Specialist Abweichungsmanagement Manufacturing (m/w/d) - Penzberg
Roche(1 month ago)
About this role
As part of the Quality Event Management team at Roche Pharma Manufacturing in Penzberg, you support the production of active pharmaceutical ingredients and commercial products used in Phase III clinical trials. The role centers on deviation management in a GMP-regulated manufacturing environment, helping ensure product quality and regulatory compliance. The position is offered as a two-year fixed-term contract.
Required Skills
- Deviation Management
- Root Cause
- Risk Assessment
- Continuous Improvement
- Problem Solving
- Project Management
- Time Management
- GMP Documentation
- Team Facilitation
- Technical Writing
+3 more
Qualifications
- Technician Certificate (Chemistry/Biotechnology)
- Degree in Technical or Natural Sciences
- Several Years GMP Production Experience
About Roche
roche.comAs a pioneer in healthcare, we have been committed to improving lives since the company was founded in 1896 in Basel, Switzerland. Today, Roche creates innovative medicines and diagnostic tests that help millions of patients globally.
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