14 Analytical Chemistry jobs in the United Kingdom

• Lead the development, validation, and implementation of advanced analytical methods for complex chemical samples.
• Design and execute experiments using a wide range of analytical techniques (e.g., HPLC, GC-MS, LC-MS, NMR, ICP-MS, spectroscopy).
• Provide expert interpretation of analytical data, troubleshooting complex issues, and proposing innovative solutions.
• Mentor and guide junior scientists and technicians, fostering a culture of scientific excellence and collaboration.
• Oversee the maintenance and calibration of sophisticated analytical instrumentation.
• Contribute to the strategic planning of analytical services and research projects.
• Author and review scientific reports, protocols, and publications.
• Ensure compliance with all relevant regulatory guidelines (e.g., GMP, GLP) and internal quality standards.
• Collaborate effectively with cross-functional teams, including research scientists, process chemists, and quality assurance personnel.
• Stay abreast of the latest advancements in analytical chemistry and relevant scientific fields.

• PhD in Analytical Chemistry, Organic Chemistry, or a closely related field.
• A minimum of 8-10 years of progressive experience in analytical chemistry, with a strong focus on method development and validation.
• Extensive hands-on experience with a broad spectrum of modern analytical instrumentation and techniques.
• Proven expertise in data analysis, interpretation, and reporting.
• Demonstrated leadership and mentoring capabilities.
• Strong problem-solving skills and the ability to think critically and creatively.
• Excellent written and verbal communication skills, with the ability to present complex scientific information clearly.
• Familiarity with regulatory environments such as GMP and GLP.
• Ability to work effectively both independently and as part of a multidisciplinary team.
• A commitment to scientific integrity and a passion for innovation.

Quality Control - Stability & Analytical Chemistry | Harwell, Oxfordshire | 12-Month Contract | Full-Time Onsite | Up to 22.00 per hour, depending on experience .

Join a leading pharmaceutical team establishing a new facility in Harwell focused on mRNA therapeutics. You'll support vaccine production for respiratory diseases, work with advanced analytical tools and digital platforms, and collaborate with experts across academia, the NHS, and government.

Key Responsibilities:

• Perform analytical chemistry and stability testing using HPLC, UPLC, GC, UV, Karl Fischer, DLS, and other techniques.
• Support testing of raw materials, components, in-process samples, and drug substances.
• Complete cGMP documentation for all analytical work in compliance with regulatory standards.
• Enter data into LIMS (LabVantage) and complete electronic assay forms for traceability.
• Conduct HPLC (AEX) and NaOH plate-reader assays for manufacturing stat testing.
• Prepare reagents, manage inventory, maintain equipment, and ensure lab housekeeping.
• Ensure safe laboratory operations and contribute to EHS compliance.
• Manage procurement and stock of lab consumables and supplies.

Stability Program Duties:

• Execute stability operations including set down, pull, labelling, verification, inventory updates, and disposal.
• Author, review, and revise stability protocols, SOPs, and technical reports.
• Maintain and trend stability data, perform statistical analyses, and ensure real-time study visibility.
• Coordinate sample shipment and testing data with external labs.
• Update internal databases and binders with stability information.
• Support regulatory submissions and ensure alignment with FDA, EU, and ICH guidelines.

Additional Responsibilities:

• Troubleshoot analytical methods and instrumentation as needed.
• Train and mentor junior staff.
• Contribute to investigations, deviations, CAPAs, and change controls.
• Promote a positive, inclusive, and collaborative team culture.
• Ensure adherence to GDP, data integrity, and internal SOPs.
• Complete all required training and qualifications per assigned learning plans.

Candidate Requirements:

• BA/BSc in Chemistry, Biology, or a related scientific discipline.
• 5-7 years of experience in a pharmaceutical Quality Control laboratory.
• Strong understanding of GxP regulations (GMP, GLP, GCP, etc.).
• Comfortable working with digital platforms, LIMS systems, and data-driven workflows.
• Must be available to work full-time onsite at the Harwell facility.
• May be subject to enhanced pre-employment background checks.

Ideal Mindset:

• Eager to learn and adapt quickly in a highly technical and regulated environment.
• Digitally fluent and enthusiastic about using code and automation to improve outcomes.
• Collaborative and committed to fostering a positive team culture.

Should you require any support or assistance, please contact your local Gi Group office.

Gi Group Holdings Recruitment Limited are proud founding members of Menopause in business, pledge members for Neurodiversity in business, Disability committed members, Gold status pledge members for the Armed Forces Covenant, and Bronze trail blazers for Racial Equality matters.

