Regulatory Affairs Specialist

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Dependant on Experience
Quanta Consultancy Services Ltd
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Are you looking for a step up into a senior position with a well known Medical Device company in Cork? 

I am currently recruiting for a Regulatory Affairs Specialist to work in a contract or permanent position (dependant on what candidate preference is). This is an excellent opportunity to develop your skills and work for a company with great career prospects!
Role Overview

As a Regulatory Affairs Specialist, you will be a key member of the Global Regulatory Affairs group. Within your role you will support site initiatives for all product continuous improvement projects, site to site transfers and design transfers.

You will develop regulatory strategies, along with preparing and supporting regulatory submissions for the sites range of Medical Devices. Other duties may include maintaining site Regulatory compliance.

Skills Required

To be considered for this position you must have a minimum of 3 years experience within a Regulatory Affairs position in Medical Devices.

You must have experience with full product lifecycle, change controls and ideally Class III Medical Devices.

You must have a degree in an Engineering or Science discipline and good planning and organisational abilities. Candidates should have the ability to work in diverse project teams and be able to communicate effectively with management and peers.

If this sounds like the job for you, please apply now and a representative will be in touch shortly!

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Contact Details:
Quanta Consultancy Services Ltd
Tel: (0) 1442 860 531
Contact: Xanthe Glaysher

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