Sanofi UK is seeking a Quality Assurance Specialist for a 6-month on-site position in Ocoyoacac, Mexico. The role involves ensuring compliance with quality systems and Good Manufacturing Practices (GMP) in the production of monovalent influenza antigens
Job Summary
Ensure compliance with Quality Systems, verifying adherence to Good Manufacturing Practices (GMP), Global Quality Directives, and corporate requirements for Antigene Monovalent production.
Manage the investigation process for deviations detected in various Quality Systems, GMP tasks, and operations, ensuring root cause identification and corrective/preventive actions.
Verify compliance with monitoring plans for services and facilities related to manufacturing, including HVAC, Water, Compressed Air, Nitrogen, and environmental monitoring.
Matching Summary
Match Score: 85
Sanofi UK is seeking a Quality Assurance Specialist for a 6-month on-site position in Ocoyoacac, Mexico. The role involves ensuring compliance with quality systems and Good Manufacturing Practices (GMP) in the production of monovalent influenza antigens.
Skills & Requirements
Must-have
Good Manufacturing Practices (GMP)
Quality Systems Compliance
Deviation Management Process
Data Integrity Assurance
Contamination Control Strategy
Nice-to-have
Attention to detail
Preventive focus
Autonomous work
Negotiation skills
Decision making
Key Requirements
Experience in Quality Assurance within the pharmaceutical industry
Intermediate language skills
Bachelor's degree in Biotechnology, Pharmaceutical Engineering, Chemical Pharmaceutical, Chemical Pharmaceutical Biologist, Pharmaceutical Biologist, etc.