QC Laboratory Manager We are seeking a Laboratory Manager to lead our clients' QC function and support the delivery of high quality analytical services to manufacturing and development teams. The role will play a key part in strengthening laboratory performance, improving efficiency, and driving continuous improvement across the business. Hours of work would be 08.00 - 16.30 Monday to Friday. Responsibilities include: Leading and developing a team of QC analysts and technicians Managing the Laboratory day to day Supporting investigations and troubleshooting Driving improvements in the Laboratory Acting as the interface between QC, manufacturing, and development teams Candidate Profile: Strong background in Analytical / QC Labs Experience in leading or supervising teams Proven ability to drive performance and continuous improvement Strong communication and cross functional working skills Due to the high volume of candidates responding to our adverts unfortunately we are not always able to provide individual feedback. If you don't hear from us within the next ten days, please assume you have been unsuccessful on this occasion. We will however keep your details on file and you may be contacted about other opportunities in the future.
Apr 01, 2026
Full time
QC Laboratory Manager We are seeking a Laboratory Manager to lead our clients' QC function and support the delivery of high quality analytical services to manufacturing and development teams. The role will play a key part in strengthening laboratory performance, improving efficiency, and driving continuous improvement across the business. Hours of work would be 08.00 - 16.30 Monday to Friday. Responsibilities include: Leading and developing a team of QC analysts and technicians Managing the Laboratory day to day Supporting investigations and troubleshooting Driving improvements in the Laboratory Acting as the interface between QC, manufacturing, and development teams Candidate Profile: Strong background in Analytical / QC Labs Experience in leading or supervising teams Proven ability to drive performance and continuous improvement Strong communication and cross functional working skills Due to the high volume of candidates responding to our adverts unfortunately we are not always able to provide individual feedback. If you don't hear from us within the next ten days, please assume you have been unsuccessful on this occasion. We will however keep your details on file and you may be contacted about other opportunities in the future.
Key Responsibilities: • Provision of nursing veterinary care during routine and non-routine veterinary rounds and surgery. • Provision of nursing support to the pet population without direct support from the Veterinary Surgeon through nurse clinics and health screening. • Work closely with the Named Veterinary Surgeons (NVS) and Operations Activity Manager (OAM) to ensure the effective co-ordination, delivery and continuous improvement of the animal healthcare programme. • Development of training material and training of site personnel in veterinary care. This includes but is not limited to training of unit teams in pet health assessments, treatment administration and tasks related to breeding. • Manage and be accountable for the veterinary suites, laboratory area and consult rooms. Ensuring that they are appropriately equipped, stocked and fit for purpose, operating at maximum efficiency and effectiveness. • Work cross functionally with Veterinary Services, Unit Operations, Behaviour and Training and Research teams to ensure trials are delivered safely and effectively. • Drive continuous improvement, share best practice, actively participate in team meetings and initiatives. Context/ Scope: The Waltham animal population comprises approximately 200 dogs and 200 cats. The job holder reports to the Veterinary Operations lead and will work within a team of four veterinary nurses and four full time veterinary surgeons. The job holder is expected to communicate effectively within this team environment, as well as within the wider Veterinary Operations and other Waltham teams: • A Standard working week 37.5 h/week Monday to Friday. The working day is 7.5hrs, and the role holder must be able to be flexible with regard to start and finish times within the hours of 8AM to 6PM. • Participation in the evening and weekend on-call rota (approx. 1 in 4) is required. • The job holder is expected to keep the functional technical knowledge necessary to be successful in the role up to date and must complete their annual RCVS CPD requirement, which will be supported by the business. Qualifications and Experience: • Registered Veterinary Nurse (RCVS) - Bachelor (Bsc) or Foundation (FdSc) degree in veterinary nursing (Essential). • Completion of continuous professional development (CPD) courses in anesthesia or animal behaviour and welfare (Desirable). • GCSE's in English, Maths and Science at grade C/4 or above. • Experience of 5 years in small-animal veterinary practice. Ability to demonstrate triage skills and experience working on-call. • Experience in anaesthesia and sedation techniques. • Companion animal welfare, behaviour and low stress handling experience. • Proven effectiveness in cross functional teams and collaborative environments. Being able to demonstrate teamwork Is essential. • Strong attention to detail and data quality, must be able to follow SOP's and maintain accurate records.
Apr 01, 2026
Contractor
Key Responsibilities: • Provision of nursing veterinary care during routine and non-routine veterinary rounds and surgery. • Provision of nursing support to the pet population without direct support from the Veterinary Surgeon through nurse clinics and health screening. • Work closely with the Named Veterinary Surgeons (NVS) and Operations Activity Manager (OAM) to ensure the effective co-ordination, delivery and continuous improvement of the animal healthcare programme. • Development of training material and training of site personnel in veterinary care. This includes but is not limited to training of unit teams in pet health assessments, treatment administration and tasks related to breeding. • Manage and be accountable for the veterinary suites, laboratory area and consult rooms. Ensuring that they are appropriately equipped, stocked and fit for purpose, operating at maximum efficiency and effectiveness. • Work cross functionally with Veterinary Services, Unit Operations, Behaviour and Training and Research teams to ensure trials are delivered safely and effectively. • Drive continuous improvement, share best practice, actively participate in team meetings and initiatives. Context/ Scope: The Waltham animal population comprises approximately 200 dogs and 200 cats. The job holder reports to the Veterinary Operations lead and will work within a team of four veterinary nurses and four full time veterinary surgeons. The job holder is expected to communicate effectively within this team environment, as well as within the wider Veterinary Operations and other Waltham teams: • A Standard working week 37.5 h/week Monday to Friday. The working day is 7.5hrs, and the role holder must be able to be flexible with regard to start and finish times within the hours of 8AM to 6PM. • Participation in the evening and weekend on-call rota (approx. 1 in 4) is required. • The job holder is expected to keep the functional technical knowledge necessary to be successful in the role up to date and must complete their annual RCVS CPD requirement, which will be supported by the business. Qualifications and Experience: • Registered Veterinary Nurse (RCVS) - Bachelor (Bsc) or Foundation (FdSc) degree in veterinary nursing (Essential). • Completion of continuous professional development (CPD) courses in anesthesia or animal behaviour and welfare (Desirable). • GCSE's in English, Maths and Science at grade C/4 or above. • Experience of 5 years in small-animal veterinary practice. Ability to demonstrate triage skills and experience working on-call. • Experience in anaesthesia and sedation techniques. • Companion animal welfare, behaviour and low stress handling experience. • Proven effectiveness in cross functional teams and collaborative environments. Being able to demonstrate teamwork Is essential. • Strong attention to detail and data quality, must be able to follow SOP's and maintain accurate records.
Randox Laboratories
Newcastle Upon Tyne, Tyne And Wear
Phlebotomist - Newcastle - (Job Ref: 26/PBNE) Randox Health continues to be at the forefront of clinical diagnostics, dedicated to improving health worldwide with our disruptive technology and innovative diagnostic solutions. Our staff are at the heart of everything we do and achieve. We have an exciting new career opportunity for a Phlebotomist within our clinic in the John Lewis store in Eldon Square in Newcastle. What does the Randox Health team do? At Randox Health we encourage individuals to adopt a personalised, preventative approach to their health and well-being, ultimately helping them to live healthier for longer. Using Randox revolutionary technology we measure hundreds of health biomarkers, generating unrivalled data that when combined with our complex algorithms can predict future health concerns and identify early signs of illness even before symptoms arise. This empowers individuals to act sooner to prevent or delay disease onset - moving from a model of sickness management to true preventative healthcare. Our unique biomarker tracking service allows you to establish a health baseline from which you can track and monitor improvements over time. Location: Eldon Square, Percy St, Newcastle upon Tyne NE1 7RR. Contract Offered: Full-time, Permanent Working Hours / Shifts: 40 hours per week, across 5 days, within the clinic opening hours of 8.45am to 6.20pm including some weekends and evenings. For this position, as you may be in contact with live blood samples, you must be vaccinated against Hepatitis B or be able to get it following a successful interview stage. In line with Care Quality Commission guidelines, the successful candidate will be required to undergo an enhanced Disclosure and Barring Service check. Right to Work Requirement Please note that this role requires candidates to have the legal right to work in the UK for a minimum of 12 months from the application date. This is to ensure completion of our 9-month probationary period and for any potential sponsorship decisions to be considered. Unfortunately, we are unable to offer visa sponsorship at the point of hire. What does the Phlebotomist role involve? This role is responsible for ensuring customers have an excellent experience from the moment they enter our clinic, taking blood samples from both private and corporate clients. This is a varied role that may also include the following responsibilities: Conduct comprehensive client appointments, including blood and urine sample collection, personal health measurements, and data entry into our Patient Information Systems (PIS). Demonstrate sensitive communication to ensure client understanding and consent. Maintain accurate records in PIS, uploading all relevant documentation. Represent the company professionally at offsite events and appointments. Engage in upselling and cross-selling at our private health clinic. Proactively drive sales and exceed targets. Complete company forms, specimen labelling, and laboratory test order forms accurately. Demonstrate high IT literacy in order to manager various software systems and daily tasks. Essential criteria: Previous Phlebotomy experience and certificate or equivalent training. Confident using IT programmes. Flexibility with working hours, as required by the business inclusive of evenings and weekends. Flexibility to work from offsite locations at least once per month. Currently have the right to work in the UK without visa sponsorship. Strong communication skills. Desirable: Experience in a private healthcare setting. Exeperience in customer service. 2 years experience in Phlebotomy. Sales / Retail experience. Valid UK driving licence. How do I apply? Click Apply on the site you are seeing this advert on they will submit your CV to Randox for review. This advert may be open for as long as 30 days although we may close the advert early if we receive sufficient applicants to fill the roles. About Randox Health: For almost 40 years Randox has been at the forefront of clinical diagnostics, dedicated to improving health worldwide with our disruptive technology and innovative diagnostic solutions. This experience and expertise powers each of our state-of-the-art Randox Health clinics, based in over 40 locations across the UK and Ireland. A mobile service enabling certified Randox Health staff to visit clients at their convenience is also available. In early 2020, Randox were one of the first to respond to the coronavirus pandemic, developing a pioneering diagnostic test for COVID-19 in just a few weeks. Our rapid COVID-19 testing service is trusted and was used by a variety of private companies and individuals, including the sports industry and in the UK Government's National COVID-19 Testing Programme.
