Job title: Regulatory Affairs Specialist Location: Parkmore, Galway.
1-2 days a week on site Benefits: Top salary, Bonus, pension, healthcare, hybrid working Overview: My client are a fast-paced, rapidly growing medical device company offering a highly differentiated solution in vascular interventions.
With a culture of innovation helping each individual develop both professionally and personally, and our culture of respect means that they all work in a collaborative, empowering, and exciting environment.
Responsibilities: - Approval of Vigilance/MDR reporting as defined in each territory.
- Support and lead Regulatory Post Market System improvements.
- Participate in the implementation of Field Safety Corrective Action plan and associated activities if required.
- Manage RA activities for Design Changes and Supplier-related changes including reporting assessment and generation of regulatory submissions.
- Provide RA Support to relevant Design Teams for Key Projects identified by Veryan.
- Provide support to other RA Specialists in achieving success for the team.
- Manage and support trend data for regulatory reporting - Support Gap Assessment process and associated process improvements.
- Management of PMA Annual Periodic Reporting system and approval of annual documentation for submission to FDA.
Requirements: A degree level qualification in Engineering, Science, QA, or related field is essential.
A minimum of 2 years experience at a regulatory level in the medical device industry is essential.
Experience of FDA guidance for sterile implantable products in premarket approvals is desirable.
Technical competency of ISO, ISO 14971, MDR 2017/745, and the FDA QSRs is a prerequisite.
Does this sound like your next career move? To apply and For more info forward your application to the link provided or contact me on OR