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
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