. Maintain laboratory documentation in accordance with the principles of data integrity and good documentation practices. Work with other senior analysts to lead the analytical laboratory operation and identify opportunities for improvements in the working practices and procedures. Oversee the day-to-day work of less experienced analytical laboratory staff. Adherence to all applicable policies and procedures, including those relating to EHS, GMP, GCP, Quality and Compliance, consistent with the role Perform other duties as assigned e.g. laboratory housekeeping, ordering, shipping samples. PERSON SPECIFICATION The requirements for the position are outlined below. A combination of experience and/or education may be taken into consideration. Required: Relevant Bachelor of Science Degree (for example Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Forensics) and substantial practical work experience e.g. through industry or relevant PhD/Post Doctoral roles. Passionate to work in analytical laboratory role. Has a good understanding of basic principles of physical, organic and analytical chemistry and can demonstrate advanced knowledge in specific areas related to their expertise. Highly familiar with calculations used in analytical chemistry and the application of statistics. Has a good understanding and substantial practical experience of modern laboratory techniques including HPLC and demonstrated capability to mentor others. Good understanding of laboratory safety and best practice. Able to work autonomously to deliver multiple tasks, planning own work to consistently achieve high quality results in a timely manner. Able to work collaboratively within a team environment. Good IT skills (including Microsoft Excel, Word, PowerPoint). Effective communication skills, both verbal and written. Guidant, Carbon60, Lorien & SRG - The Vertage Group Portfolio are acting as an Employment Business in relation to this vacancy.
Nov 06, 2026
Full time
JOB DESCRIPTION JOB TITLE Senior Analytical Scientist LOCATION Sandwich, Kent DEPARTMENT Analytical Control & Development PURPOSE OF ROLE To carry out analytical testing in support of product development, clinical studies and product registration MAIN ACCOUNTABILITIES AND RESPONSIBILITIES To perform this job successfully, an individual must satisfactorily perform the duties below. Reasonable adjustments may be made to enable individuals with disabilities to perform the duties assigned to this role. The job description outlines the main duties and accountabilities in general terms only and is not intended to be prescriptive. Carry out all analytical activities required to deliver new respiratory and other medicinal products to clinical studies and commercialisation Lead the planning of experiments to generate scientific understanding in the development of analytical methods and during formulation development of new products. Process and review data related to product development, stability, and process scale up; interpret results and report experimental outcomes to project development team. Lead the troubleshooting of instrumentation and investigation of aberrant samples results. Maintain laboratory documentation in accordance with the principles of data integrity and good documentation practices. Work with other senior analysts to lead the analytical laboratory operation and identify opportunities for improvements in the working practices and procedures. Oversee the day-to-day work of less experienced analytical laboratory staff. Adherence to all applicable policies and procedures, including those relating to EHS, GMP, GCP, Quality and Compliance, consistent with the role Perform other duties as assigned e.g. laboratory housekeeping, ordering, shipping samples. PERSON SPECIFICATION The requirements for the position are outlined below. A combination of experience and/or education may be taken into consideration. Required: Relevant Bachelor of Science Degree (for example Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Forensics) and substantial practical work experience e.g. through industry or relevant PhD/Post Doctoral roles. Passionate to work in analytical laboratory role. Has a good understanding of basic principles of physical, organic and analytical chemistry and can demonstrate advanced knowledge in specific areas related to their expertise. Highly familiar with calculations used in analytical chemistry and the application of statistics. Has a good understanding and substantial practical experience of modern laboratory techniques including HPLC and demonstrated capability to mentor others. Good understanding of laboratory safety and best practice. Able to work autonomously to deliver multiple tasks, planning own work to consistently achieve high quality results in a timely manner. Able to work collaboratively within a team environment. Good IT skills (including Microsoft Excel, Word, PowerPoint). Effective communication skills, both verbal and written. Guidant, Carbon60, Lorien & SRG - The Vertage Group Portfolio are acting as an Employment Business in relation to this vacancy.