Gi Group of companies includes Gi Group Holdings Recruitment Ltd, Gi Recruitment Ltd, Draefern Ltd, Excel Resourcing (Recruitment Consultants) Ltd, Gi Recruitment Ltd, INTOO (UK) Ltd, Marks Sattin (UK) Ltd, TACK TMI UK Ltd, TACK International Ltd, Grafton Professional Staffing Ltd, Encore Personnel Services Ltd, Gi Group Staffing Solutions Ltd and Gi Group Ireland Ltd. Gi Group Staffing Solutions Ltd are acting as an Employment Business in relation to this role.

We are committed to protecting the privacy of all our candidates and clients. If you choose to apply, your information will be processed in accordance with the Gi Group Privacy Statement. To view a copy and to help you understand how we collect, use and process your personal data please visit the Privacy page on our Gi Group website.

Quality Control - Stability & Analytical Chemistry | Harwell, Oxfordshire | 12-Month Contract | Full-Time Onsite | Up to 22.00 per hour, depending on experience .

Join a leading pharmaceutical team establishing a new facility in Harwell focused on mRNA therapeutics. You'll support vaccine production for respiratory diseases, work with advanced analytical tools and digital platforms, and collaborate with experts across academia, the NHS, and government.

Key Responsibilities:

• Perform analytical chemistry and stability testing using HPLC, UPLC, GC, UV, Karl Fischer, DLS, and other techniques.
• Support testing of raw materials, components, in-process samples, and drug substances.
• Complete cGMP documentation for all analytical work in compliance with regulatory standards.
• Enter data into LIMS (LabVantage) and complete electronic assay forms for traceability.
• Conduct HPLC (AEX) and NaOH plate-reader assays for manufacturing stat testing.
• Prepare reagents, manage inventory, maintain equipment, and ensure lab housekeeping.
• Ensure safe laboratory operations and contribute to EHS compliance.
• Manage procurement and stock of lab consumables and supplies.

Stability Program Duties:

• Execute stability operations including set down, pull, labelling, verification, inventory updates, and disposal.
• Author, review, and revise stability protocols, SOPs, and technical reports.
• Maintain and trend stability data, perform statistical analyses, and ensure real-time study visibility.
• Coordinate sample shipment and testing data with external labs.
• Update internal databases and binders with stability information.
• Support regulatory submissions and ensure alignment with FDA, EU, and ICH guidelines.

Additional Responsibilities:

• Troubleshoot analytical methods and instrumentation as needed.
• Train and mentor junior staff.
• Contribute to investigations, deviations, CAPAs, and change controls.
• Promote a positive, inclusive, and collaborative team culture.
• Ensure adherence to GDP, data integrity, and internal SOPs.
• Complete all required training and qualifications per assigned learning plans.

Candidate Requirements:

• BA/BSc in Chemistry, Biology, or a related scientific discipline.
• 5-7 years of experience in a pharmaceutical Quality Control laboratory.
• Strong understanding of GxP regulations (GMP, GLP, GCP, etc.).
• Comfortable working with digital platforms, LIMS systems, and data-driven workflows.
• Must be available to work full-time onsite at the Harwell facility.
• May be subject to enhanced pre-employment background checks.

Ideal Mindset:

• Eager to learn and adapt quickly in a highly technical and regulated environment.
• Digitally fluent and enthusiastic about using code and automation to improve outcomes.
• Collaborative and committed to fostering a positive team culture.

Should you require any support or assistance, please contact your local Gi Group office.

Gi Group Holdings Recruitment Limited are proud founding members of Menopause in business, pledge members for Neurodiversity in business, Disability committed members, Gold status pledge members for the Armed Forces Covenant, and Bronze trail blazers for Racial Equality matters.

Gi Group of companies includes Gi Group Holdings Recruitment Ltd, Gi Recruitment Ltd, Draefern Ltd, Excel Resourcing (Recruitment Consultants) Ltd, Gi Recruitment Ltd, INTOO (UK) Ltd, Marks Sattin (UK) Ltd, TACK TMI UK Ltd, TACK International Ltd, Grafton Professional Staffing Ltd, Encore Personnel Services Ltd, Gi Group Staffing Solutions Ltd and Gi Group Ireland Ltd. Gi Group Staffing Solutions Ltd are acting as an Employment Business in relation to this role.

We are committed to protecting the privacy of all our candidates and clients. If you choose to apply, your information will be processed in accordance with the Gi Group Privacy Statement. To view a copy and to help you understand how we collect, use and process your personal data please visit the Privacy page on our Gi Group website.

