Your new company
Excellent opportunity to join an international company, leader in their sector, who is looking for a Quality Assurance / Regulatory Affairs Specialist in Medical Devices area.

Your new role
This professional will be responsible to ensure the correct application of the EU Medical Device Regulation 745/2017, and to maintain and continuously improve the local Quality Management System (QMS). This person will also be responsible for supporting inspections, executing internal audits and manage all the documentation, Change Controls, CAPAS and claims.

What you'll need to succeed
We are looking for a professional with a Degree in Life Sciences and at least 5 years of experience in similar roles. Good knowledge of ISO 9001 and ISO 13485 is desired. Good English skills, both spoken and written are mandatory. This person has to be a good communicator, confident, resilient and with the ability to influence others.

What you'll get in return
This is an excellent opportunity to join a company where the human resources are valued.

What you need to know
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV. If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.
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