Beschreibung
Task:Focus: Technical Files Remediation Risk
- 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).
- BS in Engineering (or science) required.
- Proficient in Microsoft Office (Excel, Word, etc.).
- Fluent (spoken and written) in English and German.
- GMP
- ISO regulations
Beginn: asap
Dauer: 23.12.2016
Branche: Medizin/Healthcare