Beschreibung
Task:- Remediation of existing Production Risk Management documentation.
Requirements (Must have):
- Three or more years manufacturing and/or quality experience with prior experience in the manufacture of medical devices or pharmaceuticals preferred.
- 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.
- Fluent (spoken and written) in English and German.
Beginn: 18.04.2016
Dauer: 31.12.2016
Branche: Dienstleistung