A leading materials science firm in the UK is offering a Materials Science Technologist apprenticeship. This role provides hands-on experience in R&D with a focus on cutting-edge magnesium alloys and zirconium materials. You'll conduct mechanical testing, work closely with various departments, and gain a fully accredited degree through a structured training programme. Ideal candidates are motivated individuals with strong communication and organization skills. A competitive salary of £18,000 plus benefits is offered, along with a supportive working environment.
May 02, 2026
Full time
A leading materials science firm in the UK is offering a Materials Science Technologist apprenticeship. This role provides hands-on experience in R&D with a focus on cutting-edge magnesium alloys and zirconium materials. You'll conduct mechanical testing, work closely with various departments, and gain a fully accredited degree through a structured training programme. Ideal candidates are motivated individuals with strong communication and organization skills. A competitive salary of £18,000 plus benefits is offered, along with a supportive working environment.
A leading tech company in the UK is seeking a Materials Laboratory Scientist specializing in thin films. In this role, you will develop innovative thin-film materials and collaborate with computational scientists and engineers. The ideal candidate will hold a PhD and have substantial experience in thin-film synthesis and characterization. This position is part of an exciting initiative aimed at integrating AI predictions with materials research, fostering advancements in technology and science.
May 02, 2026
Full time
A leading tech company in the UK is seeking a Materials Laboratory Scientist specializing in thin films. In this role, you will develop innovative thin-film materials and collaborate with computational scientists and engineers. The ideal candidate will hold a PhD and have substantial experience in thin-film synthesis and characterization. This position is part of an exciting initiative aimed at integrating AI predictions with materials research, fostering advancements in technology and science.
OVERVIEW Merrick & Company, an employee owned company, is seeking an experienced Senior Scientist in Biosafety and Laboratory Operations to join our growing team. The person would become a crucial part of a key Merrick growth initiative in Life Sciences, Biosafety & Biosecurity, and Laboratory Operations markets. This position is open for work in London, with ability to travel to client sites across the UK and Europe. The Scientist must be capable of coordinating and supporting a multi faced series of projects related to laboratory operations, operational planning, biosafety & biosecurity, regulatory compliance, and the integration of consensus standards (e.g., ANSI, ASHRAE), manufacturers use instructions, and industry best practices. This person would support the Science & Technology team with duties and coordination as part of a team of scientists, engineers, and subject matter experts. The position will work interactively with other teams responsible for laboratory design, commissioning, and operational planning, development of laboratory IT and IS systems, and development of laboratory programs (e.g., clinical, diagnostic, and research safety, bio risk management, small to large animal laboratory issues, etc.). This position requires the ability to not only be proficient in biosafety, but also clinical and research laboratory operations with an understanding of how laboratory activities, controls, and equipment function to support the containment and isolation of laboratory hazards. This person will support development of high level technical products and deliverables, problem solving and planning for high visibility projects, and as such must possess excellent communication skills. This position requires a high level of demonstrated effectiveness in working with HM government entities, regulators, and academic, clinical, and academic administrators, internal team members and outside consulting team members. The successful candidate will be required to interface with a broad spectrum of clients for Life Sciences projects located anywhere within the UK. Moderate travel (up to 50%) may be required. WHAT YOU'LL DO Provide strategy, development, execution, and technical knowledge for project deliverables related to laboratory operations, biological risk identification, assessment, characterization, management, exposure assessment and control, general safety, occupational hygiene, health and environmental management, animal care and use and regulatory compliance. Possess strong oral and written communications and interpersonal skills to effectively interface with clients and team members to: Ensure adherence to project quality of deliverables, products, and schedule Address issues related to the interface of laboratory operations, compliance, and operational planning Prepare complex studies, reports, plans, specifications, and other products for project deliverables. Support document preparation to aid clients in obtaining and maintaining regulatory registrations and permits. Support proposal development and marketing initiatives. Support leadership to ensure that project schedules and budgets are met and communicate with leadership any issues and concerns. Exercise initiative, judgment, and knowledge commensurate with the responsibilities of the position. Adopt and apply all Merrick policies and procedures and apply them on assignments. Educate clients on pertinent regulations, consensus standards, manufacturers use instructions, and best practices concerning their laboratories, operations, safety programs, hazard control systems, biocontainment, equipment, hazardous materials storage, waste treatment and disposal processes, and all associated documents and records. REQUIRED QUALIFICATIONS Applicant must be a U.K. Citizen This position may require vaccination as mandated by client polices Applicants must be willing to travel up to 50% domestically and internationally as needed to support client projects Technical Master's degree or higher in a science related field from an accredited program. Minimum of five (5) years of experience in laboratory operations, biosafety, & biosecurity. Previous experience in high and maximum containment laboratories (CL/BSL 3 or higher) is required. Must have technical knowledge of regulatory requirements regarding biosafety, HSE, ACDP, SAPO, GMO, and IATA. Technical knowledge of consensus standards (e.g., ANSI, ASHRAE, British Standards, CIBSE, HTM, ISO) is preferred. Experience performing laboratory assessments for biological, chemical, and physical hazards for all laboratory containment levels for human, animal, and plant materials. General awareness of clinical laboratory operations and hazards associated with diagnostic, clinical microbiology, chemistry, blood bank, histopathology, and gross sectioning is preferred. General awareness of laboratory operations and hazards associated with academic laboratories (e.g., chemistry, biology, microbiology) is preferred Ability to coordinate the collection of data from laboratory assessments to determine gaps and needs to meet design requirements. Computer Skills: Microsoft Office (Word, Excel, PowerPoint, Project, etc.). Ability to work on multiple projects which includes resourcing, tracking, follow up and follow through to project completion. Well organized, detail oriented, and self motivated professional with strong verbal and written communication skills. Strong desire to work in a team environment. Flexibility/adaptability to work in a fast paced environment. DESIRED QUALIFICATIONS Credentialed biosafety professional Advanced degree in the life and/or biological sciences (M.S. or Ph.D.) Past support of a ACDP or SAPO regulated entity Environment of Care committee member or participant Clinical laboratory operations General environment of care surveillance Clinical risk assessment and management PERKS Employee Owned - all eligible U.S. employees have an Employee Stock Ownership Account. Robust Employee Referral Program. Annual performance and compensation reviews. Professional Training and Development. Employee Recognition Awards. Peer Mentor Program And Much More! ADDITIONAL INFORMATION Apply online only. No e mail, hard copy or third party resumes accepted. At Merrick, every resume is carefully reviewed by our team of experienced human recruiters-never by AI. We are committed to a fully human centered hiring process, ensuring each candidate receives thoughtful, personalized attention at every stage. Merrick & Company offers a competitive compensation and benefits package which includes health insurance, dental and vision coverage, 401(k), and paid time off (PTO). Merrick is an Equal Opportunity Employer, including disability/vets. Employment with Merrick is contingent upon completion of a pre employment background check, MVR check, and drug screen.
May 01, 2026
Full time
OVERVIEW Merrick & Company, an employee owned company, is seeking an experienced Senior Scientist in Biosafety and Laboratory Operations to join our growing team. The person would become a crucial part of a key Merrick growth initiative in Life Sciences, Biosafety & Biosecurity, and Laboratory Operations markets. This position is open for work in London, with ability to travel to client sites across the UK and Europe. The Scientist must be capable of coordinating and supporting a multi faced series of projects related to laboratory operations, operational planning, biosafety & biosecurity, regulatory compliance, and the integration of consensus standards (e.g., ANSI, ASHRAE), manufacturers use instructions, and industry best practices. This person would support the Science & Technology team with duties and coordination as part of a team of scientists, engineers, and subject matter experts. The position will work interactively with other teams responsible for laboratory design, commissioning, and operational planning, development of laboratory IT and IS systems, and development of laboratory programs (e.g., clinical, diagnostic, and research safety, bio risk management, small to large animal laboratory issues, etc.). This position requires the ability to not only be proficient in biosafety, but also clinical and research laboratory operations with an understanding of how laboratory activities, controls, and equipment function to support the containment and isolation of laboratory hazards. This person will support development of high level technical products and deliverables, problem solving and planning for high visibility projects, and as such must possess excellent communication skills. This position requires a high level of demonstrated effectiveness in working with HM government entities, regulators, and academic, clinical, and academic administrators, internal team members and outside consulting team members. The successful candidate will be required to interface with a broad spectrum of clients for Life Sciences projects located anywhere within the UK. Moderate travel (up to 50%) may be required. WHAT YOU'LL DO Provide strategy, development, execution, and technical knowledge for project deliverables related to laboratory operations, biological risk identification, assessment, characterization, management, exposure assessment and control, general safety, occupational hygiene, health and environmental management, animal care and use and regulatory compliance. Possess strong oral and written communications and interpersonal skills to effectively interface with clients and team members to: Ensure adherence to project quality of deliverables, products, and schedule Address issues related to the interface of laboratory operations, compliance, and operational planning Prepare complex studies, reports, plans, specifications, and other products for project deliverables. Support document preparation to aid clients in obtaining and maintaining regulatory registrations and permits. Support proposal development and marketing initiatives. Support leadership to ensure that project schedules and budgets are met and communicate with leadership any issues and concerns. Exercise initiative, judgment, and knowledge commensurate with the responsibilities of the position. Adopt and apply all Merrick policies and procedures and apply them on assignments. Educate clients on pertinent regulations, consensus standards, manufacturers use instructions, and best practices concerning their laboratories, operations, safety programs, hazard control systems, biocontainment, equipment, hazardous materials storage, waste treatment and disposal processes, and all associated documents and records. REQUIRED QUALIFICATIONS Applicant must be a U.K. Citizen This position may require vaccination as mandated by client polices Applicants must be willing to travel up to 50% domestically and internationally as needed to support client projects Technical Master's degree or higher in a science related field from an accredited program. Minimum of five (5) years of experience in laboratory operations, biosafety, & biosecurity. Previous experience in high and maximum containment laboratories (CL/BSL 3 or higher) is required. Must have technical knowledge of regulatory requirements regarding biosafety, HSE, ACDP, SAPO, GMO, and IATA. Technical knowledge of consensus standards (e.g., ANSI, ASHRAE, British Standards, CIBSE, HTM, ISO) is preferred. Experience performing laboratory assessments for biological, chemical, and physical hazards for all laboratory containment levels for human, animal, and plant materials. General awareness of clinical laboratory operations and hazards associated with diagnostic, clinical microbiology, chemistry, blood bank, histopathology, and gross sectioning is preferred. General awareness of laboratory operations and hazards associated with academic laboratories (e.g., chemistry, biology, microbiology) is preferred Ability to coordinate the collection of data from laboratory assessments to determine gaps and needs to meet design requirements. Computer Skills: Microsoft Office (Word, Excel, PowerPoint, Project, etc.). Ability to work on multiple projects which includes resourcing, tracking, follow up and follow through to project completion. Well organized, detail oriented, and self motivated professional with strong verbal and written communication skills. Strong desire to work in a team environment. Flexibility/adaptability to work in a fast paced environment. DESIRED QUALIFICATIONS Credentialed biosafety professional Advanced degree in the life and/or biological sciences (M.S. or Ph.D.) Past support of a ACDP or SAPO regulated entity Environment of Care committee member or participant Clinical laboratory operations General environment of care surveillance Clinical risk assessment and management PERKS Employee Owned - all eligible U.S. employees have an Employee Stock Ownership Account. Robust Employee Referral Program. Annual performance and compensation reviews. Professional Training and Development. Employee Recognition Awards. Peer Mentor Program And Much More! ADDITIONAL INFORMATION Apply online only. No e mail, hard copy or third party resumes accepted. At Merrick, every resume is carefully reviewed by our team of experienced human recruiters-never by AI. We are committed to a fully human centered hiring process, ensuring each candidate receives thoughtful, personalized attention at every stage. Merrick & Company offers a competitive compensation and benefits package which includes health insurance, dental and vision coverage, 401(k), and paid time off (PTO). Merrick is an Equal Opportunity Employer, including disability/vets. Employment with Merrick is contingent upon completion of a pre employment background check, MVR check, and drug screen.
