We are partnering with a global medical device business who are based in Yorkshire. They have an impressive turnover and currently are looking for a regulatory affairs specialist who’s got strong experience with Technical file remediation and MDR transition.
As the Regulatory Affairs Specialist you will be responsible for:
Maintaining all technical files and regulatory documents
Providing accurate medical device regulatory and quality guidance to the rest of the business
Ensuring products comply with ISO 13485
Preparing documents for regulatory submissions
Three years’ experience within the medical device industry in regulatory affairs
An understanding of both MDR and MDD regulations.
Strong knowledge guideline ISO13485
You can contact me confidentially on 02030196024 or firstname.lastname@example.org