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Regulatory Affairs Executive - Med Dev - UK

Business Type: Medical Devices Company
Job Type: Quality Assurance - Control, Audit, Project Management, Regulatory Affairs, Compliance
Job Level: Experienced (non manager)
Position: Full Time
Salary: GBP25000 per annum + benefits
Location: North West
Reference: AB-RAA-1
Closing Date: 18/08/12

At Associate level, the tasks will be primarily support work in the first term, but with good scope for long term career development

    • Contributing to regulatory and quality project teams
    • Reviewing technical data as part of a project team
    • Providing regulatory review and technical input
    • Providing quality review and input
    • Building and maintaining exceptional client relationships

A good base for thsi role would be a Degree in the Life Science together with around 2 years Regulatory Affairs experience. Product Life Cycle Management is essential with a good knowledge of the UK /EU regulations and guidelines, CMC experience of EU, DCP, MRP, CP applications and variations. Experience of eCTD would also be beneficial.

For more information on this vacancy, or any other medical device opportunities, please contact the Senior Consultant Andrew Boroky on 0044 (0) 207 940 2116, or email him at

Posted: 11/08/2012 | NPJ Ref: 84895
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