Manufacturing Technician Location: Office based, Whiteley PO15 7AF Salary: £29,000-£33,000, depending on skills and experience Contract: Full Time, Permanent What we offer: In common with many start-ups, we offer a fast-paced, dynamic environment where you can learn a huge amount in a short time, with exposure to everything happening in the company. We look after our staff as they are our key asset, and offer regular salary reviews, share options, lots of flexibility and generous training allowances. Our facilities are commutable from most of Hampshire, West Sussex, Poole, Bournemouth etc. About the company: iFAST is an innovative new medical technology spinout from the University of Southampton, led by an experienced team of entrepreneurs and scientists. We have developed a game changing microfluidics based test for antimicrobial susceptibility, reducing the test time from 48+ to 3 hours to help combat the global threat of antimicrobial resistance, which kills more than 1 million people per year. Job Role: We are now seeking a manufacturing technician to join our team in Whiteley, Hampshire, reporting to our Head of Manufacturing Operations, to help us build our instruments and manufacture our microfluidic chips to bring our technology to market. Responsibilities: Manufacturing: • Manufacturing of microfluidic chips and iFAST instruments in accordance with written instructions • Perform complex, detailed operations on small parts, working under a microscope where necessary • Keep accurate, clear manufacturing records and maintain clean, organised work area • Comply with work instructions, guidelines and regulatory requirements • Report problems (and potential problems) with quality, processes, equipment and materials to management • Ensure all equipment used is appropriately cleaned, maintained, calibrated before use Design & Development: • Assist with product development by assembling prototype devices and providing feedback • Perform product testing to provide information on product performance • Keep accurate, clear and complete records for inclusion within the Design History File • Writing new work instructions and process flow cards Quality System: • Work within medical device quality system in accordance with EN ISO 13485:2016 and 21 CFR 820 • Responsible for operating and maintaining the manufacturing laboratory equipment as specified by the relevant SOPs • Input into product quality meetings, offer ideas and corrective actions Support: • Provide technical support to Quality (e.g. training, input into non-conformance investigations, customer complaints) • Assist with documentation in accordance with standards, manufacturing procedure documentation, and SOPs. • Provide feedback and support for continuous improvement projects • Periodically presenting your work to the team and our collaborators, and performing other tasks as assigned Knowledge, Skills & Experience: • Good numeracy and basic IT skills; ability to work in accordance with documented work instructions • Appropriate engineering or medical devices experience working to ISO 13485 or GLP • Excellent practical skills with experience using precision manufacturing equipment • Experience of working within a controlled environment, such as a GLP laboratory or cleanroom • Familiarity with wiring, cable harnesses, crimping and soldering is desirable but not essential • The ability to work well in a team and to manage & prioritize your own workload with minimal supervision • Great interpersonal skills, as we are a small, close-knit team with a culture of togetherness • Good problem-solving skills and the ability to use your initiative to fix things when they go wrong • An accurate and methodical approach to work, including documentation in compliant with our QMS • Being a self-starter you should have great self-motivation to do a great job and to help the company succeed • Excellent attention to detail including reading CAD drawings If you feel you have the necessary skills and experience to be successful in this role, click on APPLY today, forwarding an up-to-date copy of your CV for consideration in the first instance. No agencies please.
May 01, 2026
Full time
Manufacturing Technician Location: Office based, Whiteley PO15 7AF Salary: £29,000-£33,000, depending on skills and experience Contract: Full Time, Permanent What we offer: In common with many start-ups, we offer a fast-paced, dynamic environment where you can learn a huge amount in a short time, with exposure to everything happening in the company. We look after our staff as they are our key asset, and offer regular salary reviews, share options, lots of flexibility and generous training allowances. Our facilities are commutable from most of Hampshire, West Sussex, Poole, Bournemouth etc. About the company: iFAST is an innovative new medical technology spinout from the University of Southampton, led by an experienced team of entrepreneurs and scientists. We have developed a game changing microfluidics based test for antimicrobial susceptibility, reducing the test time from 48+ to 3 hours to help combat the global threat of antimicrobial resistance, which kills more than 1 million people per year. Job Role: We are now seeking a manufacturing technician to join our team in Whiteley, Hampshire, reporting to our Head of Manufacturing Operations, to help us build our instruments and manufacture our microfluidic chips to bring our technology to market. Responsibilities: Manufacturing: • Manufacturing of microfluidic chips and iFAST instruments in accordance with written instructions • Perform complex, detailed operations on small parts, working under a microscope where necessary • Keep accurate, clear manufacturing records and maintain clean, organised work area • Comply with work instructions, guidelines and regulatory requirements • Report problems (and potential problems) with quality, processes, equipment and materials to management • Ensure all equipment used is appropriately cleaned, maintained, calibrated before use Design & Development: • Assist with product development by assembling prototype devices and providing feedback • Perform product testing to provide information on product performance • Keep accurate, clear and complete records for inclusion within the Design History File • Writing new work instructions and process flow cards Quality System: • Work within medical device quality system in accordance with EN ISO 13485:2016 and 21 CFR 820 • Responsible for operating and maintaining the manufacturing laboratory equipment as specified by the relevant SOPs • Input into product quality meetings, offer ideas and corrective actions Support: • Provide technical support to Quality (e.g. training, input into non-conformance investigations, customer complaints) • Assist with documentation in accordance with standards, manufacturing procedure documentation, and SOPs. • Provide feedback and support for continuous improvement projects • Periodically presenting your work to the team and our collaborators, and performing other tasks as assigned Knowledge, Skills & Experience: • Good numeracy and basic IT skills; ability to work in accordance with documented work instructions • Appropriate engineering or medical devices experience working to ISO 13485 or GLP • Excellent practical skills with experience using precision manufacturing equipment • Experience of working within a controlled environment, such as a GLP laboratory or cleanroom • Familiarity with wiring, cable harnesses, crimping and soldering is desirable but not essential • The ability to work well in a team and to manage & prioritize your own workload with minimal supervision • Great interpersonal skills, as we are a small, close-knit team with a culture of togetherness • Good problem-solving skills and the ability to use your initiative to fix things when they go wrong • An accurate and methodical approach to work, including documentation in compliant with our QMS • Being a self-starter you should have great self-motivation to do a great job and to help the company succeed • Excellent attention to detail including reading CAD drawings If you feel you have the necessary skills and experience to be successful in this role, click on APPLY today, forwarding an up-to-date copy of your CV for consideration in the first instance. No agencies please.
£30,000.00 to £34,000.00 per year, +Benefits Contract Type: Permanent Hours: Full time Disability Confident: No Closing Date: 26/04/2026 About this job Title: Research Technician Location: South Wales Salary: Up to £34,000 depending on experience Term: Permanent Benefits: enhanced training and development opportunities, flexible start and finish times, half day finish on a Friday. SRG is exclusively partnered with a leading manufacturer of personal care and beauty products in South Wales. As the company continues to grow, they are looking to add a Research Technician to their Innovation team. They are known for their supportive, collaborative culture and are recognised as industry leaders, with consumer health and wellbeing at the heart of what they do. This role would suit candidates who have 2 years of experience in a fast paced laboratory, formulation, analytical testing or research environments. Graduates will also be considered but they must have already graduated from university. Working Hours: Monday to Friday, 37.5 hours a week, 25 days holiday + 8 bank holidays. Supporting day-to-day laboratory activities, ensuring safe, compliant, and efficient working practices; working alongside Contribute to hands on R&D projects, supporting the development and optimisation of innovative skin and hair care formulations; Conduct wet chemistry testing and analytical testing on innovation projects using pH, Density, Viscosity, titrations, Stability testing, UV-Vis, microscopy, spectroscopy, chromatography (LC) and so on; Assist with the coordination and execution of experimental projects, preparing laboratory equipment and materials while maintaining accurate data records; Carrying out formulation compatibility and characterisation testing; Working closely with senior researchers and cross functional teams on skincare and haircare innovation projects Requirements A degree (BSc, MSc OR PhD) in Pharmaceutical Sciences, Chemistry, Cosmetic Science or Pharmaceutical and Cosmetic Science must have already graduated / finished uni. Must have 2 years' recent experience in a laboratory environment Full right to work in the UK there is no sponsorship available for this role 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 would like to apply for this position, please use the link provided. Alternatively, please email a copy of your CV. For more information regarding this position or any others, please call Rhi on . If you have a scientific background and this position is not relevant / suitable for you, please feel free to get in touch or visit to view our other vacancies. The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.
May 01, 2026
Full time
£30,000.00 to £34,000.00 per year, +Benefits Contract Type: Permanent Hours: Full time Disability Confident: No Closing Date: 26/04/2026 About this job Title: Research Technician Location: South Wales Salary: Up to £34,000 depending on experience Term: Permanent Benefits: enhanced training and development opportunities, flexible start and finish times, half day finish on a Friday. SRG is exclusively partnered with a leading manufacturer of personal care and beauty products in South Wales. As the company continues to grow, they are looking to add a Research Technician to their Innovation team. They are known for their supportive, collaborative culture and are recognised as industry leaders, with consumer health and wellbeing at the heart of what they do. This role would suit candidates who have 2 years of experience in a fast paced laboratory, formulation, analytical testing or research environments. Graduates will also be considered but they must have already graduated from university. Working Hours: Monday to Friday, 37.5 hours a week, 25 days holiday + 8 bank holidays. Supporting day-to-day laboratory activities, ensuring safe, compliant, and efficient working practices; working alongside Contribute to hands on R&D projects, supporting the development and optimisation of innovative skin and hair care formulations; Conduct wet chemistry testing and analytical testing on innovation projects using pH, Density, Viscosity, titrations, Stability testing, UV-Vis, microscopy, spectroscopy, chromatography (LC) and so on; Assist with the coordination and execution of experimental projects, preparing laboratory equipment and materials while maintaining accurate data records; Carrying out formulation compatibility and characterisation testing; Working closely with senior researchers and cross functional teams on skincare and haircare innovation projects Requirements A degree (BSc, MSc OR PhD) in Pharmaceutical Sciences, Chemistry, Cosmetic Science or Pharmaceutical and Cosmetic Science must have already graduated / finished uni. Must have 2 years' recent experience in a laboratory environment Full right to work in the UK there is no sponsorship available for this role 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 would like to apply for this position, please use the link provided. Alternatively, please email a copy of your CV. For more information regarding this position or any others, please call Rhi on . If you have a scientific background and this position is not relevant / suitable for you, please feel free to get in touch or visit to view our other vacancies. The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy.
