Senior Regulatory Affairs Specialist

In this role you will report to the Regulatory Affairs Manager and you will provide input into regulatory strategies, performing activities associated with obtaining and maintaining regulatory approval to commercialise medical devices in selected target markets and providing regulatory affairs input for the functional areas. Candidates with Pharmaceutical or other similar regulated industry experience will be considered but must have staff management or supervisory experience.

Candidates with the following background and experience are invited to apply:

•    Third level Qualification preferably in Science/Quality, 5 years’ experience in a regulated industry in a similar role is desirable.
•    Knowledge of medical device quality standards/practises or similar regulated industry.
•    Good communication and inter-personal skills.
•    Proven problem-solving skills.
•    Good computer skills including knowledge of Microsoft® Office.
•    Proven organisational skills.
•    High self-motivation.
•    Willingness and availability to travel on company business.

For a full Job Spec and to apply for this role please call Deirdre on +353 1 2784671 or e-mail dbolger@thornshaw.com

Thornshaw Scientific Recruitment is a leading Irish provider of specialist Scientific Recruitment. Part of the CPL Group. www.thornshaw.com Tel: +353 1 2784671. 
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