This vacancy has been reviewed by the Intranet desk. We guarantee verified employer standing, salary transparency, and zero applicant fees.
Corporate RegistrationUK Companies House active incorporation
Prevailing Wage ComplianceUK National Living Wage & Equality Act aligned
Right-to-Work FitUK Work Eligibility
Zero Processing Charges100% Free direct candidate application
SPONSORED CAREER ADVISORYAD
Position Overview & Specifications
Ensuring compliance with GMP and other regulatory requirements; be the Quality point of contact for CMC external parties; manage the review and timely closure of manufacturing and/or release and stability testing deviations or change controls.
Responsible for management of the CMC part of the annual External/Supplier audit programme
To provide guidance for higher level decisions required for change management and deviation investigations, as required.
The preferred candidate for the role will have extensive experience in GB and EU GMP regulated environments and would have acted as quality manager in a pharmaceutical or Biotechnology organisation with Biologics manufacturing experience. The ideal candidate will also have good understating of IMP manufacturing and extensive expertise of EU, MHRA and FDA requirements
If you are interested in this opportunity, please send your up-to-date CV to Oliver@BlackfieldAssociates.com or call Oliver on 02392 314 792.
STR Limited is acting as an Employment Agency in relation to this vacancy.
INTERNATIONAL TALENT PLACEMENT NETWORKSPONSORED
Ready to Apply for this Role?
Submit your credentials directly through our verified pipeline with 100% zero placement or recruiter fees.
🛂United Kingdom Skilled Worker & Right to Work Guide
UK positions require valid Right to Work. For sponsored visas under the points-based immigration system, the employer must hold an active A-rated Home Office sponsor license and issue a Certificate of Sponsorship (CoS) meeting minimum income thresholds (£38,700 or going rate).