Join Lucideon as a Development Scientist - Biosciences! About Us Lucideon is a globally recognised materials and technology development organisation, working with clients across biotechnology, pharmaceuticals, advanced therapies and other high growth life sciences sectors. We combine deep scientific expertise with a collaborative, client focused approach to help organisations solve complex technical challenges in regulated environments. As our biosciences capability continues to grow, we are looking for a Development Scientist - Biosciences to play a key role in delivering high quality laboratory projects and supporting the ongoing development of our Biology offering. Purpose of the Role The Biology Project Scientist will support the growth of Lucideon's Biosciences capability from an emerging offering into a broad, robust service that meets the needs of biotechnology, pharmaceutical and advanced therapy markets. This role is primarily focused on the delivery of Cell Biology projects, including the design, execution and reporting of cell based studies. You will also contribute to a wider range of bioscience activities such as microbiology projects, cleaning and sterilisation programmes, and cross team technical initiatives. This is an excellent opportunity for a technically strong biologist who enjoys hands on laboratory work, thrives in regulated environments and wants to help shape and mature a growing scientific capability. Key Responsibilities Project Delivery Deliver discrete laboratory programmes of work for Lucideon's customers, ensuring high technical and scientific standards throughout. Apply best practice technical methods and project delivery principles to meet or exceed on time delivery KPIs. Develop, write and implement new methods or protocols tailored to specific project requirements. Act as a role model for Good Laboratory Practice (GLP), hygiene and safe working practices across all laboratory spaces. Work collaboratively with technical, commercial and project teams to ensure projects are clearly scoped and successfully delivered. Provide technical expertise and delivery support to other teams within Lucideon's Advanced & Engineering (A&E) department when required. Quality & Compliance Ensure strict adherence to client confidentiality, cGMP and all applicable quality standards at all times. Follow and comply with Lucideon's Quality Management System, processes and protocols. Provide additional laboratory and quality support to the wider organisation as needed. Client Interaction & Technical Scoping Support the Sales team during customer calls to help uncover and shape technical requirements. Contribute to the development and scoping of biology based solutions. Provide credible technical input into proposals and Statements of Work. Support the creation of case studies, technical materials and marketing content aligned with biology services. About You Qualifications Bachelor's degree (minimum) in Biological Sciences or a related discipline. Experience Strong hands on experience working within cell biology laboratories. Practical experience in microbiology or microbial handling is highly desirable. Experience working in a regulated laboratory environment (e.g. GMP, GLP) is preferred. Experience within the Life Sciences sector is advantageous. Skills & Attributes Technically credible biologist, able to translate customer requirements into practical laboratory solutions. Detail oriented with a strong commitment to quality, compliance and documentation. Curious, inquisitive and solution focused, with a willingness to develop new skills and capabilities. A natural collaborator who enjoys working across multidisciplinary teams. Confident self starter, comfortable taking ownership of work and driving projects forward. Excellent organisational skills with the ability to prioritise a varied workload. Strong written and verbal communication skills. Based within reasonable commuting distance of Stone, Staffordshire. Core Features & Benefits Permanent position Onsite role at our Stone, Staffordshire facility 37 hours per week, Monday-Friday Private Medical Insurance Medical Cash Plan 25 days annual leave + bank holidays (including Christmas shutdown) Pension scheme matched up to 5% Life Assurance up to 4 basic salary Ready to Grow Your Cell Biology Career? If you are a hands on cell biologist looking to apply your skills in a collaborative, regulated, project driven environment - and want to be part of a growing biosciences capability - we would love to hear from you. Apply now and join Lucideon as a Development Scientist - Biosciences
May 01, 2026
Full time
Join Lucideon as a Development Scientist - Biosciences! About Us Lucideon is a globally recognised materials and technology development organisation, working with clients across biotechnology, pharmaceuticals, advanced therapies and other high growth life sciences sectors. We combine deep scientific expertise with a collaborative, client focused approach to help organisations solve complex technical challenges in regulated environments. As our biosciences capability continues to grow, we are looking for a Development Scientist - Biosciences to play a key role in delivering high quality laboratory projects and supporting the ongoing development of our Biology offering. Purpose of the Role The Biology Project Scientist will support the growth of Lucideon's Biosciences capability from an emerging offering into a broad, robust service that meets the needs of biotechnology, pharmaceutical and advanced therapy markets. This role is primarily focused on the delivery of Cell Biology projects, including the design, execution and reporting of cell based studies. You will also contribute to a wider range of bioscience activities such as microbiology projects, cleaning and sterilisation programmes, and cross team technical initiatives. This is an excellent opportunity for a technically strong biologist who enjoys hands on laboratory work, thrives in regulated environments and wants to help shape and mature a growing scientific capability. Key Responsibilities Project Delivery Deliver discrete laboratory programmes of work for Lucideon's customers, ensuring high technical and scientific standards throughout. Apply best practice technical methods and project delivery principles to meet or exceed on time delivery KPIs. Develop, write and implement new methods or protocols tailored to specific project requirements. Act as a role model for Good Laboratory Practice (GLP), hygiene and safe working practices across all laboratory spaces. Work collaboratively with technical, commercial and project teams to ensure projects are clearly scoped and successfully delivered. Provide technical expertise and delivery support to other teams within Lucideon's Advanced & Engineering (A&E) department when required. Quality & Compliance Ensure strict adherence to client confidentiality, cGMP and all applicable quality standards at all times. Follow and comply with Lucideon's Quality Management System, processes and protocols. Provide additional laboratory and quality support to the wider organisation as needed. Client Interaction & Technical Scoping Support the Sales team during customer calls to help uncover and shape technical requirements. Contribute to the development and scoping of biology based solutions. Provide credible technical input into proposals and Statements of Work. Support the creation of case studies, technical materials and marketing content aligned with biology services. About You Qualifications Bachelor's degree (minimum) in Biological Sciences or a related discipline. Experience Strong hands on experience working within cell biology laboratories. Practical experience in microbiology or microbial handling is highly desirable. Experience working in a regulated laboratory environment (e.g. GMP, GLP) is preferred. Experience within the Life Sciences sector is advantageous. Skills & Attributes Technically credible biologist, able to translate customer requirements into practical laboratory solutions. Detail oriented with a strong commitment to quality, compliance and documentation. Curious, inquisitive and solution focused, with a willingness to develop new skills and capabilities. A natural collaborator who enjoys working across multidisciplinary teams. Confident self starter, comfortable taking ownership of work and driving projects forward. Excellent organisational skills with the ability to prioritise a varied workload. Strong written and verbal communication skills. Based within reasonable commuting distance of Stone, Staffordshire. Core Features & Benefits Permanent position Onsite role at our Stone, Staffordshire facility 37 hours per week, Monday-Friday Private Medical Insurance Medical Cash Plan 25 days annual leave + bank holidays (including Christmas shutdown) Pension scheme matched up to 5% Life Assurance up to 4 basic salary Ready to Grow Your Cell Biology Career? If you are a hands on cell biologist looking to apply your skills in a collaborative, regulated, project driven environment - and want to be part of a growing biosciences capability - we would love to hear from you. Apply now and join Lucideon as a Development Scientist - Biosciences
Team Leader, Pilot Plant Support and Analytical Equipment Validation We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme. We embrace modern work practices; our Performance with Choice programme offers a hybrid working model, empowering you to find the optimal balance between remote and in-office work. You will lead a team of analytical scientists and analytical equipment validation specialists to deliver validated analytical equipment and high-quality analytical data to support discovery and development across multiple projects. You will work closely with cross functional colleagues to develop and implement analytical strategies. We value clear thinkers who coach others, solve practical problems, and drive continuous improvement. This role offers growth, meaning, and the chance to apply science and technology to help get ahead of disease together. Responsibilities Lead and supervise a team of analytical scientists and specialists, ensuring effective team performance, development to build capability / resilience and succession planning. Approve analytical test results for release or rejection of products, excipients, packaging components and purified water, ensuring compliance with GMP, corporate policies and standards to ensure patient safety, product quality and data integrity. Where appropriate prepare, review, and approve regulatory modules to support drug progression into clinical trials and global markets. Provide technical leadership in developing, validating, and transferring analytical methods for comparator testing, release testing, and cleaning verification. Ensure computerized laboratory analytical equipment and systems used to support regulatory submissions to develop, test or manufacture materials within DDS, are qualified or validated as appropriate and maintained in an appropriately validated state in accordance with the relevant regulations, corporate policies and standards to ensure patient safety, product quality and data integrity. Establish and maintain partnerships with clinical manufacturing, product development teams, and external collaborators for efficient service delivery. Able to apply digital tools to drive continuous improvement and deliver simplified, efficient business processes. Basic Qualifications & Skills Degree in chemistry, analytical chemistry, pharmaceutical sciences or a related discipline, or equivalent practical experience. Demonstrated experience leading or supervising analytical scientists or analytical equipment specialists in an R&D or industrial laboratory environment. Strong hands on experience in chromatographic and dissolution techniques. Experience in analytical method development, qualification and validation for release and stability testing. Proven ability to work in a matrix environment and collaborate with cross functional teams. Clear written and verbal communication skills and experience preparing technical reports and regulatory documentation. Preferred Qualifications & Skills Advanced degree (MSc or PhD) in a relevant discipline or equivalent experience. Experience with method transfer to manufacturing sites or external partners. Knowledge of regulatory frameworks and expectations for analytical data (e.g., ICH guidelines, ISO standards). Experience with emerging analytical technologies, automation and application of digital tools. Background in small molecule analytical development. Track record of mentoring scientists and building team capability. Closing Date for Applications - 26th April 2026 GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law. If you require adjustments to our process to demonstrate your strengths and capabilities, contact .
May 01, 2026
Full time
Team Leader, Pilot Plant Support and Analytical Equipment Validation We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme. We embrace modern work practices; our Performance with Choice programme offers a hybrid working model, empowering you to find the optimal balance between remote and in-office work. You will lead a team of analytical scientists and analytical equipment validation specialists to deliver validated analytical equipment and high-quality analytical data to support discovery and development across multiple projects. You will work closely with cross functional colleagues to develop and implement analytical strategies. We value clear thinkers who coach others, solve practical problems, and drive continuous improvement. This role offers growth, meaning, and the chance to apply science and technology to help get ahead of disease together. Responsibilities Lead and supervise a team of analytical scientists and specialists, ensuring effective team performance, development to build capability / resilience and succession planning. Approve analytical test results for release or rejection of products, excipients, packaging components and purified water, ensuring compliance with GMP, corporate policies and standards to ensure patient safety, product quality and data integrity. Where appropriate prepare, review, and approve regulatory modules to support drug progression into clinical trials and global markets. Provide technical leadership in developing, validating, and transferring analytical methods for comparator testing, release testing, and cleaning verification. Ensure computerized laboratory analytical equipment and systems used to support regulatory submissions to develop, test or manufacture materials within DDS, are qualified or validated as appropriate and maintained in an appropriately validated state in accordance with the relevant regulations, corporate policies and standards to ensure patient safety, product quality and data integrity. Establish and maintain partnerships with clinical manufacturing, product development teams, and external collaborators for efficient service delivery. Able to apply digital tools to drive continuous improvement and deliver simplified, efficient business processes. Basic Qualifications & Skills Degree in chemistry, analytical chemistry, pharmaceutical sciences or a related discipline, or equivalent practical experience. Demonstrated experience leading or supervising analytical scientists or analytical equipment specialists in an R&D or industrial laboratory environment. Strong hands on experience in chromatographic and dissolution techniques. Experience in analytical method development, qualification and validation for release and stability testing. Proven ability to work in a matrix environment and collaborate with cross functional teams. Clear written and verbal communication skills and experience preparing technical reports and regulatory documentation. Preferred Qualifications & Skills Advanced degree (MSc or PhD) in a relevant discipline or equivalent experience. Experience with method transfer to manufacturing sites or external partners. Knowledge of regulatory frameworks and expectations for analytical data (e.g., ICH guidelines, ISO standards). Experience with emerging analytical technologies, automation and application of digital tools. Background in small molecule analytical development. Track record of mentoring scientists and building team capability. Closing Date for Applications - 26th April 2026 GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law. If you require adjustments to our process to demonstrate your strengths and capabilities, contact .
A leading materials science company in the UK is expanding and hiring Materials Scientists with ceramics expertise. This is an opportunity to join a world-class organization and work at one of Europe's most advanced centers for Advanced Ceramics. Candidates should have experience in applications of advanced materials, technical team leadership, and research into new applications. The position offers meaningful work and benefits such as private medical insurance for all colleagues.
May 01, 2026
Full time
A leading materials science company in the UK is expanding and hiring Materials Scientists with ceramics expertise. This is an opportunity to join a world-class organization and work at one of Europe's most advanced centers for Advanced Ceramics. Candidates should have experience in applications of advanced materials, technical team leadership, and research into new applications. The position offers meaningful work and benefits such as private medical insurance for all colleagues.
