Regulatory Affairs Specialist, Medical Devices, Medical Device, Bedford, Regulatory Affairs Specialist

This company is a specialist developing and manufacturing medical diagnostics for hospitals, clinics and laboratories world wide. Due to an increase in the work load they now have an exciting opportunity for a 12 months fixed term contract Regulatory Affairs Specialist based in Bedford.
As the Contract Regulatory Affairs Specialist you will be responsible for maintaining product specific technical files. This role will also involve reviewing product instruction leaflets, labeling and promotional material. Maintaining the SAP regulatory control mechanism will also be part of this varied role.

The suitable candidate will ideally be educated to a Degree level (or equivalent) within an engineering discipline. Experience of working to ISO 13485, FDA and GMP standards is required for this role. You will also have experience of working within a regulatory role in the medical devices industry.

Within this role you will have the opportunity to work for a globally recognised market leader.

Keywords – Regulatory Affairs Manager, Regulatory Affairs, Medical Devices, Medical Device, Bedford, Bedfordshire, Ra Manager, RA Specialist, Regulatory Affairs Specialist

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