Title: Senior AI Scientist Reporting To: Director of Data Science, AI & Research Location: Hybrid, working from home and our office based in West London Salary: £55,000 - £75,000 per annum, dependant on experience We aim to be transparent about remuneration at MHI. As a charitable organisation, salaries for this role are predetermined and not negotiable. Please consider the advertised salary before applying. Hours of Work: 40 hours per week, inclusive of a daily 1 hour paid lunch break. Contract: Permanent Benefits: 25 days annual leave per year, plus public holidays; Company electronic devices; Enhanced salary sacrifice pension scheme; Private health insurance after completion of probation; Eligibility for a Blue Light discount card Closing Date: 20th November 2026. We will be interviewing on a rolling basis and reserve the right to close the job advert early if we receive a high number of applicants, so we encourage applying early. Job Purpose To use AI and data science to understand and improve MHI's services, and to evaluate AI tools so they are used safely, responsibly and only where they add value. Working with the Data Insights team at MHI Impact: Our Data Insights work directly shapes our services and drives our innovation pipeline designed to develop new products and solutions. For example, our recent work, in collaboration with Imperial Global Health Institute, showed an increase in 13s and under using the Shout service, which lead to the development of a proof-of-concept early intervention specifically for 10-13 year olds. Team: You'll join the Data Insights team, working within a multidisciplinary team ( 6-10 people) including data engineers, data scientists, data analysts, research psychologists and a policy lead, with close collaboration with our technical and security teams and links to our clinical and service delivery colleagues. Data and tools: You'll work with a unique dataset: anonymised text from more than 4 million Shout conversations, plus a growing dataset from The Mix's services, including peer support and counselling. All data is held in a secure AWS environment, with Amazon SageMaker for model development and Amazon Bedrock for access to frontier AI models. Responsible data use: Data are securely governed with access on a strict needs basis and research ethics sought where projects extend beyond research purposes for public interest as outlined in the data privacy policy. Wellbeing: As a mental health service that supports those in crisis, we provide insights to colleagues working with sensitive and potentially distressing content. Wellbeing is important to us, and we provide private healthcare and an EAP service that offers mental health support. We also have a number of mental health first aiders that can provide confidential support. Key Responsibilities Conduct research: Investigate open questions about our services and the people who use them, designing studies that produce robust evidence with actionable reports Analyse large-scale text: Apply ML and NLP methods to large volumes of free-text data, such as conversations from our crisis, peer support and counselling services, with careful attention to validity, reliability and bias Prototype and test: Build technical prototypes to test whether AI approaches are viable, and work with colleagues to take promising approaches forward Evaluate AI rigorously: Design and run evaluations of AI models and tools, including prototypes and pilots developed across MHI, validating automated methods against clinical expert judgement and safety testing for high-risk conversations Promote responsible AI: Assess risks, including bias, privacy, safety and potential harm, and help develop appropriate safeguards Shape strategy: Work with the Director of Data Science, AI & Research to develop MHI's AI strategy and research priorities within the Data Insights team Contribute to technical leadership: Help shape technical and methodological standards, support and mentor colleagues, and advise on AI capabilities, limitations, opportunities and risks Collaborate and share knowledge: Work with clinical, service delivery and external partners, communicate complex ideas clearly to non-technical audiences, and contribute to reports, publications and presentations Person Specification Essential A PhD or equivalent experience in a quantitative field, such as computer science, machine learning, statistics, physics, computational neuroscience or quantitative psychology, and a track record of high-quality, well-tested and reproducible technical work you have delivered yourself. Strong Python skills, including proficiency with modern deep learning frameworks (e.g., PyTorch, TensorFlow, JAX, Hugging Face), and working knowledge of SQL for querying data. Hands-on experience applying machine learning and NLP, including large language models, to real-world free text, and turning the results into clear, practical findings. A strong grounding in statistics and research design, and experience designing and running evaluations of AI models or systems, including validation against human judgement. Sound judgement about when AI is and is not the right approach, a preference for the simplest method that solves the problem, and an understanding of responsible AI, including fairness, transparency, privacy and safety. Proactive and self-motivated, with the ability to take initiative, work independently and manage your own priorities, including spotting problems worth solving. Excellent communication and collaboration skills, including explaining technical work to non-specialists and supporting or mentoring colleagues. Ability to handle sensitive mental health data with care, and a commitment to using technology ethically to create positive social impact. Desirable Experience applying AI in mental health, healthcare, or other social and public-interest settings. Knowledge of AI governance, assurance or risk management, including regulation relevant to AI in health. A track record of publications or research reports in machine learning, NLP, AI evaluation or digital mental health. Experience working in AWS or another cloud platform, including running machine learning workloads and using managed AI services. Experience working with external research partners or managing collaborative projects. Experience translating research into practical tools, recommendations or policy. This role is subject to eligibility to work in the UK, plus satisfactory background and reference checks. Unfortunately, we are not able to offer visa sponsorship. We understand that AI is increasingly part of everyday life, and you might choose to use it when putting together your application. While AI can be a helpful tool, we ask that anything you submit reflects your own skills, experiences, and perspective. We value authenticity and integrity, and we want to see what you uniquely bring to our team and why our mission resonates with you personally.
