Beschreibung
Product Development / Quality Engineers (m/w)- Remediation of existing Risk Management documentation to the Product Risk Management Process.
- BS in Engineering (or science)
- experience with prior experience in the design and development of medical devices or pharmaceuticals preferred
- Strong background in Product Risk Management with experience in creation, review, and approval of risk management documentation (DFMEAs and PFMEAs)
- Proficient in Microsoft Office
- Fluent (spoken and written) in English and German
Anforderung:
s.o
Projektstart: asap
Projektende: 30.9.2014 + Option
Auslastung: 5 Tage / Woche
Leistungsort: Solothurn (CH)
Direktbewerbung: hier