The role involves ensuring operational quality on the factory floor to guarantee compliance with Good Manufacturing Practices during production shifts
Job Summary
The role involves ensuring operational quality on the factory floor to guarantee compliance with Good Manufacturing Practices during production shifts.
Candidates will be responsible for reviewing lot dossiers, leading investigations into deviations and out-of-specification results, and verifying corrective actions.
GSK Evreux is a major pharmaceutical manufacturing site producing respiratory medications and employs approximately 1,000 people.
Matching Summary
The role involves ensuring operational quality on the factory floor to guarantee compliance with Good Manufacturing Practices during production shifts.
Skills & Requirements
Must-have
Minimum 1 year GMP manufacturing experience
Lot release and dossier review skills
Investigation of deviations and OOS/OOT incidents
CAPA tracking and verification expertise
Strong oral and written French communication
Nice-to-have
Internal audit and external inspection preparation
Experience with Veeva or SAP systems
Continuous improvement project leadership
Data analysis for quality initiatives
Previous operational QA on large production sites
Key Requirements
Diploma in Pharmacy, Engineering (Chemistry/Biology), or equivalent
Minimum 1 year experience in GMP manufacturing environment