Apr 01, 2026
Full time
Phlebotomist - Newcastle - (Job Ref: 26/PBNE) Randox Health continues to be at the forefront of clinical diagnostics, dedicated to improving health worldwide with our disruptive technology and innovative diagnostic solutions. Our staff are at the heart of everything we do and achieve. We have an exciting new career opportunity for a Phlebotomist within our clinic in the John Lewis store in Eldon Square in Newcastle. What does the Randox Health team do? At Randox Health we encourage individuals to adopt a personalised, preventative approach to their health and well-being, ultimately helping them to live healthier for longer. Using Randox revolutionary technology we measure hundreds of health biomarkers, generating unrivalled data that when combined with our complex algorithms can predict future health concerns and identify early signs of illness even before symptoms arise. This empowers individuals to act sooner to prevent or delay disease onset - moving from a model of sickness management to true preventative healthcare. Our unique biomarker tracking service allows you to establish a health baseline from which you can track and monitor improvements over time. Location: Eldon Square, Percy St, Newcastle upon Tyne NE1 7RR. Contract Offered: Full-time, Permanent Working Hours / Shifts: 40 hours per week, across 5 days, within the clinic opening hours of 8.45am to 6.20pm including some weekends and evenings. For this position, as you may be in contact with live blood samples, you must be vaccinated against Hepatitis B or be able to get it following a successful interview stage. In line with Care Quality Commission guidelines, the successful candidate will be required to undergo an enhanced Disclosure and Barring Service check. Right to Work Requirement Please note that this role requires candidates to have the legal right to work in the UK for a minimum of 12 months from the application date. This is to ensure completion of our 9-month probationary period and for any potential sponsorship decisions to be considered. Unfortunately, we are unable to offer visa sponsorship at the point of hire. What does the Phlebotomist role involve? This role is responsible for ensuring customers have an excellent experience from the moment they enter our clinic, taking blood samples from both private and corporate clients. This is a varied role that may also include the following responsibilities: Conduct comprehensive client appointments, including blood and urine sample collection, personal health measurements, and data entry into our Patient Information Systems (PIS). Demonstrate sensitive communication to ensure client understanding and consent. Maintain accurate records in PIS, uploading all relevant documentation. Represent the company professionally at offsite events and appointments. Engage in upselling and cross-selling at our private health clinic. Proactively drive sales and exceed targets. Complete company forms, specimen labelling, and laboratory test order forms accurately. Demonstrate high IT literacy in order to manager various software systems and daily tasks. Essential criteria: Previous Phlebotomy experience and certificate or equivalent training. Confident using IT programmes. Flexibility with working hours, as required by the business inclusive of evenings and weekends. Flexibility to work from offsite locations at least once per month. Currently have the right to work in the UK without visa sponsorship. Strong communication skills. Desirable: Experience in a private healthcare setting. Exeperience in customer service. 2 years experience in Phlebotomy. Sales / Retail experience. Valid UK driving licence. How do I apply? Click Apply on the site you are seeing this advert on they will submit your CV to Randox for review. This advert may be open for as long as 30 days although we may close the advert early if we receive sufficient applicants to fill the roles. About Randox Health: For almost 40 years Randox has been at the forefront of clinical diagnostics, dedicated to improving health worldwide with our disruptive technology and innovative diagnostic solutions. This experience and expertise powers each of our state-of-the-art Randox Health clinics, based in over 40 locations across the UK and Ireland. A mobile service enabling certified Randox Health staff to visit clients at their convenience is also available. In early 2020, Randox were one of the first to respond to the coronavirus pandemic, developing a pioneering diagnostic test for COVID-19 in just a few weeks. Our rapid COVID-19 testing service is trusted and was used by a variety of private companies and individuals, including the sports industry and in the UK Government's National COVID-19 Testing Programme.
Senior RF Engineer Edinburgh 12-month contract Paying up to 80p/h (Inside IR35) The Opportunity Our client is looking for Senior RF Engineers to join a leading defence technology organisation developing cutting-edge radar systems for modern fighter aircraft, as well as advanced maritime and airborne surveillance platforms. Key Responsibilities As an RF/Microwave Engineer, you will: Support the full hardware lifecycle from system concept through design, prototyping, test, verification, integration and production support. Develop high-quality RF PCB and module designs using modern microwave technologies. Create test prototypes to validate and verify designs. Carry out detailed design activities from requirements capture through to verification. Produce and maintain clear technical documentation and reports under configuration management. Prepare manufacturing data packs and support subcontractors and manufacturing teams. Work closely with systems, electronics and test engineers to resolve complex integration challenges. Participate in and support design reviews and lifecycle management activities. Essential Skills & Experience A degree in Electrical & Electronic Engineering (BSc, BEng, MEng, MSc, PhD, EngD) is preferred, although closely related disciplines such as Physics will also be considered. Microwave PCB materials and RF design techniques RF/Microwave subsystem design Microwave design tools (e.g. AWR, ADS, SystemVue, MATLAB) EM simulation techniques (2D/3D), e.g. CST GaAs/GaN MMIC design and applications RF synthesiser design (DDS and PLL technologies) RF downconverter and digitiser design Passive microwave structure design Non-linear circuit simulation PCB schematic capture tools (e.g. Mentor) RF laboratory measurements (signal generators, spectrum analysers, vector network analysers) Requirements capture and technical report writing Design for manufacture and cost Disclaimer: This vacancy is being advertised by either Advanced Resource Managers Limited, Advanced Resource Managers IT Limited or Advanced Resource Managers Engineering Limited ("ARM"). ARM is a specialist talent acquisition and management consultancy. We provide technical contingency recruitment and a portfolio of more complex resource solutions. Our specialist recruitment divisions cover the entire technical arena, including some of the most economically and strategically important industries in the UK and the world today. We will never send your CV without your permission. Where the role is marked as Outside IR35 in the advertisement this is subject to receipt of a final Status Determination Statement from the end Client and may be subject to change.
Apr 01, 2026
Contractor
Senior RF Engineer Edinburgh 12-month contract Paying up to 80p/h (Inside IR35) The Opportunity Our client is looking for Senior RF Engineers to join a leading defence technology organisation developing cutting-edge radar systems for modern fighter aircraft, as well as advanced maritime and airborne surveillance platforms. Key Responsibilities As an RF/Microwave Engineer, you will: Support the full hardware lifecycle from system concept through design, prototyping, test, verification, integration and production support. Develop high-quality RF PCB and module designs using modern microwave technologies. Create test prototypes to validate and verify designs. Carry out detailed design activities from requirements capture through to verification. Produce and maintain clear technical documentation and reports under configuration management. Prepare manufacturing data packs and support subcontractors and manufacturing teams. Work closely with systems, electronics and test engineers to resolve complex integration challenges. Participate in and support design reviews and lifecycle management activities. Essential Skills & Experience A degree in Electrical & Electronic Engineering (BSc, BEng, MEng, MSc, PhD, EngD) is preferred, although closely related disciplines such as Physics will also be considered. Microwave PCB materials and RF design techniques RF/Microwave subsystem design Microwave design tools (e.g. AWR, ADS, SystemVue, MATLAB) EM simulation techniques (2D/3D), e.g. CST GaAs/GaN MMIC design and applications RF synthesiser design (DDS and PLL technologies) RF downconverter and digitiser design Passive microwave structure design Non-linear circuit simulation PCB schematic capture tools (e.g. Mentor) RF laboratory measurements (signal generators, spectrum analysers, vector network analysers) Requirements capture and technical report writing Design for manufacture and cost Disclaimer: This vacancy is being advertised by either Advanced Resource Managers Limited, Advanced Resource Managers IT Limited or Advanced Resource Managers Engineering Limited ("ARM"). ARM is a specialist talent acquisition and management consultancy. We provide technical contingency recruitment and a portfolio of more complex resource solutions. Our specialist recruitment divisions cover the entire technical arena, including some of the most economically and strategically important industries in the UK and the world today. We will never send your CV without your permission. Where the role is marked as Outside IR35 in the advertisement this is subject to receipt of a final Status Determination Statement from the end Client and may be subject to change.