• Designing, executing, and optimizing complex analytical experiments using state-of-the-art instrumentation.
• Developing and validating novel analytical methods for the characterization of diverse chemical entities.
• Performing advanced data analysis and interpretation, drawing meaningful conclusions to guide research efforts.
• Troubleshooting analytical instrumentation and experimental procedures to ensure data integrity and reliability.
• Collaborating closely with interdisciplinary research teams to achieve project objectives.
• Preparing detailed technical reports, research summaries, and presentations for internal stakeholders and external conferences.
• Contributing to the intellectual property portfolio through invention disclosures and patent applications.
• Mentoring and supervising junior research scientists and laboratory technicians.
• Ensuring strict adherence to laboratory safety protocols and quality management systems.
• Staying abreast of the latest advancements in analytical chemistry and relevant scientific fields.
• Managing project timelines, resources, and budgets for assigned research initiatives.
• Contributing to the strategic direction of the research department and identifying new areas of scientific exploration.

• Lead the development, optimization, and validation of novel analytical methods for characterization of complex chemical entities and materials.
• Operate and maintain advanced analytical instrumentation, including but not limited to HPLC, GC-MS, LC-MS, NMR, ICP-MS, and spectroscopy techniques.
• Troubleshoot and resolve complex analytical issues, ensuring data integrity and reliability.
• Design and execute experimental plans to support research and development objectives.
• Interpret and present complex analytical data clearly and concisely to internal teams and external collaborators.
• Stay abreast of the latest advancements in analytical chemistry techniques and instrumentation.
• Mentor junior scientists and provide technical guidance on analytical challenges.
• Contribute to the preparation of technical reports, scientific publications, and regulatory documentation.
• Collaborate effectively with cross-functional teams, including synthetic chemists, material scientists, and process engineers.
• Ensure compliance with all relevant safety and quality standards in a remote laboratory setting.

• Ph.D. or Master's degree in Analytical Chemistry, Chemistry, or a related scientific discipline.
• Minimum of 7 years of progressive experience in analytical chemistry research and development.
• Extensive hands-on experience with a wide array of analytical instrumentation and methodologies.
• Proven expertise in method development and validation according to industry standards.
• Strong understanding of chemical principles and their application in analytical techniques.
• Excellent problem-solving, critical thinking, and data interpretation skills.
• Exceptional written and verbal communication skills, with the ability to present complex scientific information effectively.
• Demonstrated ability to work independently and manage multiple complex projects simultaneously in a remote environment.
• Familiarity with Good Laboratory Practices (GLP) or Good Manufacturing Practices (GMP) is desirable.
• Must be legally authorized to work in the UK.

• Lead the development and validation of advanced analytical methods for diverse sample types using techniques such as LC-MS/MS, GC-MS, ICP-MS, NMR, and hyphenated techniques.
• Design and execute complex analytical experiments to support discovery and development programs.
• Provide expert interpretation of analytical data and guide research teams in understanding chemical compositions and structures.
• Troubleshoot and resolve challenging analytical problems, ensuring data accuracy and reliability.
• Mentor and guide junior scientists, fostering scientific excellence and professional development within the analytical team.
• Collaborate with cross-functional teams, including synthetic chemists, biologists, and engineers, to define analytical requirements and solve research challenges.
• Stay at the forefront of analytical science, evaluating and implementing new technologies and instrumentation.
• Contribute to scientific publications, patents, and presentations.
• Ensure compliance with all relevant laboratory safety standards, quality management systems, and regulatory guidelines.
• Manage analytical project timelines and resources effectively.

• PhD in Analytical Chemistry, Physical Chemistry, or a closely related field.
• A minimum of 10 years of post-doctoral research experience in an industrial or academic R&D setting, with a significant portion focused on analytical challenges.
• Demonstrated expertise in a broad range of advanced analytical instrumentation and methodologies.
• Proven track record of leading complex analytical projects and delivering innovative solutions.
• Strong understanding of statistical analysis and data interpretation techniques.
• Excellent scientific leadership, mentoring, and communication skills.
• Ability to work effectively in a multidisciplinary team environment.
• Experience with LIMS and data management systems is desirable.
• Published extensively in peer-reviewed journals.
• A commitment to scientific rigor and innovation.

• Develop, validate, and optimize analytical methods.
• Operate and maintain advanced analytical instrumentation (HPLC, GC-MS, LC-MS, NMR, etc.).
• Analyze and interpret complex chemical data.
• Troubleshoot analytical issues and implement solutions.
• Collaborate with multidisciplinary research teams.
• Contribute to scientific publications and presentations.
• Ensure compliance with quality and regulatory standards.
• Mentor and guide junior research scientists.
• Contribute to the strategic direction of analytical research.

• Ph.D. in Analytical Chemistry or a closely related field.
• Extensive experience with a broad range of analytical techniques and instrumentation.
• Proven expertise in method development and validation.
• Strong data interpretation and problem-solving skills.
• Experience with scientific writing and presentations.
• Excellent collaborative and communication abilities.
• Familiarity with Good Laboratory Practice (GLP) or similar quality systems.
• Ability to work effectively in a hybrid work model.