Analytical & Materials Scientist Location: Viatris, Sandwich, UK Company: Synergy Department: Analytical Control & Development Employment Type: Full-Time About the Role Viatris is seeking an Analytical & Materials Scientist to join our Analytical Control & Development team in Sandwich click apply for full job details
May 01, 2026
Full time
Analytical & Materials Scientist Location: Viatris, Sandwich, UK Company: Synergy Department: Analytical Control & Development Employment Type: Full-Time About the Role Viatris is seeking an Analytical & Materials Scientist to join our Analytical Control & Development team in Sandwich click apply for full job details
About Spotfire Spotfire is a business unit of Cloud Software Group, one of the largest enterprise software companies in the world. Spotfire combines visualizations and advanced analytics to allow experts in their field to find industry-specific solutions the human mind or computers can't solve alone. Our more than 10,000 customers include: Majority of the top 10 Energy companies in the world Majority of the top 10 Life Sciences companies in the world 7 of the world's top 10 Manufacturing companies Several other major companies in banking, retail, and airlines We are looking for people with a passion to make a big difference by doing the job they love - dynamic individuals willing to take the risks necessary to make big ideas come to life and who are comfortable collaborating in our creative, innovation-driven environment. Overview Our Customer Success team is central to our global strategy. Their work enables our clients to quickly create and deploy solutions that drive innovation, optimise operations, offer insight, and drive transformation. Ultimately the team is responsible for enabling our client's competitiveness by accelerating ROI from any data science initiative with products that transform data into insight. Operating across sectors and with a high degree of independence, our data scientists have helped improve performance for F1 teams, improved energy production reliability through advanced statistical modeling, and enhanced product quality and optimized yield by detecting defects, forecasting production issues, and optimizing resource allocation to improve efficiency. We are looking for a Data Scientist to join our team. You are seeking an opportunity to challenge and develop both your knowledge as well as our client's data science capabilities. You will join a team of highly collaborative individuals and will play a key role in developing our capability and establishing Spotfire leadership in the industrial analytics space. Through the content you create and deliver, you will be enabling our partners and customers on their Spotfire skills and will draw together our Spotfire user community. The role is based in the United Kingdom as a remote role. We are open to considering other European locations as well. Responsibilities The job holder will be expected to contribute to the following with varying degrees of priority: Work with customers and partners to understand their education needs for Spotfire, Spotfire Statistica, and Spotfire Data Virtualization. Lead development and maintenance of education content, including online courses and certification materials, for Spotfire, Spotfire Statistica, and Spotfire Data Virtualization. Content will need to be accurate, relevant, and aligned with industry standards. Collaborate with others in the Spotfire Education and Community team to create Dr. Spotfire webinars and Quick Tip videos Manage relationships with IT and external vendors for required software tools. Incorporate feedback from customers and internal staff to improve the effectiveness of educational content and initiatives. Contribute Spotfire learning materials to and Spotfire community. Moderate Spotfire community as it relates to Spotfire enablement. Increase awareness and enable adoption of Spotfire Industry Pro through Spotfire community content creation. Represent the Spotfire team as an instructor in industry events and external conferences. Qualifications 3+ years of experience in data analytics and delivery of demonstrations, projects, engagements, or deployed software applications involving predictive analytics such as machine learning. Ability to understand data and data goals, and find solutions that are appropriate to the task. Exceptional presentation and public speaking skills, with demonstrated experience instructing/training technical concepts to diverse audiences (customers, partners, and at industry events). 3+ years of experience with Python or R, and working knowledge of SQL. Experience with a variety of data science tools, including data visualization platforms (e.g., Spotfire, Tableau) and predictive modeling environments (e.g., KNIME, Matlab). Deep, hands on experience with Spotfire, Spotfire Statistica, and/or Spotfire Data Virtualization is highly desired. Familiarity with Cloud ML platforms (e.g., AzureML, GCP), Big Data tools (e.g., Databricks, Spark, Snowflake), or enterprise data preparation/integration tools (e.g., Data Virtualization, Java, .Net) a plus. A degree in Computer Science, Statistics, Data Science or related analytical field of study, with graduate classes in statistics and data mining. Demonstrated ability to design, develop and maintain technical educational content, including online courses, documentation and video tutorials. Language skills: Business level English; other languages are a plus. Experience moderating and engaging with a technical user community, or proven ability to drive adoption and awareness through content creation (blogs, social media, forums) Please note you must have full working rights for the country you are applying for. If on a work permit or visa, please make sure the details along with expiry date are included on your application About Us: Cloud Software Group is one of the world's largest cloud solution providers, serving more than 100 million users around the globe. When you join Cloud Software Group, you are making a difference for real people, each of whom count on our suite of cloud-based products to get work done - from anywhere. Members of our team will tell you that we value passion for technology and the courage to take risks. Everyone is empowered to learn, dream, and build the future of work. We are on the brink of another Cambrian leap - a moment of immense evolution and growth. And we need your expertise and experience to do it. Now is the perfect time to move your skills to the cloud. Cloud Software Group is firmly committed to Equal Employment Opportunity (EEO) and to compliance with all federal, state and local laws that prohibit employment discrimination. All qualified applicants will receive consideration for employment without regard to age, race, color, creed, sex or gender, sexual orientation, gender identity, gender expression, ethnicity, national origin, ancestry, citizenship, religion, genetic carrier status, disability, pregnancy, childbirth or related medical conditions (including lactation status), marital status, military service, protected veteran status, political activity or affiliation, taking or requesting statutorily protected leave and other protected classifications. If you need a reasonable accommodation due to a disability during any part of the application process, please contact us via Bridge portal for assistance.
Apr 30, 2026
Full time
About Spotfire Spotfire is a business unit of Cloud Software Group, one of the largest enterprise software companies in the world. Spotfire combines visualizations and advanced analytics to allow experts in their field to find industry-specific solutions the human mind or computers can't solve alone. Our more than 10,000 customers include: Majority of the top 10 Energy companies in the world Majority of the top 10 Life Sciences companies in the world 7 of the world's top 10 Manufacturing companies Several other major companies in banking, retail, and airlines We are looking for people with a passion to make a big difference by doing the job they love - dynamic individuals willing to take the risks necessary to make big ideas come to life and who are comfortable collaborating in our creative, innovation-driven environment. Overview Our Customer Success team is central to our global strategy. Their work enables our clients to quickly create and deploy solutions that drive innovation, optimise operations, offer insight, and drive transformation. Ultimately the team is responsible for enabling our client's competitiveness by accelerating ROI from any data science initiative with products that transform data into insight. Operating across sectors and with a high degree of independence, our data scientists have helped improve performance for F1 teams, improved energy production reliability through advanced statistical modeling, and enhanced product quality and optimized yield by detecting defects, forecasting production issues, and optimizing resource allocation to improve efficiency. We are looking for a Data Scientist to join our team. You are seeking an opportunity to challenge and develop both your knowledge as well as our client's data science capabilities. You will join a team of highly collaborative individuals and will play a key role in developing our capability and establishing Spotfire leadership in the industrial analytics space. Through the content you create and deliver, you will be enabling our partners and customers on their Spotfire skills and will draw together our Spotfire user community. The role is based in the United Kingdom as a remote role. We are open to considering other European locations as well. Responsibilities The job holder will be expected to contribute to the following with varying degrees of priority: Work with customers and partners to understand their education needs for Spotfire, Spotfire Statistica, and Spotfire Data Virtualization. Lead development and maintenance of education content, including online courses and certification materials, for Spotfire, Spotfire Statistica, and Spotfire Data Virtualization. Content will need to be accurate, relevant, and aligned with industry standards. Collaborate with others in the Spotfire Education and Community team to create Dr. Spotfire webinars and Quick Tip videos Manage relationships with IT and external vendors for required software tools. Incorporate feedback from customers and internal staff to improve the effectiveness of educational content and initiatives. Contribute Spotfire learning materials to and Spotfire community. Moderate Spotfire community as it relates to Spotfire enablement. Increase awareness and enable adoption of Spotfire Industry Pro through Spotfire community content creation. Represent the Spotfire team as an instructor in industry events and external conferences. Qualifications 3+ years of experience in data analytics and delivery of demonstrations, projects, engagements, or deployed software applications involving predictive analytics such as machine learning. Ability to understand data and data goals, and find solutions that are appropriate to the task. Exceptional presentation and public speaking skills, with demonstrated experience instructing/training technical concepts to diverse audiences (customers, partners, and at industry events). 3+ years of experience with Python or R, and working knowledge of SQL. Experience with a variety of data science tools, including data visualization platforms (e.g., Spotfire, Tableau) and predictive modeling environments (e.g., KNIME, Matlab). Deep, hands on experience with Spotfire, Spotfire Statistica, and/or Spotfire Data Virtualization is highly desired. Familiarity with Cloud ML platforms (e.g., AzureML, GCP), Big Data tools (e.g., Databricks, Spark, Snowflake), or enterprise data preparation/integration tools (e.g., Data Virtualization, Java, .Net) a plus. A degree in Computer Science, Statistics, Data Science or related analytical field of study, with graduate classes in statistics and data mining. Demonstrated ability to design, develop and maintain technical educational content, including online courses, documentation and video tutorials. Language skills: Business level English; other languages are a plus. Experience moderating and engaging with a technical user community, or proven ability to drive adoption and awareness through content creation (blogs, social media, forums) Please note you must have full working rights for the country you are applying for. If on a work permit or visa, please make sure the details along with expiry date are included on your application About Us: Cloud Software Group is one of the world's largest cloud solution providers, serving more than 100 million users around the globe. When you join Cloud Software Group, you are making a difference for real people, each of whom count on our suite of cloud-based products to get work done - from anywhere. Members of our team will tell you that we value passion for technology and the courage to take risks. Everyone is empowered to learn, dream, and build the future of work. We are on the brink of another Cambrian leap - a moment of immense evolution and growth. And we need your expertise and experience to do it. Now is the perfect time to move your skills to the cloud. Cloud Software Group is firmly committed to Equal Employment Opportunity (EEO) and to compliance with all federal, state and local laws that prohibit employment discrimination. All qualified applicants will receive consideration for employment without regard to age, race, color, creed, sex or gender, sexual orientation, gender identity, gender expression, ethnicity, national origin, ancestry, citizenship, religion, genetic carrier status, disability, pregnancy, childbirth or related medical conditions (including lactation status), marital status, military service, protected veteran status, political activity or affiliation, taking or requesting statutorily protected leave and other protected classifications. If you need a reasonable accommodation due to a disability during any part of the application process, please contact us via Bridge portal for assistance.
