Scientist - Bioanalytical LC in Manchester

This role is ideal for an experienced bioanalytical LC-MS/MS scientist who enjoys working independently, applying technical expertise to complex quantitative analysis, and collaborating closely with colleagues and clients. You will bring strong technical capability, confidence in method development and validation, and the ability to communicate clearly on both scientific and commercial matters.

Required skills and experience:

• BSc, MSc or PhD in Chemistry, Biology, or a related scientific discipline
• In-depth knowledge of LC-MS/MS, with 5+ years' experience supporting pre-clinical and clinical bioanalysis
• Proven experience in quantitative LC-MS/MS method development and validation
• Practical understanding of the requirements of Pharmacokinetic (PK) analysis and ICH M10 Bioanalytical Method validation guidance
• Experience working in a GxP-regulated laboratory with a strong understanding of GMP, GLP and GCP
• Practical experience extracting small and/or large molecules from biological matrices (e.g. plasma, serum, urine)
• Strong problem-solving skills, with the ability to work autonomously and apply scientific literature where required
• Good IT, numeracy and data interpretation skills
• Clear written and verbal communication skills, with confidence engaging directly with clients
• Strong organisational skills, with the ability to manage multiple projects and meet delivery timelines

About the opportunity:

You will work as an independent member of the Bioanalytical LC-MS/MS team, delivering high-quality quantitative bioanalytical services to pharmaceutical and bioanalytical clients. The role involves working across projects of varying scale, scope and complexity, with opportunities to apply specialist knowledge, develop new techniques, and contribute to both technical delivery and commercial success.

Key activities:

• Perform independent quantitative LC-MS/MS method development and validation with minimal supervision
• Plan, execute and interpret bioanalytical work, generating high-quality data and reports
• Deliver analytical services in accordance with GMP, GLP and GCP standards
• Ensure studies meet quality, regulatory and client expectations across clinical phases
• Troubleshoot complex bioanalytical challenges and develop fit-for-purpose solutions
• Communicate confidently with clients on technical requirements, results and analytical strategies
• Support Business Development through technical input into quotations and project planning
• Demonstrate commercial awareness when planning and delivering analytical work
• Support the training and mentoring of junior colleagues
• Collaborate proactively with colleagues across teams to ensure efficient project delivery

All work will be carried out in accordance with Intertek procedures, regulatory standards, and safety requirements.

What we offer:

• Join Intertek and become part of our global network of inspiring and entrepreneurial colleagues.
• We are a global family that values diversity and we thrive working together with precision, pace, and passion.
• We are working to make the world Ever Better, ensuring the quality, safety and sustainability of products and services used by millions of people around the world.
• Competitive salary/benefits
• Development and career opportunities around the Globe
• Working in a highly motivated team and dynamic working environment

We are an Equal Opportunity Employer who do not discriminate against applicants. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex or national origin.