Beschreibung
Aufgaben:- Remediation of existing Production Risk Management documentation
- Functional Experience Requirements
- Manufacturing and/or quality experience with prior experience in the manufacture of medical devices or pharmaceuticals preferred
Qualifikationen:
- Strong background in Production Risk
Management with experience in creation, review, and approval of risk
management documentation (PFMEAs or DFMEAs) - Strong analytical skills
- BS in Engineering (or science) required
- Ability to effectively manage multiple priorities and tasks
- Fluent (spoken and written) in English and German