Regulatory Affairs Manager Cosmetics/Medical Devices

My client is an innovating, dynamic and growing international pharmaceutical and healthcare company currently expanding their Global Regulatory Affairs team in Switzerland, Vaud Canton. Due to this growth my client is looking for a Global Regulatory Affairs Manager with experience working on Cosmetics/Medical Devices Products at global level.

Your Responsibilities

  • Setting up the regulatory strategy for projects under development
  • Coordinates the preparation and participates to meetings with Health Authorities/Notified Bodies if necessary
  • Communication of project relevant RA information to Project Team and Department Heads
  • Represents RA for medical devices or cosmetics in global & cross functional meetings
  • Provides regulatory support to ensure the content of dossier/technical files is compliant with relevant regulations and is sufficient for submission
  • Updates Product Information periodically or upon specific request
  • Ensures regulatory support for new product launch
  • Maintains and tracks RA activities databases
  • Supports the development of labelling and artworks

Your Profile

  • Minimum 5 years of prior experience in global Regulatory Affairs in the Consumer Care environment Cosmetics and Medical Devices.
  • PhD (in Sciences, Medicine or Pharmacy), Master or any equivalent advanced scientific degree in a related technical field
  • Strong knowledge of the cosmetic and medical devices industry, including solid knowledge of all associated global RA regulations

For more information, please contact : Noémie Oliva: noliva@axepta.com

Noemie OLIVA

Noemie OLIVA

Team leader & Recruitment Manager Life Sciences

Morgane CAYUELA

Morgane CAYUELA

Life Sciences Recruitment Specialist

Marine DOLLAT

Marine DOLLAT

Life Sciences Recruitment Specialist

Regulatory Affairs Manager Cosmetics/Medical Devices

Oct 7, 2021Regulatory Affairs Manager Cosmetics/Medical DevicesCanton of Vaud 18 months contract noliva@axepta.com Life Sciences

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