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Regulatory Affairs Consultant

2 months ago


London, United Kingdom CK Group Full time
CK Group are recruiting for a Regulatory Affairs Consultant to join a company in the Pharmaceutical industry at their site based in High Wycombe, on a contract basis for 6 months.

Salary:
Up to £64.18 per hour PAYE or £86.00 per hour via umbrella. This role is inside IR35.

Regulatory Affairs Consultant Role:
  • Management of post-approval activities for specified OTC products.
  • Support the EMEA Regulatory Affairs team for post-approval activities for MRP/DCP products across EEA.
  • Coordinate worksharing (WS) procedures for CMC and non-CMC variation, when WS is appropriate.
  • Support the team with regional regulatory strategies in line with business plan for post-approval activities.
  • Ensure responses are submitted in a timely way in line with standard procedures and metrics.
  • May act as an ambassador for the Regulatory Affairs department to raise profile of team both internally and externally.

Your Background:
  • Hold a relevant degree in a life science or chemical subject.
  • Extensive working experience in the regulatory space, preferably with Over the Counter or FMCG.
  • Ability to work with minimal supervision to plan, conduct, and manage regulatory submissions for European.

Company:
Our client is the largest and most broadly-based healthcare company. They strive to improve access and affordability, create healthier communities, and put a healthy mind, body and environment within reach of everyone, everywhere.

Location:
This role is based at our clients site in High Wycombe.

Apply:
For more information or to apply for this Regulatory Affairs Consultant position, please contact the Key Accounts Team on or email .
It is essential that applicants hold entitlement to work in the UK. Please quote job reference 105158 in all correspondence.

Please note:
This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.