Kendall Poole Consulting Ltd
Stafford, Staffordshire
TECHNICAL DIRECTOR Manufacturing Sector Location: Staffordshire Salary: Six Figure Executive Package Kendall Poole Consulting are proud to represent a market leading iron casting and machining group supplying both the domestic and export markets. Our client undertakes the design, including virtual analysis, of cast iron, produce rapid prototypes and pre-series castings using full production processes, as well as producing serial quantities of fully machined ductile iron castings and sub-assemblies. They combine state of the art laboratory facilities, with world class technical and operational expertise, and a vacancy has arisen for a Technical Director to lead a team of Managers, Lab Technicians and Method Engineers. The Role: Reporting to the MD, the Technical Director is responsible for leading the technical function and devising the strategy to improve processes which include greensand, cold-box and shell core making, electric melting (99% ductile iron), ABB robots, Koyama grinding, internal heat treatment, crack detection and 3D scanning. Whilst making improvements across the function, implementing new processes and providing an exceptional level of customer service, you will ensure that Technical/Laboratory/Engineering resources and objectives are aligned with strategic plan. To drive innovation in Metallurgy, you will evolve the NPI process, manage and improve deployment of resources: focus on people and training, budgets and assets to comply with cost and financial targets. Customer facing and involves building strong relationships with international manufacturers to deliver on time. Review and advise customers on material standards, presenting any irregularities in line with SOP and provide solutions for heat treatment, chemistry requirements, testing frequency etc. Lead on reviewing customer supplied drawings and advise of any irregularities for hardness test methods, mechanical testing from casting, post processing operations, magnetic resonance etc. Project based work such as commissioning automated inoculation systems, yield improvements through metal control and compositional changes etc. The Person: As part of the SLT operating within an open management culture, you will have the remit to influence the technical strategy of this highly successful and profitable business. A high achiever academically, a qualified Engineer or Scientist with deep knowledge of advanced material science, material forming, metallurgy, metallurgical processes or equivalent. Skilled in developing NPI processes, material innovation and testing, R&D, failure and stress analysis, you will be in a lead technical role, operating within the manufacturing sector, ideally within the foundry industry. Knowledge of cast processes such as greensand, cold-box and shell core making would be beneficial. Extensive customer exposure to an international customer base and/or prestigious OEMs. A focused and collaborative leader, with integrity is sought, people focussed with a team mentality and well-honed leadership skills, who can work closely with a dynamic Board. Visible leader with the ability to motivate a team to achieve higher levels of performance. Exceptional interpersonal and communication skills, you will be able to see the bigger picture yet be analytical, data driven, results focused whilst displaying gravitas, energy and positivity. In return they offer a six-figure package, which includes salary, bonus, car allowance, healthcare for family, DIS, pension and holidays, which accrue on service.
Apr 01, 2026
Full time
TECHNICAL DIRECTOR Manufacturing Sector Location: Staffordshire Salary: Six Figure Executive Package Kendall Poole Consulting are proud to represent a market leading iron casting and machining group supplying both the domestic and export markets. Our client undertakes the design, including virtual analysis, of cast iron, produce rapid prototypes and pre-series castings using full production processes, as well as producing serial quantities of fully machined ductile iron castings and sub-assemblies. They combine state of the art laboratory facilities, with world class technical and operational expertise, and a vacancy has arisen for a Technical Director to lead a team of Managers, Lab Technicians and Method Engineers. The Role: Reporting to the MD, the Technical Director is responsible for leading the technical function and devising the strategy to improve processes which include greensand, cold-box and shell core making, electric melting (99% ductile iron), ABB robots, Koyama grinding, internal heat treatment, crack detection and 3D scanning. Whilst making improvements across the function, implementing new processes and providing an exceptional level of customer service, you will ensure that Technical/Laboratory/Engineering resources and objectives are aligned with strategic plan. To drive innovation in Metallurgy, you will evolve the NPI process, manage and improve deployment of resources: focus on people and training, budgets and assets to comply with cost and financial targets. Customer facing and involves building strong relationships with international manufacturers to deliver on time. Review and advise customers on material standards, presenting any irregularities in line with SOP and provide solutions for heat treatment, chemistry requirements, testing frequency etc. Lead on reviewing customer supplied drawings and advise of any irregularities for hardness test methods, mechanical testing from casting, post processing operations, magnetic resonance etc. Project based work such as commissioning automated inoculation systems, yield improvements through metal control and compositional changes etc. The Person: As part of the SLT operating within an open management culture, you will have the remit to influence the technical strategy of this highly successful and profitable business. A high achiever academically, a qualified Engineer or Scientist with deep knowledge of advanced material science, material forming, metallurgy, metallurgical processes or equivalent. Skilled in developing NPI processes, material innovation and testing, R&D, failure and stress analysis, you will be in a lead technical role, operating within the manufacturing sector, ideally within the foundry industry. Knowledge of cast processes such as greensand, cold-box and shell core making would be beneficial. Extensive customer exposure to an international customer base and/or prestigious OEMs. A focused and collaborative leader, with integrity is sought, people focussed with a team mentality and well-honed leadership skills, who can work closely with a dynamic Board. Visible leader with the ability to motivate a team to achieve higher levels of performance. Exceptional interpersonal and communication skills, you will be able to see the bigger picture yet be analytical, data driven, results focused whilst displaying gravitas, energy and positivity. In return they offer a six-figure package, which includes salary, bonus, car allowance, healthcare for family, DIS, pension and holidays, which accrue on service.
Pesticide Compliance Manager We are seeking a knowledgeable and detail-oriented professional to lead pesticide compliance activity across a diverse fresh produce supply network. This role is central to maintaining regulatory adherence, customer policy alignment, and environmental due diligence across multiple regions. Pesticide Compliance Manager Key Responsibilities Take full ownership of pesticide compliance processes across suppliers and product categories Manage concession and derogation submissions, ensuring accurate data collation and timely approval Review spray records, authorisations and laboratory residue analysis to verify compliance Maintain and update pesticide risk assessments, reporting emerging risks to stakeholders Lead investigations into non-conformances, documenting root cause analysis and corrective actions Engage suppliers to implement mitigation plans and long-term preventative measures Support risk-based site assessments in collaboration with auditing colleagues Conduct recall and traceability exercises to validate supplier control systems Pesticide Compliance Manager Key Skills and Experience Degree educated in a scientific discipline Demonstrable knowledge of pesticide legislation and residue compliance Advanced capability in Microsoft Excel and data analysis tools Experience interpreting technical documentation and regulatory standards Strong organisational skills with the ability to manage multiple priorities Confident communicator with the ability to influence cross-functional stakeholders This is a full-time position based in Kent. Applicants must have the legal right to work in the United Kingdom, and evidence of this right will be required prior to interview.
Apr 01, 2026
Full time
Pesticide Compliance Manager We are seeking a knowledgeable and detail-oriented professional to lead pesticide compliance activity across a diverse fresh produce supply network. This role is central to maintaining regulatory adherence, customer policy alignment, and environmental due diligence across multiple regions. Pesticide Compliance Manager Key Responsibilities Take full ownership of pesticide compliance processes across suppliers and product categories Manage concession and derogation submissions, ensuring accurate data collation and timely approval Review spray records, authorisations and laboratory residue analysis to verify compliance Maintain and update pesticide risk assessments, reporting emerging risks to stakeholders Lead investigations into non-conformances, documenting root cause analysis and corrective actions Engage suppliers to implement mitigation plans and long-term preventative measures Support risk-based site assessments in collaboration with auditing colleagues Conduct recall and traceability exercises to validate supplier control systems Pesticide Compliance Manager Key Skills and Experience Degree educated in a scientific discipline Demonstrable knowledge of pesticide legislation and residue compliance Advanced capability in Microsoft Excel and data analysis tools Experience interpreting technical documentation and regulatory standards Strong organisational skills with the ability to manage multiple priorities Confident communicator with the ability to influence cross-functional stakeholders This is a full-time position based in Kent. Applicants must have the legal right to work in the United Kingdom, and evidence of this right will be required prior to interview.
QA Laboratory Technician Magor 22.35- 44.70 per hour 4 on 4 off (2 Days, 2 Nights) Temporary Long-Term Introduction Acorn by Synergie is recruiting a QA Laboratory Technician to join a global brewing company based in Magor. This is a temporary long-term opportunity offering a structured shift pattern, competitive pay rates and overtime opportunities within a fast-paced production environment. Reporting to the QA First Line Manager, you will be responsible for carrying out Quality Assurance analyses across the brewery, ensuring QA policies and procedures are adhered to at all times. You will communicate quality issues to relevant managers and accurately record and report QA data using various software systems. Please note this job description is not exhaustive, and flexibility will be required to undertake reasonable additional duties within your capabilities. Key Duties Deploy existing and new operating practices across the department. Contribute to preventing quality defects reaching customers. Provide QA support across site, responding to quality issues. Monitor performance to ensure specifications, systems and procedures meet product quality and food/feed safety requirements. Undertake routine analysis of samples. Perform calibration and maintenance on laboratory instrumentation. Assist with basic microbiology tasks. Complete required data entry, interpret results and present data at production meetings. Manage hold beer inspections and prepare the taste room for tasting sessions. Train and audit Brewing and Operations staff on QA processes. Participate in root cause analysis and drive process improvements. Contribute to cost optimisation initiatives and departmental projects. Promote safe working practices and ensure compliance with Food Safety, Integrity, Legality and Quality Standards. Maintain departmental SOPs and ensure service level agreements are met. Support internal and external audits and represent the Quality department in meetings where required. Ensure QA activities align with VPO requirements. Requirements Degree qualified in a scientific or engineering discipline, or equivalent qualification. Excellent computer, numeracy, literacy and verbal communication skills. Ability to work effectively as part of a team and independently using initiative. Results-focused with strong attention to detail. Strong organisational skills with a structured and systematic approach. Experience contributing to process improvement initiatives. Excellent knowledge of manufacturing principles, tools and techniques. Strong understanding of quality management processes with the ability to coach others. Shift Pattern & Pay 4 on, 4 off rotation. 2 days: 7am-7pm. 2 nights: 7pm-7am. Followed by 4 days off. 22.35 per hour basic rate. Overtime rates: 33.53 per hour for hours worked over 48 between 7am Monday and 7pm Friday. 44.70 per hour for hours worked over 48 between 7pm Friday and 7am Monday. Interested? Apply now with your up-to-date CV or contact your local Acorn by Synergie branch for further information. Acorn by Synergie acts as an employment business for the supply of temporary workers.