Market Access Medical Writer (Consultant) Location - London or Winchester with hybrid working as per departmental requirements (currently a MINIMUM of 40% (2 days per week) with Tuesday as the team day. In 2020 LCP launched our Heath Analytics practice, providing analytical and research services for organisations across the life sciences and healthcare industries. Our team brings together health economists, statisticians, market access specialists, epidemiologists, clinicians, and health data scientists alongside our established actuarial, analytics and technology teams to deliver new solutions for the fundamental challenges in health. Our team's mission is to help move health systems from importers of illness to exporters of health and to support our clients to deliver value to patients. This is underpinned by our approach to support clients to improve the population's health and reduce inequalities. What's the role? LCP's Health Analytics team works across the healthcare and life sciences markets, combining health expertise with innovative approaches from our work in other sectors to tackle leading health issues. Examples of the types of projects that this role would cover, include, but are not limited to: Development of GVDs and other similar documents i.e. early value dossiers, AMCP and other formulary access tools (including payer value decks, US Pre-approval information exchange materials, and HEOR/ access toolkits), payer value propositions/ messages and objection handlers Supporting HTA dossier development JCA submission dossier development Literature review and statistical analysis reports Publications including posters, abstracts and manuscripts Development of data visualisation/ infographic type deliverables Conference, advisory board and other similar reports Providing strategic recommendations on global clinical trial design to enable HTA and reimbursement success Identifying optimal routes for access in different markets Landscape assessment, including but not limited to, competitor, pricing and reimbursement and HTA Patient journey mapping Secondary and primary research to validate market access strategies Payer evidence needs and gap analysis To support our continued growth, we are looking for an experienced Consultant with a proven track record in medical writing, particularly as applied to market access deliverables, to join our team and play a key role in growing our market access and value communication offerings. You'll have experience in writing and managing the development of a wide variety of market access/ value communication deliverables, including but not limited to, Global Value Dossiers (GVDs), American Managed Care Pharmacy (AMCP) dossiers, other payer formulary packs, payer value decks, HTA submissions, value driver identification and value story development, objection handlers, white papers, data visualisation tools, medical education, real world study reports, SLR reports, training materials, and market access/ HEOR/ RWE focused manuscripts. If you are looking to make a tangible impact, help develop a sub-service with an established service area (including team training and development of processes and editorial standards), take on leadership opportunities, and grow your expertise in a supportive and dynamic environment, then this is the role for you! Your key responsibilities will be to: Act as lead writer in the delivery of high-quality content which is fully referenced and reflective of the evidence base, and which is tailored to the target audience in terms of its content and style Lead market access focused projects including those that have a significant medical writing component. This will include coordination and project management of internal delivery teams alongside client-facing coordination of projects Develop Health Analytics team "house style" and similar editorial standards, processes and templates, while also being responsible for reviewing the work of other members of the team and contributing to team training and development of internal resources tools and processes People responsibilities including the line management and development of junior members of the team, depending on candidate's experience and interests Conduct targeted secondary research utilising a wide variety of sources to address specific research questions i.e., understand disease and competitor landscape, current treatment pathways, pricing and reimbursement processes, payer value drivers etc. Support the conduct of qualitative and quantitative payer research and analysis to identify opportunities and challenges for client products in various healthcare markets. This may include leading on the design of surveys, conducting 1:1 in-depth interviews, advisory boards, roundtable and other primary research methodologies Develop value messages, dossiers, and other related payer value communication materials e.g. payer value decks, toolkits, objection handlers and internal training materials Support the preparation of client-facing presentations and reports, effectively communicating complex concepts to diverse audiences. Manage projects (administrative and financial) including acting as the day-to-day client contact on projects, while also tracking and closely managing project budgets to ensure profitable and timely delivery Contribute to thought leadership, business development and marketing activities What skills, qualities and experience are we looking for? Essential Demonstrable experience as a market access medical writer in a consultancy environment, to include preparing market access and HEOR focused medical writing projects (including but not limited to; GVDs, HTA dossiers, early value dossiers, AMCP and other formulary access tools, manuscripts, conference presentations, payer value propositions/ messages and objection handlers)A 2:1 degree or better plus a science/ health-related postgraduate qualification (Masters or PhD) in a life-science focused subject or in an English language focused subject, with proven experience of application in the healthcare market access arenaDemonstrable experience of working in MS PowerPoint and prose-based, MS Word and similar formats is required.Confidence in leading the preparation of client-facing presentations and reports, effectively communicating complex concepts to diverse audiencesAbility to conduct and guide others in targeted secondary research utilising a wide variety of sources to address specific research questions. In addition, you should have a s
Apr 30, 2026
Full time
Market Access Medical Writer (Consultant) Location - London or Winchester with hybrid working as per departmental requirements (currently a MINIMUM of 40% (2 days per week) with Tuesday as the team day. In 2020 LCP launched our Heath Analytics practice, providing analytical and research services for organisations across the life sciences and healthcare industries. Our team brings together health economists, statisticians, market access specialists, epidemiologists, clinicians, and health data scientists alongside our established actuarial, analytics and technology teams to deliver new solutions for the fundamental challenges in health. Our team's mission is to help move health systems from importers of illness to exporters of health and to support our clients to deliver value to patients. This is underpinned by our approach to support clients to improve the population's health and reduce inequalities. What's the role? LCP's Health Analytics team works across the healthcare and life sciences markets, combining health expertise with innovative approaches from our work in other sectors to tackle leading health issues. Examples of the types of projects that this role would cover, include, but are not limited to: Development of GVDs and other similar documents i.e. early value dossiers, AMCP and other formulary access tools (including payer value decks, US Pre-approval information exchange materials, and HEOR/ access toolkits), payer value propositions/ messages and objection handlers Supporting HTA dossier development JCA submission dossier development Literature review and statistical analysis reports Publications including posters, abstracts and manuscripts Development of data visualisation/ infographic type deliverables Conference, advisory board and other similar reports Providing strategic recommendations on global clinical trial design to enable HTA and reimbursement success Identifying optimal routes for access in different markets Landscape assessment, including but not limited to, competitor, pricing and reimbursement and HTA Patient journey mapping Secondary and primary research to validate market access strategies Payer evidence needs and gap analysis To support our continued growth, we are looking for an experienced Consultant with a proven track record in medical writing, particularly as applied to market access deliverables, to join our team and play a key role in growing our market access and value communication offerings. You'll have experience in writing and managing the development of a wide variety of market access/ value communication deliverables, including but not limited to, Global Value Dossiers (GVDs), American Managed Care Pharmacy (AMCP) dossiers, other payer formulary packs, payer value decks, HTA submissions, value driver identification and value story development, objection handlers, white papers, data visualisation tools, medical education, real world study reports, SLR reports, training materials, and market access/ HEOR/ RWE focused manuscripts. If you are looking to make a tangible impact, help develop a sub-service with an established service area (including team training and development of processes and editorial standards), take on leadership opportunities, and grow your expertise in a supportive and dynamic environment, then this is the role for you! Your key responsibilities will be to: Act as lead writer in the delivery of high-quality content which is fully referenced and reflective of the evidence base, and which is tailored to the target audience in terms of its content and style Lead market access focused projects including those that have a significant medical writing component. This will include coordination and project management of internal delivery teams alongside client-facing coordination of projects Develop Health Analytics team "house style" and similar editorial standards, processes and templates, while also being responsible for reviewing the work of other members of the team and contributing to team training and development of internal resources tools and processes People responsibilities including the line management and development of junior members of the team, depending on candidate's experience and interests Conduct targeted secondary research utilising a wide variety of sources to address specific research questions i.e., understand disease and competitor landscape, current treatment pathways, pricing and reimbursement processes, payer value drivers etc. Support the conduct of qualitative and quantitative payer research and analysis to identify opportunities and challenges for client products in various healthcare markets. This may include leading on the design of surveys, conducting 1:1 in-depth interviews, advisory boards, roundtable and other primary research methodologies Develop value messages, dossiers, and other related payer value communication materials e.g. payer value decks, toolkits, objection handlers and internal training materials Support the preparation of client-facing presentations and reports, effectively communicating complex concepts to diverse audiences. Manage projects (administrative and financial) including acting as the day-to-day client contact on projects, while also tracking and closely managing project budgets to ensure profitable and timely delivery Contribute to thought leadership, business development and marketing activities What skills, qualities and experience are we looking for? Essential Demonstrable experience as a market access medical writer in a consultancy environment, to include preparing market access and HEOR focused medical writing projects (including but not limited to; GVDs, HTA dossiers, early value dossiers, AMCP and other formulary access tools, manuscripts, conference presentations, payer value propositions/ messages and objection handlers)A 2:1 degree or better plus a science/ health-related postgraduate qualification (Masters or PhD) in a life-science focused subject or in an English language focused subject, with proven experience of application in the healthcare market access arenaDemonstrable experience of working in MS PowerPoint and prose-based, MS Word and similar formats is required.Confidence in leading the preparation of client-facing presentations and reports, effectively communicating complex concepts to diverse audiencesAbility to conduct and guide others in targeted secondary research utilising a wide variety of sources to address specific research questions. In addition, you should have a s
An exciting opportunity has arisen for a Materials Scientist to join a established chemical manufacturing company that is investing heavily in its future. This role offers excellent progression and development opportunities, a competitive salary of £35,000-£43,000, and a strong benefits package. As a full-time, permanent position based at their Accrington site, and is an ideal next step for a Mate click apply for full job details
Apr 29, 2026
Full time
An exciting opportunity has arisen for a Materials Scientist to join a established chemical manufacturing company that is investing heavily in its future. This role offers excellent progression and development opportunities, a competitive salary of £35,000-£43,000, and a strong benefits package. As a full-time, permanent position based at their Accrington site, and is an ideal next step for a Mate click apply for full job details
enior Development Scientist - Gas Metrology & Clean Energy Applications Location: Uttoxeter, Staffordshire Confidential - Specialist Gas Measurement Organisation An established global leader in gas metrology, calibration and analytical science is looking for a Senior Development Scientist to lead cutting edge research into gas quality and purity for the clean energy sector. This company provides expert measurement science, consultancy and calibration services to clients across energy, environmental, and industrial sectors - helping to set global standards in gas analysis and ensuring accuracy in hydrogen, CO , and LNG applications. The Opportunity You'll play a key role in advancing new analytical methods, instrumentation, and calibration standards. From hydrogen fuel cell impurity testing to CO purity measurement for carbon capture, this role will allow you to apply deep technical expertise across a range of innovative R&D programmes. Key Responsibilities Lead research and development projects in gas analysis, passivation, and purity measurement. Develop and validate new analytical instruments, methodologies and software tools. Oversee laboratory operations, ensuring UKAS accreditation and compliance with quality, safety and environmental standards. Provide technical leadership and consultancy, supporting clients in energy transition and emission reduction programmes. Prepare technical papers, grant applications and client presentations to promote the organisation's scientific capability. Contribute to the design and production of Primary Reference Gas mixtures and measurement standards. Background & Skills Degree (and ideally postgraduate qualification) in chemistry, physics, materials science or a similar discipline. Strong understanding of gas analysis, instrumentation, and calibration science. Experience developing or managing R&D projects within analytical or measurement environments. Excellent communication and reporting skills with the ability to engage clients and research partners. Proficiency in data analysis or basic programming would be advantageous. Why This Role? You'll join a respected, independent organisation that partners globally with energy majors, research institutions, and regulatory bodies to advance gas measurement accuracy and environmental integrity. Alongside competitive salary, performance bonus, and pension contributions, you'll benefit from flexible working, genuine career development, and the chance to contribute to next generation measurement standards in hydrogen and carbon capture. If you're passionate about applying scientific rigour to real world energy challenges, this is an outstanding opportunity to lead innovation in a world class technical environment. DCS Recruitment and all associated companies are committed to creating a working environment where diversity is celebrated and everyone is treated fairly, regardless of gender, gender identity, disability, ethnic origin, religion or belief, sexual orientation, marital or transgender status, age, or nationality
Apr 29, 2026
Full time
