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Regulatory Affairs

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Regulatory Affairs

Regulatory affairs specialists are in constant demand throughout the life sciences industry, whether for trialing new drugs and devices, bringing them to market or maintaining their licenses.

We specialise in finding professionals with the specific experience and skill sets that match our clients’ regulatory requirements. Our dedicated RA team works across the pharmaceutical, biotech and medical devices sectors, providing specialist staff for clinical trial applications, marketing applications (MRP, DCP, CP) through to life cycle management, CMC, labelling and artwork, regulatory operations, CE marking and 510K.

Our RA team has an exceptionally strong network of high-quality candidates across the regulatory arena, many of who choose to work with us exclusively and can't be easily found by other recruiters.

Contact us to find you the right regulatory affairs resources. Roles we place on a regular basis include:

  • Regulatory affairs officer/executive/advisor/associate
  • Senior regulatory affairs officer/executive/advisor/associate
  • Senior / regulatory affairs consultant
  • Regulatory affairs project manager
  • Regulatory affairs manager
  • QA/RA manager
  • Senior regulatory affairs manager
  • Associate regulatory affairs director
  • Head of regulatory affairs
  • Senior / regulatory affairs director
  • VP of regulatory affairs