Responsibilities:
1. Provide technical engineering support and act as a Subject Matter Expert (SME) for fermentation, lyophilization, aseptic filling, utilities, and packaging.
2. Lead process improvement initiatives, technology transfers, and scale-up projects to enhance reliability, efficiency, and product quality.
3. Manage deviations, CAPAs, change controls, and equipment qualification activities (IQ/OQ/PQ) within a GMP environment.
4. Resolve complex process or equipment issues by leading root cause investigations and cross-functional taskforces.
5. Drive operational excellence while providing technical leadership and mentorship to operational teams.
What You Need to Succeed (minimum qualifications):
6. Bachelor’s or Master’s degree in Process Engineering, Chemical Engineering, Bioprocess Engineering, Mechanical Engineering, or related discipline
7. Experience in pharmaceutical or biopharmaceutical manufacturing within a GMP regulated environment
8. Excellent communication skills with the ability to collaborate across functions and leadership levels
What will give you a competitive edge (preferred qualifications):
9. Fluency in English and German
10. Experience with GMP manufacturing unit operations
11. Proven experience with equipment qualification (IQ/OQ/PQ) and process validation
12. Experience leading engineering projects or continuous improvement initiatives
WHAT WE OFFER YOU
13. Interesting and varied working environment in a modern and growing global company in the pharmaceutical industry
14. Room for initiative and flexibility
15. Exciting development opportunities
16. Company fitness program
17. Meal allowance
18. Corporation benefits
19. Team events
20. Up to 30 days holiday
21. Special leave days (wedding, work anniversaries etc.)
22. Attractive remuneration according to the company collective agreement incl. Christmas and holiday bonus
23. 38 hours/week