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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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