enior Development Scientist - Gas Metrology & Clean Energy Applications Location: Uttoxeter, Staffordshire Confidential - Specialist Gas Measurement Organisation An established global leader in gas metrology, calibration and analytical science is looking for a Senior Development Scientist to lead cutting edge research into gas quality and purity for the clean energy sector. This company provides expert measurement science, consultancy and calibration services to clients across energy, environmental, and industrial sectors - helping to set global standards in gas analysis and ensuring accuracy in hydrogen, CO , and LNG applications. The Opportunity You'll play a key role in advancing new analytical methods, instrumentation, and calibration standards. From hydrogen fuel cell impurity testing to CO purity measurement for carbon capture, this role will allow you to apply deep technical expertise across a range of innovative R&D programmes. Key Responsibilities Lead research and development projects in gas analysis, passivation, and purity measurement. Develop and validate new analytical instruments, methodologies and software tools. Oversee laboratory operations, ensuring UKAS accreditation and compliance with quality, safety and environmental standards. Provide technical leadership and consultancy, supporting clients in energy transition and emission reduction programmes. Prepare technical papers, grant applications and client presentations to promote the organisation's scientific capability. Contribute to the design and production of Primary Reference Gas mixtures and measurement standards. Background & Skills Degree (and ideally postgraduate qualification) in chemistry, physics, materials science or a similar discipline. Strong understanding of gas analysis, instrumentation, and calibration science. Experience developing or managing R&D projects within analytical or measurement environments. Excellent communication and reporting skills with the ability to engage clients and research partners. Proficiency in data analysis or basic programming would be advantageous. Why This Role? You'll join a respected, independent organisation that partners globally with energy majors, research institutions, and regulatory bodies to advance gas measurement accuracy and environmental integrity. Alongside competitive salary, performance bonus, and pension contributions, you'll benefit from flexible working, genuine career development, and the chance to contribute to next generation measurement standards in hydrogen and carbon capture. If you're passionate about applying scientific rigour to real world energy challenges, this is an outstanding opportunity to lead innovation in a world class technical environment. DCS Recruitment and all associated companies are committed to creating a working environment where diversity is celebrated and everyone is treated fairly, regardless of gender, gender identity, disability, ethnic origin, religion or belief, sexual orientation, marital or transgender status, age, or nationality
Arcinova, A Quotient Sciences Company Arcinova provides innovative contract research, development, and manufacturing services. We offer a comprehensive range of integrated specialist services for early stage drug development, underpinned by strong industry knowledge and scientific expertise. Our mission is to bring science, innovation, and collaboration together to overcome the barriers in drug development. We empower emerging biotechs and large pharma alike to bring life changing therapies to patients faster, through an efficient, effective approach focused on quality, science, and innovation. Our vision is to advance progress through science, delivering solutions that make a measurable difference. We look ahead with purpose, driven to shape a smarter, more resilient future for all. The Role We are looking for an Analytical Scientist to join our team in Alnwick on a permanent basis. In this role, you will develop, validate, and apply analytical methodologies within a regulated environment, ensuring full compliance with GLP/GMP guidelines. You will also provide expert advice and problem solving for specialized analytical techniques. Main tasks and responsibilities Analysis of drug substances, raw materials, intermediates and drug products using a variety of analytical techniques. Develop, validate and report analytical methodology and, where appropriate, provide resolution to technical problems. Apply analytical methodologies during the quality control and stability evaluation of a range of materials. Prepare work protocols for approval, critically assess data generated and review data from peers. Prepare and review reports, quality documents and training documentation. Acquire/record data in a manner that complies with GxP and internal policies/procedures. Perform assigned roles within Quality Control such as equipment responsible operator, training, equipment hardware and/or software validation and the ordering of consumable items. Work with due regard to health and safety of self and others. Work flexibly across the site to meet business needs - meaning adapting to changing priorities and tasks, not physical mobility or changes to working hours. We welcome different working needs and are happy to discuss any adjustments required. Qualifications and experience required BSc (Hons) or equivalent in a relevant scientific discipline. Experience in the application of analytical methodologies in a pharmaceutical environment is advantageous. Ability to communicate effectively in a way that supports collaboration. The ability to critically assess data and have a flexible approach to new work challenges. Competent in the use of Microsoft Office packages such as Word and Excel. Application Requirements When applying for a position with Quotient Sciences you must be aged 18 years or over and not have been debarred by the FDA. If you indicate you are under the age of 18 or have been debarred then your application will be automatically declined. Our Commitment to Diversity, Equity and Inclusion Quotient Sciences are advocates for positive change and conscious inclusion. We strive to create a diverse Quotient workforce and develop a workplace culture that provides a sense of acceptance for every person within our organization. As a global employer, we recognize the value in having an organization that is a true reflection and representation of our society today. Specifically we will not discriminate on the basis of race, color, creed, religion, gender, gender identity, pregnancy, marital status, partnership status, domestic violence victim status, sexual orientation, age, national origin, alienage or citizenship status, veteran or military status, disability, medical condition, genetic information, caregiver status, unemployment status or any other characteristic prohibited by federal, state and/or local laws. This applies to all aspects of employment, including hiring, promotion, demotion, compensation, training, working conditions, transfer, job assignments, benefits, layoff, and termination.
Apr 29, 2026
Full time
Arcinova, A Quotient Sciences Company Arcinova provides innovative contract research, development, and manufacturing services. We offer a comprehensive range of integrated specialist services for early stage drug development, underpinned by strong industry knowledge and scientific expertise. Our mission is to bring science, innovation, and collaboration together to overcome the barriers in drug development. We empower emerging biotechs and large pharma alike to bring life changing therapies to patients faster, through an efficient, effective approach focused on quality, science, and innovation. Our vision is to advance progress through science, delivering solutions that make a measurable difference. We look ahead with purpose, driven to shape a smarter, more resilient future for all. The Role We are looking for an Analytical Scientist to join our team in Alnwick on a permanent basis. In this role, you will develop, validate, and apply analytical methodologies within a regulated environment, ensuring full compliance with GLP/GMP guidelines. You will also provide expert advice and problem solving for specialized analytical techniques. Main tasks and responsibilities Analysis of drug substances, raw materials, intermediates and drug products using a variety of analytical techniques. Develop, validate and report analytical methodology and, where appropriate, provide resolution to technical problems. Apply analytical methodologies during the quality control and stability evaluation of a range of materials. Prepare work protocols for approval, critically assess data generated and review data from peers. Prepare and review reports, quality documents and training documentation. Acquire/record data in a manner that complies with GxP and internal policies/procedures. Perform assigned roles within Quality Control such as equipment responsible operator, training, equipment hardware and/or software validation and the ordering of consumable items. Work with due regard to health and safety of self and others. Work flexibly across the site to meet business needs - meaning adapting to changing priorities and tasks, not physical mobility or changes to working hours. We welcome different working needs and are happy to discuss any adjustments required. Qualifications and experience required BSc (Hons) or equivalent in a relevant scientific discipline. Experience in the application of analytical methodologies in a pharmaceutical environment is advantageous. Ability to communicate effectively in a way that supports collaboration. The ability to critically assess data and have a flexible approach to new work challenges. Competent in the use of Microsoft Office packages such as Word and Excel. Application Requirements When applying for a position with Quotient Sciences you must be aged 18 years or over and not have been debarred by the FDA. If you indicate you are under the age of 18 or have been debarred then your application will be automatically declined. Our Commitment to Diversity, Equity and Inclusion Quotient Sciences are advocates for positive change and conscious inclusion. We strive to create a diverse Quotient workforce and develop a workplace culture that provides a sense of acceptance for every person within our organization. As a global employer, we recognize the value in having an organization that is a true reflection and representation of our society today. Specifically we will not discriminate on the basis of race, color, creed, religion, gender, gender identity, pregnancy, marital status, partnership status, domestic violence victim status, sexual orientation, age, national origin, alienage or citizenship status, veteran or military status, disability, medical condition, genetic information, caregiver status, unemployment status or any other characteristic prohibited by federal, state and/or local laws. This applies to all aspects of employment, including hiring, promotion, demotion, compensation, training, working conditions, transfer, job assignments, benefits, layoff, and termination.
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. Tecnical Director's 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, the Technical Director 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 29, 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. Tecnical Director's 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, the Technical Director 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.
A pioneering quantum computing start-up is seeking an Applications Scientist in London to develop quantum algorithms with a focus on materials science and pharmaceuticals. The ideal candidate will have a PhD in a relevant field, experience in quantum chemistry or condensed matter physics, and a track record in quantum algorithms research. This role offers a competitive salary and share options within a dynamic and collaborative team culture, contributing to cutting-edge developments in quantum computing.
Apr 28, 2026
Full time
A pioneering quantum computing start-up is seeking an Applications Scientist in London to develop quantum algorithms with a focus on materials science and pharmaceuticals. The ideal candidate will have a PhD in a relevant field, experience in quantum chemistry or condensed matter physics, and a track record in quantum algorithms research. This role offers a competitive salary and share options within a dynamic and collaborative team culture, contributing to cutting-edge developments in quantum computing.
Join as a Founder in Residence in Climate We're on the lookout for entrepreneurial individuals with technical and commercial domain expertise with keen interest in founding, and building a global scale, impact driven, high growth company from ground up. We are seeking applications from experienced industry, startup and/or new science or engineering based technology development professionals from anywhere in the world to work with us on the next generation of plastics recycling. You'll work closely with the DSV team and the current Founder in Residence for this area to co found and spin out a new company. Once the new venture is incorporated with pre seed investment from DSV, you and your co founder(s) will own the majority stake in the business and continue receiving support from the DSV team post spinout. The role is full time, remote initially until venture incorporation and spin out (circa Q1 2026). The Opportunity We are building a venture to transform waste polyolefins into high value, recyclable degradable packaging materials. Our novel process produces polymers with properties comparable to polypropylene but with dramatically improved end of life characteristics, including solvolysis recyclability and environmental degradability. We are seeking a commercially focused co founder to partner with our technical founder and lead all commercial activities from company formation through Series A and beyond. This is a ground floor opportunity to shape a business addressing the urgent challenge of plastic circularity. Our Approach We are developing an electrified, contaminant tolerant process capable of transforming polyolefin waste into chemicals that will form the basis of a new materials platform. Initially, we will be focusing on developing new packaging materials to tackle the global plastic waste problem. Over time, we anticipate the technology will have applications in various other sectors. It is our hope that this technology will act as a global polyolefin sink - enabling global recovery and reuse of polyolefins. The developed materials will be simpler to recycle than current technologies, and will have environmental compatbility designed in from day one. In order for us to make our vision real we are seeking to recruit a commercially focused cofounder to support our near term commercial objectives. The Role As Commercial Co-Founder, you will own the commercial strategy and execution for the venture. Working alongside the technical founder, you will be responsible for validating market demand, building customer and supplier relationships, navigating regulatory pathways, and securing the commercial proof points required to raise successive funding rounds. This is a hands on role. In the early stages, you will personally conduct customer interviews, negotiate agreements, and build financial models. As the company grows, you will recruit and lead a commercial team. Who We're Looking For Must-Have Experience (one of the following core tracks): Previous experience in a startup or early stage company environment A track record in fundraising, grant writing, and grant management Exposure to regulatory processes for chemicals or materials, and a strong network across relevant industries such as plastics, packaging, or waste management Essential Capabilities: Lead customer discovery to identify and prioritise target markets, building relationships from initial outreach through to binding offtake agreements, and refining value proposition based on market feedback Identify and secure feedstock supply partnerships with waste management companies, and develop strategic partnerships with distributors, compounders, and brand owners Co develop and maintain techno economic models and pricing strategy with the founding team, and lead commercial negotiations and contract structuring Lead fundraising efforts with commercial due diligence materials, building investor relationships and communicating commercial progress Contribute to overall company strategy as a member of the founding team Demonstrated B2B sales and business development experience, ideally in materials, chemicals, or related industrial sectors, with a track record from cold outreach to signed agreements Strong negotiation skills, financial literacy including the ability to build and interrogate financial models, and experience fundraising from venture capital and grants Comfort making decisions with incomplete information and prioritising opportunities with scarce resources Understanding of chemicals, polymers, or materials industry dynamics Willingness to operate across strategic and administrative tasks, with resilience, strong self direction, and ability to thrive in uncertain environments Excellent communication skills with the ability to build credibility across diverse stakeholders, present to senior executives and investors, and work collaboratively with a technical co founder Ability to recruit and lead team members as the company grows, with a desire to build and scale an organisation aligned with company mission and values Valuable "Nice to Haves": Experience managing customer application testing programmes, developing go to market strategy, and assessing partnership structures including distribution, licensing, and joint development Experience building quality and customer service systems, and recruiting commercial team members Ability to scope and manage regulatory pathways, coordinate with consultants and certification bodies, and substantiate environmental claims Experience identifying and securing grant funding, and developing long term expansion strategy Familiarity with the waste market, circular economy trends in plastics, recycling value chains, and regulatory frameworks for chemicals and materials By joining DSV, you will be part of a team of operators who have founded companies and led the translation of science at some of the most respected universities, charities, funds, and government agencies. Here's what we offer: Access to optimised, purpose built, proprietary tools, resources, and processes to help create high impact ventures from scratch; Opportunity area specific know how from our network of Partners and Advisors; Up to £250k in investment to incorporate the new venture and develop early proof of concept data; Guaranteed income of £4,166 per month paid as a fixed consultancy fee until the company is launched and the pre seed investment is secured; Majority equity stake in the new company betweenyou and your co founder(s); Continuous post spinout support, including fundraising, commercial partnerships, recruitment, and team building; Collaborative support from dozens of Founders currently at DSV across sectors. About DSV Deep Science Ventures (DSV) is on a mission to create a future in which both humans and the planet can thrive. We use our unique venture creation process to create, spin out, and invest in science companies, combining available scientific knowledge and founder type scientists into high impact ventures. Operating in four sectors-Pharmaceuticals, Climate, Agriculture, and Computation-we tackle the challenges defining these areas by taking a first principles approach and partnering with leading institutions.
