Quality Manager – Sterile Manufacturing

Looking for more visibility responsibility and impact in Quality

Join a specialized sterile pharmaceutical manufacturing site where you will work closely with Production QA QC and the Qualified Person driving GMP compliance and operational quality activities in a highly regulated environment.

Your Responsibilities

• Support batch review and release activities
• Review GMP documentation and manufacturing records
• Manage deviations CAPAs and Change Controls
• Provide quality support to production laboratories and warehouse operations
• Maintain strong shopfloor presence and drive continuous improvement
• Act as compliance contact for customers and external partners
• Support inspections and client audits

Your Profile

• Degree in Pharmacy Chemistry Life Sciences or Engineering
• Experience in GMP-regulated pharmaceutical manufacturing
• Strong exposure to sterile / aseptic production
• Experience with deviations investigations and Change Controls
• Operational mindset and willingness to work close to production
• Fluent French and good English

Whats on Offer

• High visibility role within a specialized pharmaceutical manufacturing site
• Broad quality responsibilities with direct impact on operations
• Close collaboration with Production QA QC and Release teams
• International environment with short decision paths
• Excellent opportunity to further develop towards broader Quality and QP responsibilities