About this job

Fantastic opportunity has arisen to join a world-leading pharmaceutical testing CRO.

We are looking for an enthusiastic Equipment Compliance Specialist with a broad knowledge of analytical chemistry equipment.

In this role, you will be responsible for:

• Checking instrument calibration & service data for multiple GMP analytical equipment (HPLC, dissolution, Karl Fischer, etc.)
• Updating & writing SOPs
• Supporting internal audits
• Liaising closely with analysts & team leaders to ensure GMP standards are adhered to
• Authorising quality documents (Installation Qualification (IQ), Performance Qualification (PQ), Operational Qualification (OQ))

Qualifications/Skills/Experience:

• Degree in Chemistry or related subject
• Pharmaceutical analysis experience in a GMP environment
• Strong knowledge of various analytical chemistry techniques and instrumentation
• Qualification and validation of analytical equipment is a plus!
• Strong communication and organisation skills

If this role sounds like the right opportunity for you, apply today to be considered!

Keywords: Pharmaceutical, Biopharmaceutical, API, Drug Product, Intermediate, GMP, cGMP, Good Manufacturing Practise, HPLC, UPLC, high performance liquid chromatography, LC, LCMS, LC-MS, GC, gas chromatography, Analytical Chemistry, analyst, SOP, documentation, validation, qualification, IQ, PQ, OQ, Wirral, Liverpool, Moreton, Cheshire, Manchester, North West, Ellesmere Port, Runcorn, Chester, Crewe, VRS8911MF

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