Stem Recruitment have a couple of opportunities for experienced RA's based near Edinburgh for a medical device company.
The roles are responsible for:
1. Building regulatory strategy.
2. Determining applicable regulatory requirements.
3. Proposing solutions to comply with regulatory requirements.
4. Managing product license registration with the appropriate regulatory authorities worldwide.
5. Building, implementing, and maintaining regulatory compliance processes, including regulatory evaluation of changes and non-conformances, post-market surveillance, vigilance, and associated reporting, regulatory and standard watch.
Requirements include:
* A relevant degree and/or relevant work experience in a regulatory affairs environment.
* Experience in the medical device / IVD / biotech industry.
* Experience in post-market surveillance.
If this is of interest, please get in touch for a confidential conversation.
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