Beschreibung
PRODUCT DEVELOPEMENT/QUALITY ENGINEER
Remediation of existing Risk Management documentation (Design & Clinical Risk Management, Risk Management Report, and Risk Management Plan) to the Product Risk Management Process.
Requirements:
. 3 or more years experience in the design and development of medical devices or pharmaceuticals
. Strong background in Product Risk Management with experience in creation, review, and approval of risk management documentation (DFMEAs and PFMEAs).
. BS in Engineering (or science) required.
. Ability to effectively manage multiple priorities and tasks.
. Excellent communication skills.
. Fluent (spoken and written) in English and German.
Others:
Start: 05/05/14 or ASAP
End: 31/12/14
Hourly rate: Negotiable
Travel: up to 5% in Switzerland
Location: Kanton Solothurn or Basel-Country
CONTACT:
Frank Arnold
PHARMACEUTICAL RECRUITMENT CONSULTANT
Michael Bailey International is acting as an Employment Agency in relation to this vacancy
Michael Bailey International is acting as an Employment Business in relation to this vacancy.