Quality Manager – Sterile Manufacturing

Quality Manager – Sterile Manufacturing
French\-Speaking Switzerland \| GMP \| Quality \& Compliance
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
What’s 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 jpid4b59698jm jpit0730jm jpiy26jm