Small 100 – 1000
Regulatory Affairs / /
Freelance Regulatory Affairs Consultant (Cosmetic Medical Devices) Roles – Full time, Immediate start We are seeking a Freelance Regulatory Affairs consultant to support a Cosmetics/Medical Device client based in the Auvergne-Rhône-Alpes region across responsibilities in: – Risk management – MDR Transition – CE Mark – Global registrations – Technical files – General compliance activities – Clinical investigation/study support This is a 6 month contract, full time, starting ASAP. There is some on site presence required which is negotiable. If you are interested in the role and available to start in the next month please reach out to schedule a call to discuss the role further. This role is moving fast, with multiple vacancies, and the client is looking to interview people on early next week, so please reply at your earliest convenience.
FTE / nb of days per week
Auvergne Rhone Alpes Area, France, France
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