Regulatory Reviewer. Medical Devices. CONTRACT. Switzerland

Vertragsart:
Vor Ort
Start:
keine Angabe
Dauer:
11 months
Von:
MBA - Muenchen
Ort:
Solothurn
Eingestellt:
04.09.2013
Land:
flag_no Schweiz
Projekt-ID:
593512

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ASAP - June 2014

Top 20 Medical Device Company

Solothurn, Switzerland

German Speaking Essential

60-100 CHF per Hour

Excellent opportunity for a medical device professional with 6 months - 5 years of experience to join the team of a global medical device company (class III implantable devices for orthopaedics) and to be an important part of their ongoing compliance project. Your role will be focused on reviewing Technical Files (SOPs) and Change Requests, with broader responsibilities made available in quality engineering, regulatory labelling and scientific writing. Prior experience in working to European or Global medical device regulations (classes I, II or III) is essential.

I look forward to hearing form you, this role offers a competitive hourly rate, a job description is available on request.

Kind regards,

Michael

Job Code: 96351

Michael Bailey International is acting as an Employment Business in relation to this vacancy.