- Location
- Switzerland
- Workplace
- Onsite
- Type
- full-time
- Department
- Management and Consulting
- Seniority
- Manager
- Education
- Bachelor
- Industry
- Pharmaceuticals
- Category
- Quality Assurance
- Role type
- Individual Contributor
- Environment
- Industrial
- Source
- JOIN
Description
## 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
Skills
GMPCAPAChange ControlDeviation ManagementBatch ReleaseSterile ManufacturingAseptic ProcessingQuality Management Systems
Languages
FrenchEnglish
