CK Group are recruiting for a Quality Auditor, to join a biopharmaceutical company, on a contract basis for 6 months.

PLEASE NOTE:

This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
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• Be responsible for the final review of clinical batch records.
• Compilation and approval of data packs and presentation to the QP for final release.
• Conducts routine audits of data, information, procedures, equipment and systems.
• Review and approve production and analytical documentation accompanying the release of API, Safety Assessment or clinical supply lots.
• Perform audits or inspections of assigned areas or systems to assess compliance with regulatory and Company standards.