Senior Regulatory Affairs Specialist

Job Overview

We have an excellent opportunity for a Senior Regulatory Affairs Specialist to join a fast-growing medical technology company based in Cork

What's in it for you? This is a superb opportunity to work in for an innovative and friendly medical technology company that serve patients with life-improving treatments. Working here will be a fantastic addition to your CV. Your work will truly make a difference to people's lives and you will work alongside cutting-edge technology and a supportive and friendly team. Working here you will really make a difference.

Your new position: As Senior Regulatory Affairs Specialist you will be responsible for activities which lead to, and maintain regulatory approval to market devices. You will also be responsible for the assessment of device changes for regulatory implications and ensuring continued compliance with regulatory agency approvals.

What You'll Need To Succeed
- Degree-Level Qualification & 2+ years' reg affairs experience in the medical device or pharmaceutical industries
- U.S. and/or International medical device submissions experience
- Basic understanding of medical device regulations along with a general understanding of product development process and design control
- Ability to communicate complex ideas clearly and simply both orally and in writing

What you'll get:
You will be remunerated with an attractive salary along with pension, healthcare, life assurance. You will be part of a focused team who work together and support one another with their workloads. The atmosphere is friendly and all employees are supported by peers and managers.

NEXT STEPS: If you are looking for a new and challenging role with an exceptional company, please submit your application today or call Leo on 086 049 5443 for a confidential discussion on this fantastic Cork-based role.

Key Contact

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