Senior Regulatory Affairs Specialist, Medical Devices, Medical Device, Crawley, Senior Regulatory Affairs Specialist

This organisation is has been established for over 30 years and is a global market leader in developing and manufacturing oncology equipment used to diagnose cancer within the healthcare industry. Due to recent expansion, they now have a fantastic opportunity available for a Senior Regulatory Affairs Specialist to join their team in West Sussex.

As the Senior Regulatory Affairs Executive, you will be responsible for ensuring global compliance with regulatory standards for medical devices.

This role will include:
-Providing Regulatory submissions
-Providing Quality Assurance support
-Conducting GMP audits
-Advising the company of changes to quality and regulatory standards

The suitable candidate will ideally be educated to a Degree Level (or equivalent) within an Engineering discipline. Experience of leading a regulatory team within a medical device organisation is essential for this role. A strong background in working to ISO 13485, FDA and GMP standards is essential for this role.

The successful candidate will receive ongoing training and development to further enhance their skills.

Keywords – Regulatory Affairs Manager, Regulatory Affairs, Medical Devices, Medical Device, West Sussex, Crawley, Ra Manager, RA Specialist, Regulatory Affairs Specialist

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