Apr 01, 2026
Seasonal
QA Laboratory Technician Magor 22.35- 44.70 per hour 4 on 4 off (2 Days, 2 Nights) Temporary Long-Term Introduction Acorn by Synergie is recruiting a QA Laboratory Technician to join a global brewing company based in Magor. This is a temporary long-term opportunity offering a structured shift pattern, competitive pay rates and overtime opportunities within a fast-paced production environment. Reporting to the QA First Line Manager, you will be responsible for carrying out Quality Assurance analyses across the brewery, ensuring QA policies and procedures are adhered to at all times. You will communicate quality issues to relevant managers and accurately record and report QA data using various software systems. Please note this job description is not exhaustive, and flexibility will be required to undertake reasonable additional duties within your capabilities. Key Duties Deploy existing and new operating practices across the department. Contribute to preventing quality defects reaching customers. Provide QA support across site, responding to quality issues. Monitor performance to ensure specifications, systems and procedures meet product quality and food/feed safety requirements. Undertake routine analysis of samples. Perform calibration and maintenance on laboratory instrumentation. Assist with basic microbiology tasks. Complete required data entry, interpret results and present data at production meetings. Manage hold beer inspections and prepare the taste room for tasting sessions. Train and audit Brewing and Operations staff on QA processes. Participate in root cause analysis and drive process improvements. Contribute to cost optimisation initiatives and departmental projects. Promote safe working practices and ensure compliance with Food Safety, Integrity, Legality and Quality Standards. Maintain departmental SOPs and ensure service level agreements are met. Support internal and external audits and represent the Quality department in meetings where required. Ensure QA activities align with VPO requirements. Requirements Degree qualified in a scientific or engineering discipline, or equivalent qualification. Excellent computer, numeracy, literacy and verbal communication skills. Ability to work effectively as part of a team and independently using initiative. Results-focused with strong attention to detail. Strong organisational skills with a structured and systematic approach. Experience contributing to process improvement initiatives. Excellent knowledge of manufacturing principles, tools and techniques. Strong understanding of quality management processes with the ability to coach others. Shift Pattern & Pay 4 on, 4 off rotation. 2 days: 7am-7pm. 2 nights: 7pm-7am. Followed by 4 days off. 22.35 per hour basic rate. Overtime rates: 33.53 per hour for hours worked over 48 between 7am Monday and 7pm Friday. 44.70 per hour for hours worked over 48 between 7pm Friday and 7am Monday. Interested? Apply now with your up-to-date CV or contact your local Acorn by Synergie branch for further information. Acorn by Synergie acts as an employment business for the supply of temporary workers.
Confidential Opportunity Project Manager Oxford £80,000-£90,000 A well-established, privately owned European construction group is seeking an experienced Project Manager to lead a high-profile commercial fit-out project in Oxford. The business operates across more than 20 countries and is recognised as a leading provider in specialist interior fit-out, building envelope and technical building services solutions. This is a confidential appointment for a flagship project in Oxford, offering the opportunity to join a financially robust, family-owned organisation known for engineering excellence, sustainability and forward-thinking construction methods. The Role As Project Manager, you will take full responsibility for the delivery of a commercial interior fit-out scheme in Oxford from pre-construction through to handover. Key responsibilities include: Leading the project team to deliver safely, on time and within budget Managing subcontractors and supply chain partners Maintaining strong client and consultant relationships Overseeing programme, procurement and cost control Ensuring quality standards and compliance with all HSE requirements Driving value engineering and innovative solutions where appropriate Reporting to senior leadership on project performance About the Company The organisation operates as a full-service provider and manufacturer, delivering: Interior fit-out systems (ceilings, floors, partitions, doors) Cleanroom and laboratory solutions Heated and chilled ceiling systems Facade and building envelope systems Technical building services and insulation Scaffold and specialist engineering solutions About You Proven experience as a Project Manager within commercial fit-out Strong technical understanding of interior systems Experience managing projects typically valued £5m £15m+ Excellent leadership and communication skills Commercially astute with strong programme management capability Degree or equivalent in Construction Management or related discipline (preferred) What s on Offer £80,000 £90,000 salary (DOE) Competitive benefits package Long-term career progression within a stable, international group Opportunity to work on technically challenging, design-led projects
Apr 01, 2026
Full time
Confidential Opportunity Project Manager Oxford £80,000-£90,000 A well-established, privately owned European construction group is seeking an experienced Project Manager to lead a high-profile commercial fit-out project in Oxford. The business operates across more than 20 countries and is recognised as a leading provider in specialist interior fit-out, building envelope and technical building services solutions. This is a confidential appointment for a flagship project in Oxford, offering the opportunity to join a financially robust, family-owned organisation known for engineering excellence, sustainability and forward-thinking construction methods. The Role As Project Manager, you will take full responsibility for the delivery of a commercial interior fit-out scheme in Oxford from pre-construction through to handover. Key responsibilities include: Leading the project team to deliver safely, on time and within budget Managing subcontractors and supply chain partners Maintaining strong client and consultant relationships Overseeing programme, procurement and cost control Ensuring quality standards and compliance with all HSE requirements Driving value engineering and innovative solutions where appropriate Reporting to senior leadership on project performance About the Company The organisation operates as a full-service provider and manufacturer, delivering: Interior fit-out systems (ceilings, floors, partitions, doors) Cleanroom and laboratory solutions Heated and chilled ceiling systems Facade and building envelope systems Technical building services and insulation Scaffold and specialist engineering solutions About You Proven experience as a Project Manager within commercial fit-out Strong technical understanding of interior systems Experience managing projects typically valued £5m £15m+ Excellent leadership and communication skills Commercially astute with strong programme management capability Degree or equivalent in Construction Management or related discipline (preferred) What s on Offer £80,000 £90,000 salary (DOE) Competitive benefits package Long-term career progression within a stable, international group Opportunity to work on technically challenging, design-led projects
Kickstart Your Career as a Trainee Lead Auditor! Location: Doncaster Travel : Yes Full -Time, 2-Year Training Programme Department: Group Quality Reports To: Quality Compliance Manager Are you detail-driven, analytical, and enthusiastic about quality standards? Join SARIA Ltd and become a key part of our mission to maintain excellence in food safety, compliance, and sustainability. We are offering a two-year in-house training programme designed to shape you into a qualified Lead Auditor with access to external courses, firsthand experience , and a guaranteed permanent role at the end of the programme. What You will Be Doing You will be immersed in every aspect of auditing and compliance across our sites from GMP and hygiene audits to supplier approvals and traceability exercises . Your responsibilities will include: Conducting GMP , FSMS/QMS/EMS , and laboratory audits . Supporting supplier approval and external audit activities . Completing gap analyses for key standards such as ISO 9001, FSSC, BRC, and more. Assisting with non-conformance follow-ups and staff training . Driving continuous improvement across the Group Quality Department. What We are Looking For You do not need years of experience we are looking for passion, potential, and precision. Essential: 5 GCSEs (A C) including English and Maths Food Safety Level 2 Strong organisational and communication skills A motivated, initiative-taking attitude with the ability to work to deadlines Desirable: A-Levels or equivalent experience Knowledge of HACCP, traceability, and auditing processes Experience within a quality or manufacturing environment Why Join SARIA? A structured two-year training and development plan Opportunities for external certification and auditing qualifications Mentorship from experienced Quality professionals A pathway to a permanent Lead Auditor role Work within a company that values integrity, innovation, and growth Ready to Take the Lead? If you are ready to build a career in Quality and Compliance and want to learn from the best we would love to hear from you! Apply now and start your journey to becoming a Lead Auditor with SARIA Ltd.
Apr 01, 2026
Full time
Kickstart Your Career as a Trainee Lead Auditor! Location: Doncaster Travel : Yes Full -Time, 2-Year Training Programme Department: Group Quality Reports To: Quality Compliance Manager Are you detail-driven, analytical, and enthusiastic about quality standards? Join SARIA Ltd and become a key part of our mission to maintain excellence in food safety, compliance, and sustainability. We are offering a two-year in-house training programme designed to shape you into a qualified Lead Auditor with access to external courses, firsthand experience , and a guaranteed permanent role at the end of the programme. What You will Be Doing You will be immersed in every aspect of auditing and compliance across our sites from GMP and hygiene audits to supplier approvals and traceability exercises . Your responsibilities will include: Conducting GMP , FSMS/QMS/EMS , and laboratory audits . Supporting supplier approval and external audit activities . Completing gap analyses for key standards such as ISO 9001, FSSC, BRC, and more. Assisting with non-conformance follow-ups and staff training . Driving continuous improvement across the Group Quality Department. What We are Looking For You do not need years of experience we are looking for passion, potential, and precision. Essential: 5 GCSEs (A C) including English and Maths Food Safety Level 2 Strong organisational and communication skills A motivated, initiative-taking attitude with the ability to work to deadlines Desirable: A-Levels or equivalent experience Knowledge of HACCP, traceability, and auditing processes Experience within a quality or manufacturing environment Why Join SARIA? A structured two-year training and development plan Opportunities for external certification and auditing qualifications Mentorship from experienced Quality professionals A pathway to a permanent Lead Auditor role Work within a company that values integrity, innovation, and growth Ready to Take the Lead? If you are ready to build a career in Quality and Compliance and want to learn from the best we would love to hear from you! Apply now and start your journey to becoming a Lead Auditor with SARIA Ltd.
