Product Risk Management Medical Devices

For our client a Medical Device and Diagnostics company based in Zuchwil we are currently looking for a PRODUCT DEVELOPEMENT/QUALITY ENGINEER

Start: 11 February 2014

End: 30.09.14

Location: Zuchwil, Oberdoft, Waldenburg

OVERALL RESPONSIBILITIES:

. Remediation of existing Risk Management documentation (Design & Clinical Risk Management, Risk Management Report, and Risk Management Plan) to the Product Risk Management Process.

Functional Experience Requirements

. Three or more years 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).

. Strong analytical skills.

Required Degree/Certificates:

. BS in Engineering (or science) required.

Competencies:

. Proficient in Microsoft Office (Excel, Word, etc.).

. Ability to effectively manage multiple priorities and tasks.

. Excellent communication skills.

Specific Languages:

. Fluent (spoken and written) in English and German.

PLEASE NOTE THAT THESE ROLES ARE BASED IN:

Oberdorf, Waldenburg, ZuchwilMichael Bailey International is acting as an Employment Business in relation to this vacancy.