Beschreibung
Aufgabe:- Remediation of existing Production Risk Management documentation.
Anforderung:
- 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).
- Ability to effectively manage multiple priorities and tasks.
- Excellent communication skills.
- Fluent (spoken and written) in English and German.
Umgebung/Sonstiges:
Fulltime
Beginn: 26.08.2013
Dauer: 31.12.2013
Branche: Dienstleistung