An exciting opportunity has risen for a QC Analyst to join a global pharmaceutical company within their bioassay lab, within QC. Job Title: QC Bioassay Analyst Vacancy type: Temporary role expected to last around 6 months (5 on 3 off shift pattern) Area: Liverpool Salary: Highly competitive SRG is working with a leading global pharmaceutical company who require a QC Bioassay Analyst to join their well-established QC lab. The purpose of the QC Bioassay analyst role is to compliantly perform QC laboratory testing, data review and data interpretation in accordance with approved Standard Operating Procedures (SOPs). Analysis is performed on in-process, intermediate and finished vaccine products. QC Bioassay analysts are also required to participate in technical and validation studies in support of both departmental and site objectives. Responsibilities: The purpose of the QC Incoming and Components Analyst role is to compliantly perform Primary QC inspection, Sampling of raw materials, components laboratory testing, data review and data interpretation in accordance with approved Standard Operating Procedures (SOPs) for all primary and secondary packaging components. QC Incoming and components analysts will be required to support release of raw materials and components for use in manufacture. QC incoming and component's Analysts may also be required to participate in technical and validation studies in support of both departmental and site objectives. Work to a high level of cGMP and GDocP in order to maintain compliance and adherence to regulations. Perform analytical testing of raw materials, in process, finished product and utilities samples in accordance with relevant SOPs. Instrument Maintenance and Calibration Escalate any OOS/OOE/OOT results to Team Co-Ordinator/Laboratory Manager as soon as practically possible. Initiate and perform laboratory investigations with discussion and collaboration with effected departments where necessary. Applicant requirements: BSc in equivalent in Scientific discipline, ideally chemistry. Recent experience in a cGMP pharmaceutical lab performing analytical QC bioassay testing for at least 1 year. SRG are the UK number 1 recruitment company specialising in the science, engineering, clinical, pharmaceutical, food/FMCG, renewable, biotech, chemicals and medical devices sectors. As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients. If you have a scientific background and this position is not relevant / suitable for you please feel free to get in touch or visit (url removed) view our other vacancies. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.
Apr 01, 2026
Seasonal
An exciting opportunity has risen for a QC Analyst to join a global pharmaceutical company within their bioassay lab, within QC. Job Title: QC Bioassay Analyst Vacancy type: Temporary role expected to last around 6 months (5 on 3 off shift pattern) Area: Liverpool Salary: Highly competitive SRG is working with a leading global pharmaceutical company who require a QC Bioassay Analyst to join their well-established QC lab. The purpose of the QC Bioassay analyst role is to compliantly perform QC laboratory testing, data review and data interpretation in accordance with approved Standard Operating Procedures (SOPs). Analysis is performed on in-process, intermediate and finished vaccine products. QC Bioassay analysts are also required to participate in technical and validation studies in support of both departmental and site objectives. Responsibilities: The purpose of the QC Incoming and Components Analyst role is to compliantly perform Primary QC inspection, Sampling of raw materials, components laboratory testing, data review and data interpretation in accordance with approved Standard Operating Procedures (SOPs) for all primary and secondary packaging components. QC Incoming and components analysts will be required to support release of raw materials and components for use in manufacture. QC incoming and component's Analysts may also be required to participate in technical and validation studies in support of both departmental and site objectives. Work to a high level of cGMP and GDocP in order to maintain compliance and adherence to regulations. Perform analytical testing of raw materials, in process, finished product and utilities samples in accordance with relevant SOPs. Instrument Maintenance and Calibration Escalate any OOS/OOE/OOT results to Team Co-Ordinator/Laboratory Manager as soon as practically possible. Initiate and perform laboratory investigations with discussion and collaboration with effected departments where necessary. Applicant requirements: BSc in equivalent in Scientific discipline, ideally chemistry. Recent experience in a cGMP pharmaceutical lab performing analytical QC bioassay testing for at least 1 year. SRG are the UK number 1 recruitment company specialising in the science, engineering, clinical, pharmaceutical, food/FMCG, renewable, biotech, chemicals and medical devices sectors. As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients. If you have a scientific background and this position is not relevant / suitable for you please feel free to get in touch or visit (url removed) view our other vacancies. Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.
Test Solutions Engineer 6 month contract Based in Luton Offering 59ph Inside IR35 Do you have experience with LabVIEW? Do you have experience with configuration management tools such as Teamcenter? Do you want to work with an industry-leading company? If your answers are yes to these, then this could be the role for you! As the Test Solutions Engineer, you will be working alongside a market-leading Defence and Aerospace company who are constantly growing and developing. They are always looking to bring on new talents such as yourself and further develop your skills to enable you to grow within the company and industry. Due to the nature of the work you will be involved in, you will be required to obtain UK SC clearance in this role. You will be involved in: Design & Reviews Prepare and lead joint Test Readiness Reviews (TRR) and Final Qualification Reviews (FQR), ensuring closure of all actions Conduct design reviews for test solutions and drive resolution of associated actions Documentation & Configuration Produce and manage technical documentation required for project delivery, including but not limited to: SDP, TRD, TERs, IDATS, PIC, TSIN, CPs, ABR, ATP, ATR, VDD, user manuals, and logbooks Configure and maintain software and hardware elements to ensure formal test system configuration Software Development & Testing Develop and maintain test software for the automated test platform Generate and manage test limit files, configuration files, and related documentation Debug, commission, and validate test software Conduct ATP investigations and record results in ATR documentation Your skillset may include: Strong experience with NI LabVIEW and/or TestStand Proficiency in Windows environments and Microsoft Office tools Experience with configuration management tools (e.g., Teamcenter or equivalent) Hands-on work within laboratory environments If this all sounds like something you will be interested in then simply apply and we can discuss the opportunity further! Test Solutions Engineer 6 month contract Based in Luton Offering 59ph Inside IR35 Disclaimer: This vacancy is being advertised by either Advanced Resource Managers Limited, Advanced Resource Managers IT Limited or Advanced Resource Managers Engineering Limited ("ARM"). ARM is a specialist talent acquisition and management consultancy. We provide technical contingency recruitment and a portfolio of more complex resource solutions. Our specialist recruitment divisions cover the entire technical arena, including some of the most economically and strategically important industries in the UK and the world today. We will never send your CV without your permission. Where the role is marked as Outside IR35 in the advertisement this is subject to receipt of a final Status Determination Statement from the end Client and may be subject to change.
Mar 31, 2026
Contractor
Test Solutions Engineer 6 month contract Based in Luton Offering 59ph Inside IR35 Do you have experience with LabVIEW? Do you have experience with configuration management tools such as Teamcenter? Do you want to work with an industry-leading company? If your answers are yes to these, then this could be the role for you! As the Test Solutions Engineer, you will be working alongside a market-leading Defence and Aerospace company who are constantly growing and developing. They are always looking to bring on new talents such as yourself and further develop your skills to enable you to grow within the company and industry. Due to the nature of the work you will be involved in, you will be required to obtain UK SC clearance in this role. You will be involved in: Design & Reviews Prepare and lead joint Test Readiness Reviews (TRR) and Final Qualification Reviews (FQR), ensuring closure of all actions Conduct design reviews for test solutions and drive resolution of associated actions Documentation & Configuration Produce and manage technical documentation required for project delivery, including but not limited to: SDP, TRD, TERs, IDATS, PIC, TSIN, CPs, ABR, ATP, ATR, VDD, user manuals, and logbooks Configure and maintain software and hardware elements to ensure formal test system configuration Software Development & Testing Develop and maintain test software for the automated test platform Generate and manage test limit files, configuration files, and related documentation Debug, commission, and validate test software Conduct ATP investigations and record results in ATR documentation Your skillset may include: Strong experience with NI LabVIEW and/or TestStand Proficiency in Windows environments and Microsoft Office tools Experience with configuration management tools (e.g., Teamcenter or equivalent) Hands-on work within laboratory environments If this all sounds like something you will be interested in then simply apply and we can discuss the opportunity further! Test Solutions Engineer 6 month contract Based in Luton Offering 59ph Inside IR35 Disclaimer: This vacancy is being advertised by either Advanced Resource Managers Limited, Advanced Resource Managers IT Limited or Advanced Resource Managers Engineering Limited ("ARM"). ARM is a specialist talent acquisition and management consultancy. We provide technical contingency recruitment and a portfolio of more complex resource solutions. Our specialist recruitment divisions cover the entire technical arena, including some of the most economically and strategically important industries in the UK and the world today. We will never send your CV without your permission. Where the role is marked as Outside IR35 in the advertisement this is subject to receipt of a final Status Determination Statement from the end Client and may be subject to change.
Role: Technical Manager / Quality Manager Salary: 60,000 to 90,000 per annum plus Bonus, Car Allowance (or Company Car), Private & Family Medical, Life Assurance, 25 Days Holiday plus 8 Bank Holidays, Pension, and additional Benefits Hours: 8am to 5pm, Monday to Friday with flexible start and finish times Location: UK wide travel required with a preference for Midlands based candidates Company We are recruiting for a reputable multi-site manufacturer who are looking to appoint a Technical Manager as part of their succession planning. The business is dedicated to supporting and creating a more sustainable future through a range of high-quality products, systems, and solutions. We are seeking a strong leader with proven people management and compliance experience to take on a pivotal role, helping to shape product quality, sustainability, and long-term reliability across the business. This is an excellent opportunity for someone who enjoys responsibility, challenge and the ability to influence strategy and direction within a national technical function. The Role You will oversee the Technical Department across UK operations, managing multiple sites, laboratories, and a team of up to 15 technical staff. The role covers the full lifecycle of materials strategy, from sourcing and approving raw materials through to laboratory oversight and ensuring product compliance across all sites. This is a regional position covering the UK and Ireland. Regular travel and overnight stays will be required. Key responsibilities include: Maintaining safety, quality, and sustainability standards across all sites Driving research, development, and innovation initiatives Supporting strategic decision-making across operations Providing senior leadership and representing the business externally Acting as the primary quality liaison with customers, suppliers, and external bodies Managing complaints, non-conformances and supplier issues through to root cause and resolution Implementing and driving continuous improvement across the business Requirements Proven experience as a Technical Manager or Quality Manager at department level Background within ceramics, aggregates, quarrying or similar materials environments Strong experience in materials management, product development and compliance Laboratory experience Hands-on leadership approach Strong root cause analysis and continuous improvement experience Ideally qualified in Ceramic Engineering or a related discipline Application If this role is of interest, please apply with your most up to date CV or contact Wesley at TechNichols Resourcing for a confidential discussion. We aim to respond to all applicants within 5 working days. If you have not heard from us within this time, your application has unfortunately been unsuccessful.
