My client is a world leader in food, environment and pharmaceutical product testing. They are also one of the market leaders in testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing.

The primary purpose of this role will be to develop and optimise analytical methods along with method validation and transfer according to regulatory guidelines. The role will involve participating in a team to ensure the highest quality and productivity standards are met along with the agreed client requirements and timelines.

• Perform analytical testing, data interpretation, and compound characterization with strict adherence to documentation and GMP standards.

• Develop, validate, and optimize analytical methods; support method transfer for new product introductions.

• Troubleshoot analytical and technical issues during development and validation phases.

• Communicate effectively with clients to provide updates, resolve queries, and deliver projects on time.

• Ensure timely delivery of projects while meeting site quality, safety, and technical KPIs.

• Review and approve SOPs, lab documentation, investigations, and risk assessments.

• Lead and support laboratory investigations, applying scientific rationale and root-cause analysis.

• Drive continuous improvement projects and identify efficiency gains in lab operations.

• Provide training and mentorship to analysts; ensure equipment and supply readiness.

• Promote best practices in compliance, ethical standards, and client service excellence.

• An honours degree in Chemistry or a related discipline is required.

• At least 5 years’ experience in an analytical laboratory.

• Extensive knowledge of Method development and Method validation

• Has experience of the analysis of APIs, raw materials and excipients and the associated analytical techniques that may include chromatographic (HPLC, GC, IC), spectroscopic (IR, LC-MS, ICP-OES, Atomic Absorption), physical properties (particle size analysis) and/or pharmacopoeial testing.

• Is highly proficient in the use of common laboratory instruments and software packages for the above analytical techniques.

• Experienced in problem solving and has expertise in troubleshooting both analytical equipment and methodology. 

• Possesses a thorough understanding of laboratory procedures

• Deep understanding of data integrity and the importance of adopting this guidance when reporting results / everyday work.

• Is competent in application of statistical and mathematical tools and formulae

• Is aware of relevant national / international pharmaceutical regulatory requirements.

• Thorough understanding of requirements for working in a GMP environment.

• Ability to quickly learn new processes.

• Ability to communicate clearly and to form strong working relationships with colleagues.

• Ability to work on own initiative and be capable of developing solutions to problems as part of a team.

• Willing to operate in a flexible manner and be able to switch priorities at short notice.

• Good team player, organised, accurate, have strong documentation skills.

• Passionate about quality and customer service.