Regulatory Affairs Specialist

Job Overview

My client, a leading medical device manufacturing company are seeking a
Regulatory Affairs Specialist to join their team on a Permanent contract. There is an excellent salary package plus benefits on offer for the right candidate.

Your new position:
As Reg Affairs Specialist you will be responsible for the development, and maintenance of regulatory submissions, documentation, annual reporting etc as required.

Responsibilities:
- Assisting the team with a number of key projects
- Dossier preparation to support generics portfolio.
- Licensing support for new drug developments some are authorised (one with an NDA in
- Assisting with veterinary portfolio regulatory strategy
- Liasing with regulatory agencies (FDA and EMA) on filing strategy and dossier content

What You'll Need To Succeed:
- A passion for Regulatory Affairs
- A degree in Chemistry or Pharmacy (or a related discipline)
- 2+ years Regulatory experience (CMC focused Pharma experience considered)

What you'll get in return:
You will be remunerated with an attractive salary along with bonus and generous holiday allowance 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. Imagine working in a cutting edge world-class manufacturing environment where the demands are great but where there is ample opportunity to progress your career and advance your technical expertise with an employer that put a premium on talent development and employee engagement.

Your Next Step:
To apply for this position, please submit your CV through this website now in the strictest of confidence.

Have some questions? Call me for more information: Leo Cordingley 086 0495443

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