Mar 31, 2026
Full time
Role: Technical Manager / Quality Manager Salary: 60,000 to 90,000 per annum plus Bonus, Car Allowance (or Company Car), Private & Family Medical, Life Assurance, 25 Days Holiday plus 8 Bank Holidays, Pension, and additional Benefits Hours: 8am to 5pm, Monday to Friday with flexible start and finish times Location: UK wide travel required with a preference for Midlands based candidates Company We are recruiting for a reputable multi-site manufacturer who are looking to appoint a Technical Manager as part of their succession planning. The business is dedicated to supporting and creating a more sustainable future through a range of high-quality products, systems, and solutions. We are seeking a strong leader with proven people management and compliance experience to take on a pivotal role, helping to shape product quality, sustainability, and long-term reliability across the business. This is an excellent opportunity for someone who enjoys responsibility, challenge and the ability to influence strategy and direction within a national technical function. The Role You will oversee the Technical Department across UK operations, managing multiple sites, laboratories, and a team of up to 15 technical staff. The role covers the full lifecycle of materials strategy, from sourcing and approving raw materials through to laboratory oversight and ensuring product compliance across all sites. This is a regional position covering the UK and Ireland. Regular travel and overnight stays will be required. Key responsibilities include: Maintaining safety, quality, and sustainability standards across all sites Driving research, development, and innovation initiatives Supporting strategic decision-making across operations Providing senior leadership and representing the business externally Acting as the primary quality liaison with customers, suppliers, and external bodies Managing complaints, non-conformances and supplier issues through to root cause and resolution Implementing and driving continuous improvement across the business Requirements Proven experience as a Technical Manager or Quality Manager at department level Background within ceramics, aggregates, quarrying or similar materials environments Strong experience in materials management, product development and compliance Laboratory experience Hands-on leadership approach Strong root cause analysis and continuous improvement experience Ideally qualified in Ceramic Engineering or a related discipline Application If this role is of interest, please apply with your most up to date CV or contact Wesley at TechNichols Resourcing for a confidential discussion. We aim to respond to all applicants within 5 working days. If you have not heard from us within this time, your application has unfortunately been unsuccessful.
Our client is a successful and well-established manufacturer. They are looking for a Compliance Manager to take responsibilty for Safety, Health, Environmental and Quality compliance on a permanent basis. Your main responsibilities will include ensuring products and services are manufactured and delivered effectively, efficiently, on-time, to specification, and in a cost-effective manner. This role will include full responsibility for ISO9001 programme/quality control functions; Health & Safety, all weld metallurgy in the manufacture of the company s products. PLEASE ONLY APPLY IF YOU MEET THE FOLLOWING CRITERIA: You have experience of working extensively with Metals / Metallurgy. You are NEBOSH and/or IOSH qualified. You have experience of working to ISO9001. You have experience of managing people/have had direct reports to manage. You have experience of working with both Health & Safety and Quality Assurance within a manufacturing environment (preferably for a metal product manufacturing company, or industrial products). Salary: Up to £53,000 depending on experience. Hours of work: Monday to Thursday 8.00am - 5.00pm, Friday 8.00am 1.00pm. Duties: To assume head departmental responsibility for ISO9001, Health and Safety and Metallurgy functions on site. Manage the business to ensure the ISO9001:2015 accreditation is maintained. Manage all aspects of goods inwards, in process and final quality inspection within the business to support manufacturing output in line with the Financial budget, To contribute with the completion of supplier/internal reject quality documentation and completion of associated Performance Improvement reports (PIR s). Manage all internal rework identification and issuing including methods to ensure it is completed in the most expedient and cost effective manner possible. Manage Customer complaints by understanding the issues, addressing the corrective action and ensuring the customer is communicated to throughout the process. Manage in house inspection resources to support the achievement of the company s customer service deadlines and OTIF delivery targets. Manage the annual calibration and recording of all measuring equipment for manufacturing and quality control. To ensure that any accidents/near misses are investigated thoroughly and within the associated timeframe resulting in corrective actions being in place with the manufacturing team. Review and update Risk assessments and Method statements to underpin the training matrices for all employees to ensure all employees have received adequate training to perform tasks and run machines with supporting signed RAMS documentation. To develop and produce internal Welding procedure specification (WPS). To ensure that all manufacturing is QC checked in line with current ISO Work Instructions. Manage the metallurgical and laboratory functions to ensure plate manufacturing is controlled within the business from a quality and productivity perspective. To adapt and to take on board any future requests or tasks as reasonably requested from time to time. This role would suit someone with experience in both Quality and Health & Safety at a manufacturer, roles such as; Health & Safety Quality Advisor / SHEQ Manager / SHEQ Supervisor / HSQE Manager / HSEQ Manager / QHSE Manager / Health Safety and Environmental Advisor / H&S Co-ordinator / HSE Officer / Health Safety and Environmental Advisor / Quality Assurance Manager / Quality Controller / QC Manager / QA Manager / QC Manager / QC Manager / HSE Manager / QESH Manager / Health & Safety Lead / etc.
Mar 31, 2026
Full time
Our client is a successful and well-established manufacturer. They are looking for a Compliance Manager to take responsibilty for Safety, Health, Environmental and Quality compliance on a permanent basis. Your main responsibilities will include ensuring products and services are manufactured and delivered effectively, efficiently, on-time, to specification, and in a cost-effective manner. This role will include full responsibility for ISO9001 programme/quality control functions; Health & Safety, all weld metallurgy in the manufacture of the company s products. PLEASE ONLY APPLY IF YOU MEET THE FOLLOWING CRITERIA: You have experience of working extensively with Metals / Metallurgy. You are NEBOSH and/or IOSH qualified. You have experience of working to ISO9001. You have experience of managing people/have had direct reports to manage. You have experience of working with both Health & Safety and Quality Assurance within a manufacturing environment (preferably for a metal product manufacturing company, or industrial products). Salary: Up to £53,000 depending on experience. Hours of work: Monday to Thursday 8.00am - 5.00pm, Friday 8.00am 1.00pm. Duties: To assume head departmental responsibility for ISO9001, Health and Safety and Metallurgy functions on site. Manage the business to ensure the ISO9001:2015 accreditation is maintained. Manage all aspects of goods inwards, in process and final quality inspection within the business to support manufacturing output in line with the Financial budget, To contribute with the completion of supplier/internal reject quality documentation and completion of associated Performance Improvement reports (PIR s). Manage all internal rework identification and issuing including methods to ensure it is completed in the most expedient and cost effective manner possible. Manage Customer complaints by understanding the issues, addressing the corrective action and ensuring the customer is communicated to throughout the process. Manage in house inspection resources to support the achievement of the company s customer service deadlines and OTIF delivery targets. Manage the annual calibration and recording of all measuring equipment for manufacturing and quality control. To ensure that any accidents/near misses are investigated thoroughly and within the associated timeframe resulting in corrective actions being in place with the manufacturing team. Review and update Risk assessments and Method statements to underpin the training matrices for all employees to ensure all employees have received adequate training to perform tasks and run machines with supporting signed RAMS documentation. To develop and produce internal Welding procedure specification (WPS). To ensure that all manufacturing is QC checked in line with current ISO Work Instructions. Manage the metallurgical and laboratory functions to ensure plate manufacturing is controlled within the business from a quality and productivity perspective. To adapt and to take on board any future requests or tasks as reasonably requested from time to time. This role would suit someone with experience in both Quality and Health & Safety at a manufacturer, roles such as; Health & Safety Quality Advisor / SHEQ Manager / SHEQ Supervisor / HSQE Manager / HSEQ Manager / QHSE Manager / Health Safety and Environmental Advisor / H&S Co-ordinator / HSE Officer / Health Safety and Environmental Advisor / Quality Assurance Manager / Quality Controller / QC Manager / QA Manager / QC Manager / QC Manager / HSE Manager / QESH Manager / Health & Safety Lead / etc.
