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We are supporting a growing and forward-thinking API manufacturer within the medical and nutraceutical sector in their search for a GMP Quality Control Analyst. This is an excellent opportunity for someone with industrial or commercial laboratory experience using HPLC who is looking to contribute to a quality-driven, regulated manufacturing environment. In this role, you will play a key part in ensuring products are tested, compliant, and manufactured to the highest regulatory standards. You’ll work closely with Production and Quality Assurance teams to maintain GMP compliance and deliver accurate, reliable analytical results.
Job Responsibility:
Perform analytical and physical testing of Active Pharmaceutical Ingredients (API)
Conduct HPLC analysis (assay and impurities) within an industrial/commercial laboratory environment
Support production schedules through timely and accurate testing
Work collaboratively with Production and Quality Assurance teams to ensure GMP compliance
Accurately record, analyse, and report results in line with regulatory requirements
Contribute to maintaining controlled manufacturing processes aligned with international regulatory standards
Requirements:
Bachelor’s degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Forensic Science, or related discipline (or equivalent experience)
Proven industrial or commercial laboratory experience using HPLC (assay and impurity analysis)
Experience in QC testing of APIs
Strong understanding of GMP environments
Good working knowledge of Microsoft Office (Word, Excel)
Excellent attention to detail and data accuracy
Ability to prioritise workload and adapt to changing priorities
Effective written and verbal communication skills
Right to work in the UK
Nice to have:
Experience using GC
Experience with additional wet chemistry techniques