Remote - Regulatory Affairs Associate (Medical Devices)

  • Life Science People
  • Not Specified, Not Specified
  • Sep 11, 2020
Permanent

Job Description

Responsibilities:

* Assist in the preparation and submission of regulatory applications and registrations .
* Evaluate regulatory risks of corporate policies.
* Provide input for product development and planning throughout the product life cycle.
* Assist in correspondence with review agencies, notified bodies, and trade associations on matters relating to product registrations and PMS..
* Utilise technical regulatory skills to advise on MDR implementation.
* Work across Regulatory and Quality functions ensuring timely advice and insight...... click apply for full job details