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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