Caresoft Global Talent Solutions Ltd
City, Wolverhampton
Job Title: Laboratory Tech Analysis - Technician ( Metallurgy and Materials) Location: Wolverhampton EMC (WV9 5GA) Rate: £21.88ph via an Umbrella Company (Inside IR35) or £16.42 on a PAYE basis Employment Type: Contract (Financed until September 2026) Hours: Standard 39 Hours Per Week Monday to Friday, over alternating 2 shifts. Early shift 06:00 - 14:00 (M-T), 06:00 - 13:00 (F). Late shift 14:00 - 22:00 (M-T), 13:00 - 20:00 (F). Duties: Use metallurgical & mechanical preparation and test equipment to assess components according to standard test processes, as required by engineering specifications or drawings. Carry out routine quality control testing for EDU, Battery and Frame Assembly. Perform teardowns of stators and frames, using destructive equipment, e.g. Bandsaws. Perform visual weld inspection testing and ultrasonic testing of spot welds. Use optical microscopes to measure welds, rivets and porosity content. Perform radiographic analysis of components. Support investigation of product quality issues with cross functional teams. Ensure internal and external audit compliance to standards including IATF 16949 and ISO 14001. Compliance to Health and Safety procedures by ensuring all safety metrics are achieved, including identifying safety hazards and risks and supporting implementation of corrective action. Adhere to local working documents and lab practises, e.g. 5S, Local Work Instructions, Autonomous Maintenance Tasks, Risk & COSHH assessments. Undertake any other work as directed by their line manager in connection with their job as may be requested . Skills: Essential Experienced in using preparation equipment (e.g. bandsaws, abrasive cutters, grinding, polishing, etching). Previous experience incorporating knowledge and practical operation of materials testing equipment (optical microscopes, hardness, tensile, composition, cleanliness, FTIR, OES, DSC, RFU. Etc). Metallurgical knowledge of steel and aluminium, and experience in applying this know-how. Able to interpret Engineering drawings and Specifications. Computer skills experienced using Excel, Word and PowerPoint. Desirable Previous experience in interpreting X-Rays and CT scans. A working knowledge of welding (MIG/TIG/CMT). CSWIP weld inspection experience. Use of ultrasonic equipment/PAUT for spot weld measurement. Education: Required: Minimum level 3 qualification in a relevant engineering, science or welding field. Desirable: Ultrasonic/PAUT level 2 qualified CSWIP Visual Weld Inspector qualified Additional information: Will be required to work 39hr working week. M - F, over alternating 2 shifts. Early shift 06:00 - 14:00 (M-T), 06:00 - 13:00 (F). Late shift 14:00 - 22:00 (M-T), 13:00 - 20:00 (F). THIS POSITION IS INSIDE IR35 Do not miss out on your chance of interview APPLY NOW! Our Clients are unable to provide sponsorship for Visas; therefore, only candidates eligible to work in the UK need apply! Caresoft Global Talent Solutions operates as an Employment Business and Employment Agency. We are an independent highly-experienced recruitment consultancy dedicated to specialist markets within the Automotive, Aerospace, Agricultural & Construction Industries. No terminology within this advert is intended to unlawfully discriminate on the grounds of age, sex, race or disability and we welcome all applications.
Mar 31, 2026
Contractor
Job Title: Laboratory Tech Analysis - Technician ( Metallurgy and Materials) Location: Wolverhampton EMC (WV9 5GA) Rate: £21.88ph via an Umbrella Company (Inside IR35) or £16.42 on a PAYE basis Employment Type: Contract (Financed until September 2026) Hours: Standard 39 Hours Per Week Monday to Friday, over alternating 2 shifts. Early shift 06:00 - 14:00 (M-T), 06:00 - 13:00 (F). Late shift 14:00 - 22:00 (M-T), 13:00 - 20:00 (F). Duties: Use metallurgical & mechanical preparation and test equipment to assess components according to standard test processes, as required by engineering specifications or drawings. Carry out routine quality control testing for EDU, Battery and Frame Assembly. Perform teardowns of stators and frames, using destructive equipment, e.g. Bandsaws. Perform visual weld inspection testing and ultrasonic testing of spot welds. Use optical microscopes to measure welds, rivets and porosity content. Perform radiographic analysis of components. Support investigation of product quality issues with cross functional teams. Ensure internal and external audit compliance to standards including IATF 16949 and ISO 14001. Compliance to Health and Safety procedures by ensuring all safety metrics are achieved, including identifying safety hazards and risks and supporting implementation of corrective action. Adhere to local working documents and lab practises, e.g. 5S, Local Work Instructions, Autonomous Maintenance Tasks, Risk & COSHH assessments. Undertake any other work as directed by their line manager in connection with their job as may be requested . Skills: Essential Experienced in using preparation equipment (e.g. bandsaws, abrasive cutters, grinding, polishing, etching). Previous experience incorporating knowledge and practical operation of materials testing equipment (optical microscopes, hardness, tensile, composition, cleanliness, FTIR, OES, DSC, RFU. Etc). Metallurgical knowledge of steel and aluminium, and experience in applying this know-how. Able to interpret Engineering drawings and Specifications. Computer skills experienced using Excel, Word and PowerPoint. Desirable Previous experience in interpreting X-Rays and CT scans. A working knowledge of welding (MIG/TIG/CMT). CSWIP weld inspection experience. Use of ultrasonic equipment/PAUT for spot weld measurement. Education: Required: Minimum level 3 qualification in a relevant engineering, science or welding field. Desirable: Ultrasonic/PAUT level 2 qualified CSWIP Visual Weld Inspector qualified Additional information: Will be required to work 39hr working week. M - F, over alternating 2 shifts. Early shift 06:00 - 14:00 (M-T), 06:00 - 13:00 (F). Late shift 14:00 - 22:00 (M-T), 13:00 - 20:00 (F). THIS POSITION IS INSIDE IR35 Do not miss out on your chance of interview APPLY NOW! Our Clients are unable to provide sponsorship for Visas; therefore, only candidates eligible to work in the UK need apply! Caresoft Global Talent Solutions operates as an Employment Business and Employment Agency. We are an independent highly-experienced recruitment consultancy dedicated to specialist markets within the Automotive, Aerospace, Agricultural & Construction Industries. No terminology within this advert is intended to unlawfully discriminate on the grounds of age, sex, race or disability and we welcome all applications.
Do you want to take the next step in your Biomedical Science career within one of Northern Ireland's busiest laboratory environments? MCS Group is delighted to be recruiting on behalf of the Royal Victoria Hospital for a Band 6 Cellular Pathology Biomedical Scientist , joining a high-performing service on a long term contract. This is an excellent opportunity to contribute to a specialist pathology discipline within a major regional hospital, supporting timely diagnostics and high quality patient care within a fast-paced, highly skilled team. The Role As a Band 6 Biomedical Scientist in Cellular Pathology , you will: Perform a full range of specialist Cellular Pathology techniques in line with laboratory protocols and professional standards. Process, embed, cut, stain and analyse tissue samples ensuring accuracy, quality and turnaround times are maintained. Participate in specialist techniques such as immunohistochemistry, frozen sections and advanced staining methods as required. Ensure all work meets UKAS, ISO15189 and local quality management standards. Contribute to troubleshooting, continuous service improvement and development of laboratory processes. Maintain high levels of documentation, quality records and compliance data. Provide technical support, guidance and training to junior laboratory staff when required. Work effectively within a multidisciplinary laboratory environment, supporting consultants, lab managers and clinical teams. This role offers exposure to a wide caseload, modern equipment and the chance to further develop specialist Cellular Pathology expertise within a leading regional centre. Essential Criteria Applicants must: Be HCPC registered as a Biomedical Scientist. Hold a relevant Biomedical Science degree (or equivalent). Have significant experience working within Cellular Pathology at Band 5/6 level. Be fully competent in core histology techniques including microtomy, embedding, staining and tissue processing. Demonstrate strong knowledge of laboratory safety, quality systems and ISO15189 standards. Communicate effectively and work confidently within a busy diagnostic environment. Why This Role? Work within one of NI's major hospital laboratories. Long term contractual stability. Access to modern histology equipment and a wide ranging specialist workload. Supportive, skilled team environment with opportunities for development and upskilling. To speak in absolute confidence about this opportunity, please send an up to date CV via the link provided or contact Zachery Downes, Specialist Recruitment Consultant , for a confidential discussion. This position is subject to standard Access NI pre employment checks. A criminal record will not necessarily be a bar to obtaining the position. We are committed to Equality, Diversity and Inclusion and welcome applications from all suitably qualified individuals. If you require reasonable adjustments at any stage of the recruitment process, please let us know. Even if this position isn't right for you, we may have others that are. Get in touch to discuss your options.
Mar 30, 2026
Full time
Do you want to take the next step in your Biomedical Science career within one of Northern Ireland's busiest laboratory environments? MCS Group is delighted to be recruiting on behalf of the Royal Victoria Hospital for a Band 6 Cellular Pathology Biomedical Scientist , joining a high-performing service on a long term contract. This is an excellent opportunity to contribute to a specialist pathology discipline within a major regional hospital, supporting timely diagnostics and high quality patient care within a fast-paced, highly skilled team. The Role As a Band 6 Biomedical Scientist in Cellular Pathology , you will: Perform a full range of specialist Cellular Pathology techniques in line with laboratory protocols and professional standards. Process, embed, cut, stain and analyse tissue samples ensuring accuracy, quality and turnaround times are maintained. Participate in specialist techniques such as immunohistochemistry, frozen sections and advanced staining methods as required. Ensure all work meets UKAS, ISO15189 and local quality management standards. Contribute to troubleshooting, continuous service improvement and development of laboratory processes. Maintain high levels of documentation, quality records and compliance data. Provide technical support, guidance and training to junior laboratory staff when required. Work effectively within a multidisciplinary laboratory environment, supporting consultants, lab managers and clinical teams. This role offers exposure to a wide caseload, modern equipment and the chance to further develop specialist Cellular Pathology expertise within a leading regional centre. Essential Criteria Applicants must: Be HCPC registered as a Biomedical Scientist. Hold a relevant Biomedical Science degree (or equivalent). Have significant experience working within Cellular Pathology at Band 5/6 level. Be fully competent in core histology techniques including microtomy, embedding, staining and tissue processing. Demonstrate strong knowledge of laboratory safety, quality systems and ISO15189 standards. Communicate effectively and work confidently within a busy diagnostic environment. Why This Role? Work within one of NI's major hospital laboratories. Long term contractual stability. Access to modern histology equipment and a wide ranging specialist workload. Supportive, skilled team environment with opportunities for development and upskilling. To speak in absolute confidence about this opportunity, please send an up to date CV via the link provided or contact Zachery Downes, Specialist Recruitment Consultant , for a confidential discussion. This position is subject to standard Access NI pre employment checks. A criminal record will not necessarily be a bar to obtaining the position. We are committed to Equality, Diversity and Inclusion and welcome applications from all suitably qualified individuals. If you require reasonable adjustments at any stage of the recruitment process, please let us know. Even if this position isn't right for you, we may have others that are. Get in touch to discuss your options.
