A number of exciting roles have just become available in the Regulatory Affairs field.

We are currently recruiting for a number of Senior positions within our Medical Device and Diagnostic client companies in Clare, Offaly and Galway.


Key Responsibilities:

  • Support the manufacturing of electrical/mechanical medical devices and related components and accessories.
  • Review and approve all related change orders and performs the necessary regulatory assessments, working with a larger regulatory team to determine pre-approval requirements.
  • Development and maintenance of EU product files including Class III design dossiers and Class IIb, IIa and Is technical files which facilitate timely regulatory approvals.



  • Honours Degree in a related discipline
  • Over 3 years experience in supporting manufacturing of medical devices.
  • Proven skills in the developing CE registrations.

Why Apply?

  • Leadership standalone roles allowing the successful candidate full autonomy.
  • Suitable for candidates with a Senior QA background
  • All Permanent positions available
  • Full benefits including an attractive remuneration package
  • Salary EUR45K+


Apply Now
Please Contact

Aoife Judge,
Senior Consultant

Specialisation: Manufacturing / Contingent

Office: Shannon   |   View Aoife’s Jobs

Aoife is MSc qualified in Work and Organisational Behaviour and possesses a BSc in Human Resource Management, with a career background in Human Resources and Healthcare and Technical Recruitment. She joined CREGG in 2015 specialising in the areas of Science, Quality and Engineering in the Mid-West Region – before moving into Contingent Recruitment.


Aoife account manages a number of highly regulated clients in the Mid-West Region and has successfully built and maintained strong professional relationships so as to allow her to work in partnership with them, to meet their specific needs.