Are you someone who thrives at the intersection of science, strategy, and collaboration?
About the Client
An important company within the biopharmaceutical / biotech sector, with a cutting edge facility in Valais. This international company is known across the world as a leader in the life sciences. They develop and manufacture medicines that protect millions of people from illness and disease. The company fosters a values-driven culture focused on collaboration, integrity, and innovation.
About the role
In this role, you'll be the go-to person for all things Quality Control within cross-functional project teams. Acting as the single point of contact, you'll work closely with production, QA, engineering, and external partners to ensure alignment and smooth execution across the board.
You'll be in close contact with analytical labs, program managers, and process development teams. Your ability to plan, prioritize, and adapt will be key to delivering projects on time and within budget-even when customer needs shift.
Responsibilities
- Maintain the quality of production.
- Build and maintain strong relationships with customers.
- Lead the planning and oversight of production campaigns.
- Manage GMP-related changes and deviations.
- Support audits and regulatory inspections.
- Track and manage QC-related project costs.
- Coordinate and schedule QC activities independently.
Requirements
- Master's or PhD in biology, biochemistry or pharmaceuticals.
- Experience in GMP environments and quality control.
- Good German and Englishs kills are a must.
- Knowledge/experience with pharmaceutical/laboratory software (e.g. Documentum, LIMS, Trackwise) is a pre.