The High School Science Lab Technician supports the science faculty in delivering high-quality, hands-on learning experiences by preparing, setting up and taking down laboratory equipment and materials, maintaining science supplies and inventory, and ensuring a safe and organized laboratory environment. Working collaboratively with the other lab technician, this role is essential to enabling effective science instruction and fostering student exploration and innovation in alignment with ASL's commitment to developing thinkers, explorers, and innovators. Summary of Duties Laboratory Preparation and Support Provide technical support to Science teachers by preparing, setting up, and taking down laboratory exercises and equipment as requested Assemble and disassemble equipment necessary for science experiments and activities, mixing solutions and chemicals as required for all courses Prepare labs and solutions for the Middle School and/or Lower School when reasonably requested Assist and support faculty during lessons when requested Safety and Compliance Conduct daily checks of classroom and departmental IT equipment, gas provision, and chemical storage, ensuring the overall safety of the laboratories at all times Conduct and write risk assessments for laboratory experiments and practical assignments, liaising with the Health and Safety Manager Maintain chemical storage and ensure the safe use of chemicals and dangerous substances, adhering to COSHH assessments and CLEAPSS requirements Ensure safe disposal and recycling of chemical waste and materials when necessary, maintaining a safe working environment for students and staff Equipment and Inventory Management Repair and maintain lab equipment, advising the Head of Department when new equipment or outside repairs are needed Order materials and supplies as required and in consultation with the Head of Department. Manage laboratory-specific tasks, including opening and locking up laboratories, laptops, and chemical storage Clean laboratory equipment after use when safe handling is required, and maintain record keeping of equipment Professional Development and Innovation Work alongside faculty to devise, develop, and implement new lab exercises, advising on technical developments in the scientific field Research and attend necessary Continuing Professional Development (CPD) courses to stay abreast of new trends, practices, and procedures in science teaching and technology School Community Engagement Participate actively in the life of the School through attendance at events, committee membership, and/or leadership of extracurricular activities Any other duties as are within the scope, spirit, and purpose of the job as requested by the HS Science Department Head or Divisional Principal Selection criteria Essential qualifications/experience A qualification in science technology or similar Experience working and/or studying in a science laboratory or similar environment Demonstrably strong organizational abilities, along with excellent oral and written communication skills Outstanding collaborative skills and a desire to work in a team-focused environment A proven commitment to the safeguarding and welfare of children Desirable qualifications/experience Experience working in a school or other educational setting A good working knowledge of fire and health and safety regulations, especially in relation to COSHH and CLEAPSS Knowledge and understanding of international and/or independent school communities
Mar 30, 2026
Full time
The High School Science Lab Technician supports the science faculty in delivering high-quality, hands-on learning experiences by preparing, setting up and taking down laboratory equipment and materials, maintaining science supplies and inventory, and ensuring a safe and organized laboratory environment. Working collaboratively with the other lab technician, this role is essential to enabling effective science instruction and fostering student exploration and innovation in alignment with ASL's commitment to developing thinkers, explorers, and innovators. Summary of Duties Laboratory Preparation and Support Provide technical support to Science teachers by preparing, setting up, and taking down laboratory exercises and equipment as requested Assemble and disassemble equipment necessary for science experiments and activities, mixing solutions and chemicals as required for all courses Prepare labs and solutions for the Middle School and/or Lower School when reasonably requested Assist and support faculty during lessons when requested Safety and Compliance Conduct daily checks of classroom and departmental IT equipment, gas provision, and chemical storage, ensuring the overall safety of the laboratories at all times Conduct and write risk assessments for laboratory experiments and practical assignments, liaising with the Health and Safety Manager Maintain chemical storage and ensure the safe use of chemicals and dangerous substances, adhering to COSHH assessments and CLEAPSS requirements Ensure safe disposal and recycling of chemical waste and materials when necessary, maintaining a safe working environment for students and staff Equipment and Inventory Management Repair and maintain lab equipment, advising the Head of Department when new equipment or outside repairs are needed Order materials and supplies as required and in consultation with the Head of Department. Manage laboratory-specific tasks, including opening and locking up laboratories, laptops, and chemical storage Clean laboratory equipment after use when safe handling is required, and maintain record keeping of equipment Professional Development and Innovation Work alongside faculty to devise, develop, and implement new lab exercises, advising on technical developments in the scientific field Research and attend necessary Continuing Professional Development (CPD) courses to stay abreast of new trends, practices, and procedures in science teaching and technology School Community Engagement Participate actively in the life of the School through attendance at events, committee membership, and/or leadership of extracurricular activities Any other duties as are within the scope, spirit, and purpose of the job as requested by the HS Science Department Head or Divisional Principal Selection criteria Essential qualifications/experience A qualification in science technology or similar Experience working and/or studying in a science laboratory or similar environment Demonstrably strong organizational abilities, along with excellent oral and written communication skills Outstanding collaborative skills and a desire to work in a team-focused environment A proven commitment to the safeguarding and welfare of children Desirable qualifications/experience Experience working in a school or other educational setting A good working knowledge of fire and health and safety regulations, especially in relation to COSHH and CLEAPSS Knowledge and understanding of international and/or independent school communities
About the Role The overseeing of day-to-day operations in the laboratory, ensuring Turn around times and on time delivery expectations are met. Responsible for ensuring the precision and accuracy of all measurements made in the laboratory Manage all calibration activities, including the management of in-house test equipment, back to preferred suppliers click apply for full job details
Mar 30, 2026
Full time
About the Role The overseeing of day-to-day operations in the laboratory, ensuring Turn around times and on time delivery expectations are met. Responsible for ensuring the precision and accuracy of all measurements made in the laboratory Manage all calibration activities, including the management of in-house test equipment, back to preferred suppliers click apply for full job details
Job Title: Laboratory Technician Location: Kettering Reports to: Plant Quality Laboratory Manager Salary: £31,626.90 (during probation), increasing to £32,076.24 post-probation Contract: 12-month fixed-term contract Working Hours: Thursday-Sunday (working on Saturday and Sunday is required as part of weekend cover), with flexibility for remaining days worked in the week i click apply for full job details
Mar 27, 2026
Contractor
Job Title: Laboratory Technician Location: Kettering Reports to: Plant Quality Laboratory Manager Salary: £31,626.90 (during probation), increasing to £32,076.24 post-probation Contract: 12-month fixed-term contract Working Hours: Thursday-Sunday (working on Saturday and Sunday is required as part of weekend cover), with flexibility for remaining days worked in the week i click apply for full job details
Program/Project Managers - Labs, R&D, - UK/Europe, Hybrid A large global organization are looking for Project & Programme Managers to assist in a Lab Transformation practice, that brings together scientific innovation and advanced digital technologies to modernize laboratory operations. The role will be a full time permanent position which can be worked on a hybrid basis. Candidates can be based from the UK or any location across Europe. Key Responsibilities: Advise and oversee the delivery of digital laboratory solutions including LIMS, ELN, CDS, SDMS, AI/GenAI, IoT, analytics, and cloud Lead, inspire, and mentor high-performing teams and fellow leaders Shape thought leadership to strengthen our brand and industry presence Define and drive strategic vision across people, process, technology, and data Oversee delivery of complex engagements from strategy through execution Build and maintain strong, long-term client relationships Ensure accountability for client outcomes and contractual commitments Articulate compelling value propositions and develop robust business cases What we're looking for: Proven leadership experience in consulting, lab transformation, or digital/technology-enabled environments Strong understanding of laboratory operations, scientific workflows, or lab informatics Experience delivering large-scale, complex transformation programs Ability to bridge business strategy with technology implementation Exceptional stakeholder management and communication skills Passion for innovation and emerging technologies (AI, automation, IoT, cloud, analytics) Background from Pharmaceutical, Life Sciences or Manufacturing is a plus Program/Project Managers - Labs, R&D, - UK/Europe, Hybrid
Mar 26, 2026
Full time
Program/Project Managers - Labs, R&D, - UK/Europe, Hybrid A large global organization are looking for Project & Programme Managers to assist in a Lab Transformation practice, that brings together scientific innovation and advanced digital technologies to modernize laboratory operations. The role will be a full time permanent position which can be worked on a hybrid basis. Candidates can be based from the UK or any location across Europe. Key Responsibilities: Advise and oversee the delivery of digital laboratory solutions including LIMS, ELN, CDS, SDMS, AI/GenAI, IoT, analytics, and cloud Lead, inspire, and mentor high-performing teams and fellow leaders Shape thought leadership to strengthen our brand and industry presence Define and drive strategic vision across people, process, technology, and data Oversee delivery of complex engagements from strategy through execution Build and maintain strong, long-term client relationships Ensure accountability for client outcomes and contractual commitments Articulate compelling value propositions and develop robust business cases What we're looking for: Proven leadership experience in consulting, lab transformation, or digital/technology-enabled environments Strong understanding of laboratory operations, scientific workflows, or lab informatics Experience delivering large-scale, complex transformation programs Ability to bridge business strategy with technology implementation Exceptional stakeholder management and communication skills Passion for innovation and emerging technologies (AI, automation, IoT, cloud, analytics) Background from Pharmaceutical, Life Sciences or Manufacturing is a plus Program/Project Managers - Labs, R&D, - UK/Europe, Hybrid
CTSEurope Ltd Containment Technology Services specialise in the design, construction and commissioning of Laboratory Containment Systems for handling pharmaceutical drug compounds. Our products are unique and award winning, including the Queens Award for Innovation. We are proud to base our operations, including manufacturing in Portsmouth click apply for full job details
Mar 25, 2026
Full time
CTSEurope Ltd Containment Technology Services specialise in the design, construction and commissioning of Laboratory Containment Systems for handling pharmaceutical drug compounds. Our products are unique and award winning, including the Queens Award for Innovation. We are proud to base our operations, including manufacturing in Portsmouth click apply for full job details