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About the Client An important company within the biopharmaceutical / biotech sector, with a cutting-edge facility in Valais. This international company is known worldwide 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. You'll liaise 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 Ph.D. in biology, biochemistry, or pharmaceuticals
Experience in GMP environments and quality control
Proficiency in German and English
Knowledge/experience with pharmaceutical/laboratory software (e.g., Documentum, LIMS, Trackwise) is a plus
Additional Details Location: Valais, Switzerland
Work Experience: QA Manual Test, General Project Management, IT Consultant
Languages: English
Seniority Level: Entry level
Employment Type: Full-time
Job Function: Quality Assurance
Industries: Technology, Information and Internet
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