Your new company

This company is looking for a Regulatory Affairs Associate/Officer role. They are a well established generic business.

Your new role

With a focus on post-approval activities, the successful candidate will have exposure to many aspects of regulatory compliance as well as the opportunity to supervise and guide a team. This role you will be based on-site in the reading area.

What you'll need to succeed

Participate in the review of process/product changes, deviations, product complaints, adverse drug reactions, medical information, and batch recall to determine the need for any regulatory activities and to ensure compliance with regulatory requirements. You will need 1–2 years of Regulatory Affairs experience. Strong understanding of the current UK and European regulations, laws, guidelines, and industry requirements. Experience with generic products and MRP/DCP submissions is advantageous.

What you'll get in return

You will get the opportunity to have great exposure and grow your regulatory affairs team.

What you need to do now

george.costard1@hays.com

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

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