Apr 28, 2026
Full time
Join as a Founder in Residence in Climate We're on the lookout for entrepreneurial individuals with technical and commercial domain expertise with keen interest in founding, and building a global scale, impact driven, high growth company from ground up. We are seeking applications from experienced industry, startup and/or new science or engineering based technology development professionals from anywhere in the world to work with us on the next generation of plastics recycling. You'll work closely with the DSV team and the current Founder in Residence for this area to co found and spin out a new company. Once the new venture is incorporated with pre seed investment from DSV, you and your co founder(s) will own the majority stake in the business and continue receiving support from the DSV team post spinout. The role is full time, remote initially until venture incorporation and spin out (circa Q1 2026). The Opportunity We are building a venture to transform waste polyolefins into high value, recyclable degradable packaging materials. Our novel process produces polymers with properties comparable to polypropylene but with dramatically improved end of life characteristics, including solvolysis recyclability and environmental degradability. We are seeking a commercially focused co founder to partner with our technical founder and lead all commercial activities from company formation through Series A and beyond. This is a ground floor opportunity to shape a business addressing the urgent challenge of plastic circularity. Our Approach We are developing an electrified, contaminant tolerant process capable of transforming polyolefin waste into chemicals that will form the basis of a new materials platform. Initially, we will be focusing on developing new packaging materials to tackle the global plastic waste problem. Over time, we anticipate the technology will have applications in various other sectors. It is our hope that this technology will act as a global polyolefin sink - enabling global recovery and reuse of polyolefins. The developed materials will be simpler to recycle than current technologies, and will have environmental compatbility designed in from day one. In order for us to make our vision real we are seeking to recruit a commercially focused cofounder to support our near term commercial objectives. The Role As Commercial Co-Founder, you will own the commercial strategy and execution for the venture. Working alongside the technical founder, you will be responsible for validating market demand, building customer and supplier relationships, navigating regulatory pathways, and securing the commercial proof points required to raise successive funding rounds. This is a hands on role. In the early stages, you will personally conduct customer interviews, negotiate agreements, and build financial models. As the company grows, you will recruit and lead a commercial team. Who We're Looking For Must-Have Experience (one of the following core tracks): Previous experience in a startup or early stage company environment A track record in fundraising, grant writing, and grant management Exposure to regulatory processes for chemicals or materials, and a strong network across relevant industries such as plastics, packaging, or waste management Essential Capabilities: Lead customer discovery to identify and prioritise target markets, building relationships from initial outreach through to binding offtake agreements, and refining value proposition based on market feedback Identify and secure feedstock supply partnerships with waste management companies, and develop strategic partnerships with distributors, compounders, and brand owners Co develop and maintain techno economic models and pricing strategy with the founding team, and lead commercial negotiations and contract structuring Lead fundraising efforts with commercial due diligence materials, building investor relationships and communicating commercial progress Contribute to overall company strategy as a member of the founding team Demonstrated B2B sales and business development experience, ideally in materials, chemicals, or related industrial sectors, with a track record from cold outreach to signed agreements Strong negotiation skills, financial literacy including the ability to build and interrogate financial models, and experience fundraising from venture capital and grants Comfort making decisions with incomplete information and prioritising opportunities with scarce resources Understanding of chemicals, polymers, or materials industry dynamics Willingness to operate across strategic and administrative tasks, with resilience, strong self direction, and ability to thrive in uncertain environments Excellent communication skills with the ability to build credibility across diverse stakeholders, present to senior executives and investors, and work collaboratively with a technical co founder Ability to recruit and lead team members as the company grows, with a desire to build and scale an organisation aligned with company mission and values Valuable "Nice to Haves": Experience managing customer application testing programmes, developing go to market strategy, and assessing partnership structures including distribution, licensing, and joint development Experience building quality and customer service systems, and recruiting commercial team members Ability to scope and manage regulatory pathways, coordinate with consultants and certification bodies, and substantiate environmental claims Experience identifying and securing grant funding, and developing long term expansion strategy Familiarity with the waste market, circular economy trends in plastics, recycling value chains, and regulatory frameworks for chemicals and materials By joining DSV, you will be part of a team of operators who have founded companies and led the translation of science at some of the most respected universities, charities, funds, and government agencies. Here's what we offer: Access to optimised, purpose built, proprietary tools, resources, and processes to help create high impact ventures from scratch; Opportunity area specific know how from our network of Partners and Advisors; Up to £250k in investment to incorporate the new venture and develop early proof of concept data; Guaranteed income of £4,166 per month paid as a fixed consultancy fee until the company is launched and the pre seed investment is secured; Majority equity stake in the new company betweenyou and your co founder(s); Continuous post spinout support, including fundraising, commercial partnerships, recruitment, and team building; Collaborative support from dozens of Founders currently at DSV across sectors. About DSV Deep Science Ventures (DSV) is on a mission to create a future in which both humans and the planet can thrive. We use our unique venture creation process to create, spin out, and invest in science companies, combining available scientific knowledge and founder type scientists into high impact ventures. Operating in four sectors-Pharmaceuticals, Climate, Agriculture, and Computation-we tackle the challenges defining these areas by taking a first principles approach and partnering with leading institutions.
A leading AI research lab is seeking a qualified candidate for the Materials Discovery Laboratory. The role involves bridging theoretical and physical worlds by developing strategies for novel materials like superconductors. Responsibilities include executing synthesis workflows, leading structural characterizations, and collaborating with automation engineers to develop workflows. The position requires a PhD in a related field and experience in solid-state synthesis methodologies. The company promotes equal employment opportunities and diverse learning paths.
Apr 28, 2026
Full time
A leading AI research lab is seeking a qualified candidate for the Materials Discovery Laboratory. The role involves bridging theoretical and physical worlds by developing strategies for novel materials like superconductors. Responsibilities include executing synthesis workflows, leading structural characterizations, and collaborating with automation engineers to develop workflows. The position requires a PhD in a related field and experience in solid-state synthesis methodologies. The company promotes equal employment opportunities and diverse learning paths.
We are welcoming applications for policy internships to take place in 2026/27. Our policy internship scheme is open to all UK-based PhD students who have access to funding via their PhD programme to undertake an internship. MRC-funded applicants should apply via our specific AMS/MRC internship scheme. Our policy internship is designed to give students first hand experience of the medical science policy environment, to gain insights into how research can impact on policy, and to build valuable networks with the UK's most eminent medical scientists and key science and health stakeholders. You can read more about what our previous policy interns have worked on and gone on to do in our case study booklet. Applications are welcomed for 12-week internships taking place from July 2026 to June 2027. Applications will be considered as they come in. About the Academy of Medical Sciences The Academy of Medical Sciences is the independent, expert voice of biomedical and health research in the UK. Our elected Fellows are the UK's leading medical scientists from hospitals, academia, industry and the public service. Our vision is good health for all supported by the best research and evidence. Our mission is to help create an open and progressive research sector to improve the health of people everywhere. Our strategy for focuses on the following strategic priorities. Influence policy and practice to improve the lives of patients, the public and communities Support UK biomedical and health research to strengthen its global competitiveness and reputation Support the next generation of researchers to reach their full potential Work with our partners to increase the Academy's impact on global health Build our resources to ensure our long term independence and effectiveness Job description The Academy's policy work addresses issues of medical science, healthcare and biomedical careers. This work can take many forms: major reports, shorter position papers, seminars and workshops, correspondence, representation on Government and external panels, evidence to Parliamentary committees, private meetings and roundtables with key decision makers. During the 12-week internship, students will be involved in a variety of activities that will give them experience of many aspects of medical science policy and related activities. This will include one or more discrete projects led by the intern. The range of activities may include: Writing, editing, proofreading and referencing policy papers, e.g. responses to public consultations, papers and summaries for working groups, Council or Officers meetings. Desk based research and scoping, e.g. preparing project proposals or undertaking literature reviews. Evidence gathering and preparation, e.g. preparation of contacts lists, drafting calls for evidence, collating and summarising evidence. Events organisation, e.g. preparing conference materials, helping to co ordinate activities on the day. Attending (virtual) internal and external events, e.g. Parliamentary Select Committees, working group meetings, and lectures. Opportunities to observe policy professionals in other organisations. We believe that the policy internship at the Academy of Medical Sciences will: Provide future researchers and academic leaders with a deeper understanding of medical science policy. Develop a cadre of people able to work at the interface between medical science and policymaking. Allow students to build valuable contacts with senior scientists and policymakers, and expose them to the wide range of public, charitable and commercial organisations involved in UK medical science. Provide opportunities for PhD students to develop valuable transferable skills and to enhance their CVs. Eligibility The scheme is open to all UK-based PhD students (based in a university or institute), including clinicians undertaking a PhD as part of their Clinical Research Training. In order to be eligible, interns must have access to either: a three month extension to their PhD maintenance stipend, or funding for a three month placement integral to the programme . MRC-funded applicants should apply via our specific AMS/MRC internship scheme. The scheme can also be undertaken in the three month period immediately following the end of a student's PhD funding coming to an end. For example, if your funding ends in April, May or June 2026, you would be able to participate in the July 2026 to September 2026 placement. However, you would not be able to participate in any subsequent placements. Location of internship The Academy is based in central London and operates a hybrid working policy. Interns are encouraged to attend the office at least one day a week, and for occasional internal and external events. For interns based outside of London, we would anticipate that they would need access to funds to come to the Academy offices from time to time during their internships. We are open to discussing arrangements on a case by case basis. Timing of Internship The 2026/27 internship scheme will run four times: from July 2026 - September 2026, October 2026 - December 2026, January 2027 - March 2027 and April 2027 - June 2027. Application process To apply, candidates are asked to supply the following: An application form, including an endorsement and a supporting statement from their supervisor and an endorsement by the Programme sponsor (the PhD Programme Director). Download application form. A short covering letter briefly describing their reasons for application. A CV. A short article, of no more than 800 words in length, on a medical science policy topic. Applications should be submitted electronically and must be received by COP 11 May 2026. Interviews will be conducted on week commencing 25 May 2026. Please direct further questions to Jessamyn Briers: If you experience any technical difficulties with the form, please get in touch with Camelia Avramescu, People Assistant: . Placements on the scheme are allocated on a competitive basis so withdrawal from the scheme once a place is accepted is likely to result in another potential intern being denied the opportunity to participate.
