Warning: This vacancy expired on 19th Sep 2008.

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Job Description

Regulatory Affairs, Medical Devices, Medical Device, Regulatory Affairs Specialist, Bedfordshire.

This company specialises in developing, manufacturing and supplying fertility diagnostic products for the healthcare market. Although this company has not been established for long, they have already become a market leader within the medical device sector and are looking for a Regulatory Affairs Specialist to join the team in Bedfordshire.

As the Regulatory Affairs Specialist you will be responsible for providing regulatory support for the international distribution of the Diagnostic products.

Duties within this role will include:
*Processing regulatory enquiries from distribution companies and providing responses as required, including the acquisition of Certificates of Free Sale, and other legalised documents as required
*Preparing and maintaining marketing authorisation applications on a worldwide basis
*Maintaining the notifications to the EU Competent Authorities for CE marked products under (98/79/EC) and (93/42/EC) medical device directive
*Making and maintaining the required establishment registration and list applications to US FDA
*Reviewing all associated documentation

The suitable candidate will ideally be educated to a Degree level (or equivalent) within a Chemical/Biological discipline and have relevant experience of working within a Regulatory Affairs or Quality Assurance position within a medical device organisation. A strong understanding of ISO 13485, GMP and FDA standards is essential for this role.

The successful candidate will receive a competitive salary and full benefits package plus a fantastic work environment.

Paramount Recruitment Limited provides services as an agency and an employment business. We regularly have similar roles in this area. Please see our website for details or send your CV in to us to find out the latest opportunities.

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