Description
For my client, a global medical devices company I am currently seeking a Risk Management Specialist for an 8 months project in Switzerland.Start: ASAP
Duration: asap - 30.09.2014
Location: Switzerland
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.
Requirements:
- BS in Engineering (or science) required.
- Proven experience within risk management
- 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.
I am a specialized recruiter and I am currently taking care of more than 20 freelance projects within the Medical Devices area in Switzerland. For more information about this role or jobs within related specialist areas please send me your CV with your hourly rate expectation for immediate consideration.
Keywords: risk management, dfmeas, pfmeas, freelance/temporary, German, English, Switzerland
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