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Medical Device CEMA

Medical Device CEMA

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Medical Device CEMA

Well respected client requires a dynamic consultant to join the team The regulations in certain countries and regions require the registrations of new products, perform renewals for the life cycle management and to do change submissions according to the national regulations.

Duties

  • New product registrations
  • Life cycle management
  • Change submissions
  • Change impact assessments
  • RA releases in SAP
  • Work with product and license databases
  • Input for regulatory requests related to medical devices in the respective CEMA-region
  • Coordination of regulatory activities with other departments

Experience

  • 2-4 Years Reg affairs Medical Devices

Please contact Phil Turner or email your resume for an immediate response