Responsibilities:
1. Provide engineering support for manufacturing unit operations and troubleshoot production issues to identify root causes.
2. Analyze equipment and process performance data to drive reliability, efficiency, and continuous improvement initiatives.
3. Execute engineering projects and support process changes to reduce factory losses and operational inefficiencies.
4. Participate in risk assessments using tools such as FMECA and PFMEA.
5. Collaborate closely with manufacturing, quality, validation, and maintenance teams to ensure seamless operations.
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. A minimum of 2 years of experience in a regulated industry (, pharmaceutical, biotechnology, medical device, or similar)
8. Fluency in English and German
What will give you a competitive edge (preferred qualifications):
9. Experience within pharmaceuticals or biotechnology or bio-pharma manufacturing operations
10. Strong knowledge of GMP (Good Manufacturing Practice) standards
11. Familiarity with data analysis tools for process optimization
12. Proven experience leading or supporting technical risk assessments
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