Apr 28, 2026
Full time
We are welcoming applications for policy internships to take place in 2026/27. Our policy internship scheme is open to all UK-based PhD students who have access to funding via their PhD programme to undertake an internship. MRC-funded applicants should apply via our specific AMS/MRC internship scheme. Our policy internship is designed to give students first hand experience of the medical science policy environment, to gain insights into how research can impact on policy, and to build valuable networks with the UK's most eminent medical scientists and key science and health stakeholders. You can read more about what our previous policy interns have worked on and gone on to do in our case study booklet. Applications are welcomed for 12-week internships taking place from July 2026 to June 2027. Applications will be considered as they come in. About the Academy of Medical Sciences The Academy of Medical Sciences is the independent, expert voice of biomedical and health research in the UK. Our elected Fellows are the UK's leading medical scientists from hospitals, academia, industry and the public service. Our vision is good health for all supported by the best research and evidence. Our mission is to help create an open and progressive research sector to improve the health of people everywhere. Our strategy for focuses on the following strategic priorities. Influence policy and practice to improve the lives of patients, the public and communities Support UK biomedical and health research to strengthen its global competitiveness and reputation Support the next generation of researchers to reach their full potential Work with our partners to increase the Academy's impact on global health Build our resources to ensure our long term independence and effectiveness Job description The Academy's policy work addresses issues of medical science, healthcare and biomedical careers. This work can take many forms: major reports, shorter position papers, seminars and workshops, correspondence, representation on Government and external panels, evidence to Parliamentary committees, private meetings and roundtables with key decision makers. During the 12-week internship, students will be involved in a variety of activities that will give them experience of many aspects of medical science policy and related activities. This will include one or more discrete projects led by the intern. The range of activities may include: Writing, editing, proofreading and referencing policy papers, e.g. responses to public consultations, papers and summaries for working groups, Council or Officers meetings. Desk based research and scoping, e.g. preparing project proposals or undertaking literature reviews. Evidence gathering and preparation, e.g. preparation of contacts lists, drafting calls for evidence, collating and summarising evidence. Events organisation, e.g. preparing conference materials, helping to co ordinate activities on the day. Attending (virtual) internal and external events, e.g. Parliamentary Select Committees, working group meetings, and lectures. Opportunities to observe policy professionals in other organisations. We believe that the policy internship at the Academy of Medical Sciences will: Provide future researchers and academic leaders with a deeper understanding of medical science policy. Develop a cadre of people able to work at the interface between medical science and policymaking. Allow students to build valuable contacts with senior scientists and policymakers, and expose them to the wide range of public, charitable and commercial organisations involved in UK medical science. Provide opportunities for PhD students to develop valuable transferable skills and to enhance their CVs. Eligibility The scheme is open to all UK-based PhD students (based in a university or institute), including clinicians undertaking a PhD as part of their Clinical Research Training. In order to be eligible, interns must have access to either: a three month extension to their PhD maintenance stipend, or funding for a three month placement integral to the programme . MRC-funded applicants should apply via our specific AMS/MRC internship scheme. The scheme can also be undertaken in the three month period immediately following the end of a student's PhD funding coming to an end. For example, if your funding ends in April, May or June 2026, you would be able to participate in the July 2026 to September 2026 placement. However, you would not be able to participate in any subsequent placements. Location of internship The Academy is based in central London and operates a hybrid working policy. Interns are encouraged to attend the office at least one day a week, and for occasional internal and external events. For interns based outside of London, we would anticipate that they would need access to funds to come to the Academy offices from time to time during their internships. We are open to discussing arrangements on a case by case basis. Timing of Internship The 2026/27 internship scheme will run four times: from July 2026 - September 2026, October 2026 - December 2026, January 2027 - March 2027 and April 2027 - June 2027. Application process To apply, candidates are asked to supply the following: An application form, including an endorsement and a supporting statement from their supervisor and an endorsement by the Programme sponsor (the PhD Programme Director). Download application form. A short covering letter briefly describing their reasons for application. A CV. A short article, of no more than 800 words in length, on a medical science policy topic. Applications should be submitted electronically and must be received by COP 11 May 2026. Interviews will be conducted on week commencing 25 May 2026. Please direct further questions to Jessamyn Briers: If you experience any technical difficulties with the form, please get in touch with Camelia Avramescu, People Assistant: . Placements on the scheme are allocated on a competitive basis so withdrawal from the scheme once a place is accepted is likely to result in another potential intern being denied the opportunity to participate.
Principal Mechanical Engineer page is loaded Principal Mechanical Engineerremote type: Hybridlocations: Cambridgetime type: Full timeposted on: Posted 2 Days Agojob requisition id: R45925Xylem is a Fortune 500 global water solutions company dedicated to advancing sustainable impact and empowering the people who make water work every day. As a leading water technology company with 23,000 employees operating in over 150 countries, Xylem is at the forefront of addressing the world's most critical water challenges. We invite passionate individuals to join our team, dedicated to exceeding customer expectations through innovative and sustainable solutions.Sentec, a Xylem brand, seeks to hire an Principal Mechanical Engineer to lead our talented mechanical engineering skill group.As Principal, you will lead a mechanical engineering team on high-value, technically challenging projects, internal to Xylem and external clients. You will own mechanical architecture and key technical decisions and act as subject-matter expert in mechanical design, materials, and manufacturing. You will deliver innovative mechanical solutions from early concept through detailed design and industrialisation and validation testing. You will work directly with Xylem partners and external clients to understand requirements and translate them into robust engineering solutions, contribute to project planning, technical reporting and support proposal writing, technical scoping, and effort estimation.As a senior colleague, you will mentor and develop junior and mid-level engineers and scientists, foster a collaborative, high-performance engineering culture and set engineering best practice. You will also be responsible for supporting project management as well as business development activities under the guidance of the respective teams. The position is largely based in our Cambridge office however you will have the opportunity for some travel, this could be UK-wide, within Europe, the United States or the Far East. At Sentec you will be working in a rapidly evolving industry at an exciting time for technologists developing solutions in multiple sectors with a strong emphasis on sustainability. In order to be successful you will need to demonstrate leadership in pursuit of technical solutions and novel ideas, have a hands-on approach to problem solving and ultimately managing projects against time, budget and client expectations. This role combines hands-on engineering, technical decision-making, project and team leadership within a fast-paced consultancy environment spanning multiple sectors, working towards deadlines and delivering excellent technical solutions. You will be required to communicate effectively in a wide range of environments, both with colleagues and clients and will have the opportunity to develop your negotiation skills and expand your technical knowledge. Minimum Qualifications: Education, Experience, Skills, Abilities, License/Certification: Extensive experience (10+ years) in mechanical engineering / product development Experience in people leadership, preferably in mechanical engineering Strong 3D CAD capability (principally Creo but SolidWorks also advantageous) Proven experience taking products from concept to manufacture Hands-on experience making parts and building prototypes Experience dealing with 3rd party suppliers such as engineering workshops, plastic fabricators, hardware suppliers Excellent understanding of materials, tolerancing, and manufacturing processes Experience working in multidisciplinary teams (physics, electronics, software) Minimum 2/1 Degree (or equivalent) in Mechanical Engineering or related discipline Desirable Skills/Knowledge: Background in consultancy or contract R&D environments Experience with machinery such as lathes and milling machines Experience with 3D printing, both internal and bureau Experience in one or more sectors such as: Sensing technology such as optical, magnetic, ultrasonic Consumer and industrial products Scientific instrumentation Water infrastructure Sustainable energy Knowledge of regulatory or quality systems (e.g. ISO 13485, ISO 9001) Experience with FEA, thermal analysis, or other simulation Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Regularly required to sit or stand, reach, bend and move about the facility Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Office: Standard office equipment; work usually performed in an office or site laboratory setting Estimated 10 % or less travel requirement Standard weekly job hours: 37.5 hours Benefits Include: Competitive salaries Holiday of 25 days per year, increases with length of service Group life cover at 4 times basic salary Private health care Salary sacrifice pension scheme Relocation expenses as appropriate Annual performance and merit process Discretionary 10% All staff bonus scheme Employee referral bonus scheme Access to flexible benefits including cycle to work, critical illness cover and green car leasing Flexible and remote workingJoin the global Xylem team to be a part of innovative technology solutions transforming water usage, conservation, and re-use. Our products impact public utilities, industrial sectors, residential areas, and commercial buildings, with a commitment to providing smart metering, network technologies, and advanced analytics for water, electric, and gas utilities. Partner with us in creating a world where water challenges are met with ingenuity and dedication; where we recognize the power of inclusion and belonging in driving innovation and allowing us to compete more effectively around the world.background, skills and interests.
Apr 28, 2026
Full time
Principal Mechanical Engineer page is loaded Principal Mechanical Engineerremote type: Hybridlocations: Cambridgetime type: Full timeposted on: Posted 2 Days Agojob requisition id: R45925Xylem is a Fortune 500 global water solutions company dedicated to advancing sustainable impact and empowering the people who make water work every day. As a leading water technology company with 23,000 employees operating in over 150 countries, Xylem is at the forefront of addressing the world's most critical water challenges. We invite passionate individuals to join our team, dedicated to exceeding customer expectations through innovative and sustainable solutions.Sentec, a Xylem brand, seeks to hire an Principal Mechanical Engineer to lead our talented mechanical engineering skill group.As Principal, you will lead a mechanical engineering team on high-value, technically challenging projects, internal to Xylem and external clients. You will own mechanical architecture and key technical decisions and act as subject-matter expert in mechanical design, materials, and manufacturing. You will deliver innovative mechanical solutions from early concept through detailed design and industrialisation and validation testing. You will work directly with Xylem partners and external clients to understand requirements and translate them into robust engineering solutions, contribute to project planning, technical reporting and support proposal writing, technical scoping, and effort estimation.As a senior colleague, you will mentor and develop junior and mid-level engineers and scientists, foster a collaborative, high-performance engineering culture and set engineering best practice. You will also be responsible for supporting project management as well as business development activities under the guidance of the respective teams. The position is largely based in our Cambridge office however you will have the opportunity for some travel, this could be UK-wide, within Europe, the United States or the Far East. At Sentec you will be working in a rapidly evolving industry at an exciting time for technologists developing solutions in multiple sectors with a strong emphasis on sustainability. In order to be successful you will need to demonstrate leadership in pursuit of technical solutions and novel ideas, have a hands-on approach to problem solving and ultimately managing projects against time, budget and client expectations. This role combines hands-on engineering, technical decision-making, project and team leadership within a fast-paced consultancy environment spanning multiple sectors, working towards deadlines and delivering excellent technical solutions. You will be required to communicate effectively in a wide range of environments, both with colleagues and clients and will have the opportunity to develop your negotiation skills and expand your technical knowledge. Minimum Qualifications: Education, Experience, Skills, Abilities, License/Certification: Extensive experience (10+ years) in mechanical engineering / product development Experience in people leadership, preferably in mechanical engineering Strong 3D CAD capability (principally Creo but SolidWorks also advantageous) Proven experience taking products from concept to manufacture Hands-on experience making parts and building prototypes Experience dealing with 3rd party suppliers such as engineering workshops, plastic fabricators, hardware suppliers Excellent understanding of materials, tolerancing, and manufacturing processes Experience working in multidisciplinary teams (physics, electronics, software) Minimum 2/1 Degree (or equivalent) in Mechanical Engineering or related discipline Desirable Skills/Knowledge: Background in consultancy or contract R&D environments Experience with machinery such as lathes and milling machines Experience with 3D printing, both internal and bureau Experience in one or more sectors such as: Sensing technology such as optical, magnetic, ultrasonic Consumer and industrial products Scientific instrumentation Water infrastructure Sustainable energy Knowledge of regulatory or quality systems (e.g. ISO 13485, ISO 9001) Experience with FEA, thermal analysis, or other simulation Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Regularly required to sit or stand, reach, bend and move about the facility Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Office: Standard office equipment; work usually performed in an office or site laboratory setting Estimated 10 % or less travel requirement Standard weekly job hours: 37.5 hours Benefits Include: Competitive salaries Holiday of 25 days per year, increases with length of service Group life cover at 4 times basic salary Private health care Salary sacrifice pension scheme Relocation expenses as appropriate Annual performance and merit process Discretionary 10% All staff bonus scheme Employee referral bonus scheme Access to flexible benefits including cycle to work, critical illness cover and green car leasing Flexible and remote workingJoin the global Xylem team to be a part of innovative technology solutions transforming water usage, conservation, and re-use. Our products impact public utilities, industrial sectors, residential areas, and commercial buildings, with a commitment to providing smart metering, network technologies, and advanced analytics for water, electric, and gas utilities. Partner with us in creating a world where water challenges are met with ingenuity and dedication; where we recognize the power of inclusion and belonging in driving innovation and allowing us to compete more effectively around the world.background, skills and interests.