Nov 06, 2026
Full time
Title: Senior AI Scientist Reporting To: Director of Data Science, AI & Research Location: Hybrid, working from home and our office based in West London Salary: £55,000 - £75,000 per annum, dependant on experience We aim to be transparent about remuneration at MHI. As a charitable organisation, salaries for this role are predetermined and not negotiable. Please consider the advertised salary before applying. Hours of Work: 40 hours per week, inclusive of a daily 1 hour paid lunch break. Contract: Permanent Benefits: 25 days annual leave per year, plus public holidays; Company electronic devices; Enhanced salary sacrifice pension scheme; Private health insurance after completion of probation; Eligibility for a Blue Light discount card Closing Date: 20th November 2026. We will be interviewing on a rolling basis and reserve the right to close the job advert early if we receive a high number of applicants, so we encourage applying early. Job Purpose To use AI and data science to understand and improve MHI's services, and to evaluate AI tools so they are used safely, responsibly and only where they add value. Working with the Data Insights team at MHI Impact: Our Data Insights work directly shapes our services and drives our innovation pipeline designed to develop new products and solutions. For example, our recent work, in collaboration with Imperial Global Health Institute, showed an increase in 13s and under using the Shout service, which lead to the development of a proof-of-concept early intervention specifically for 10-13 year olds. Team: You'll join the Data Insights team, working within a multidisciplinary team ( 6-10 people) including data engineers, data scientists, data analysts, research psychologists and a policy lead, with close collaboration with our technical and security teams and links to our clinical and service delivery colleagues. Data and tools: You'll work with a unique dataset: anonymised text from more than 4 million Shout conversations, plus a growing dataset from The Mix's services, including peer support and counselling. All data is held in a secure AWS environment, with Amazon SageMaker for model development and Amazon Bedrock for access to frontier AI models. Responsible data use: Data are securely governed with access on a strict needs basis and research ethics sought where projects extend beyond research purposes for public interest as outlined in the data privacy policy. Wellbeing: As a mental health service that supports those in crisis, we provide insights to colleagues working with sensitive and potentially distressing content. Wellbeing is important to us, and we provide private healthcare and an EAP service that offers mental health support. We also have a number of mental health first aiders that can provide confidential support. Key Responsibilities Conduct research: Investigate open questions about our services and the people who use them, designing studies that produce robust evidence with actionable reports Analyse large-scale text: Apply ML and NLP methods to large volumes of free-text data, such as conversations from our crisis, peer support and counselling services, with careful attention to validity, reliability and bias Prototype and test: Build technical prototypes to test whether AI approaches are viable, and work with colleagues to take promising approaches forward Evaluate AI rigorously: Design and run evaluations of AI models and tools, including prototypes and pilots developed across MHI, validating automated methods against clinical expert judgement and safety testing for high-risk conversations Promote responsible AI: Assess risks, including bias, privacy, safety and potential harm, and help develop appropriate safeguards Shape strategy: Work with the Director of Data Science, AI & Research to develop MHI's AI strategy and research priorities within the Data Insights team Contribute to technical leadership: Help shape technical and methodological standards, support and mentor colleagues, and advise on AI capabilities, limitations, opportunities and risks Collaborate and share knowledge: Work with clinical, service delivery and external partners, communicate complex ideas clearly to non-technical audiences, and contribute to reports, publications and presentations Person Specification Essential A PhD or equivalent experience in a quantitative field, such as computer science, machine learning, statistics, physics, computational neuroscience or quantitative psychology, and a track record of high-quality, well-tested and reproducible technical work you have delivered yourself. Strong Python skills, including proficiency with modern deep learning frameworks (e.g., PyTorch, TensorFlow, JAX, Hugging Face), and working knowledge of SQL for querying data. Hands-on experience applying machine learning and NLP, including large language models, to real-world free text, and turning the results into clear, practical findings. A strong grounding in statistics and research design, and experience designing and running evaluations of AI models or systems, including validation against human judgement. Sound judgement about when AI is and is not the right approach, a preference for the simplest method that solves the problem, and an understanding of responsible AI, including fairness, transparency, privacy and safety. Proactive and self-motivated, with the ability to take initiative, work independently and manage your own priorities, including spotting problems worth solving. Excellent communication and collaboration skills, including explaining technical work to non-specialists and supporting or mentoring colleagues. Ability to handle sensitive mental health data with care, and a commitment to using technology ethically to create positive social impact. Desirable Experience applying AI in mental health, healthcare, or other social and public-interest settings. Knowledge of AI governance, assurance or risk management, including regulation relevant to AI in health. A track record of publications or research reports in machine learning, NLP, AI evaluation or digital mental health. Experience working in AWS or another cloud platform, including running machine learning workloads and using managed AI services. Experience working with external research partners or managing collaborative projects. Experience translating research into practical tools, recommendations or policy. This role is subject to eligibility to work in the UK, plus satisfactory background and reference checks. Unfortunately, we are not able to offer visa sponsorship. We understand that AI is increasingly part of everyday life, and you might choose to use it when putting together your application. While AI can be a helpful tool, we ask that anything you submit reflects your own skills, experiences, and perspective. We value authenticity and integrity, and we want to see what you uniquely bring to our team and why our mission resonates with you personally.