My client is a world leader in specialty generic injectable pharmaceuticals; they offer one of the broadest portfolios of generic acute-care and oncology injectables, as well as integrated infusion therapy and medication management solutions.

They are currently recruiting for 3 x Senior Regulatory Affairs Associates to work on 12-18 month contracts in their offices in Warwickshire. Primary responsibilities of the role will be to assemble and publish regulatory dossiers, in both paper and electronic formats and submit these to the Health Authorities.

You the successful candidate will be educated to degree level and have extensive Regulatory Affairs Experience. You will be able to demonstrate a strong understanding of dossier authoring and publishing (paper and electronic) and implementation of process improvements. Excellent communication and interpersonal skills are also required for this position.

In return an excellent salary and package are on offer.

To discuss this role and similar opportunities, please call Russ Broome on 0845 883 0000

If you have not heard back within 7 days, please assume your application has been unsuccessful

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