MSAT Process Expert
(m/f/d)
Freelance/temporary employment for a project Visp Start date: asap Reference number: 858035/1
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Responsibilities
1. Establish and maintain strong customer relationships
2. Plan, prepare and oversee production campaigns from a QC perspective
3. Manage GMP-relevant change requests and deviations
4. Support and host customer audits and regulatory inspections
5. Calculate, track and report QC cost elements within assigned projects
6. Coordinate, prioritize and schedule QC activities independently
7. Ensure close alignment with QA, OPS, MSAT, engineering and other stakeholders
8. Lead cross-functional QC project activities without direct reports
9. Drive continuous improvement within QC operations and project workflows
10. Represent QC in tech transfers and ensure analytical readiness
Profile
11. Master’s or PhD in a natural science discipline (biology, biochemistry, pharmaceuticals or related field)
12. Solid industry experience
13. Proven experience in microbial GMP environments
14. Strong background in biomanufacturing, production operations, MSAT and tech-transfer
15. Experience in GMP quality control and analytical project coordination is an advantage
16. Proficient in MS Office; knowledge of Documentum, LIMS, Trackwise or similar software is an advantage
17. Strong organizational abilities, fast comprehension and high attention to detail
18. Ability to remain calm, structured and solution-oriented in dynamic or stressful situations
19. Conversational German and fluent English
Benefits
20. Opportunity to work at a leading biomanufacturing site with cutting-edge technologies
21. Cross-functional exposure across QC, QA, MSAT, engineering, production and program management
22. Independent role with high visibility and impact on customer projects
23. Dynamic, international environment with strong focus on teamwork and scientific excellence