Regulatory Affairs Consultant

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 24.00 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.
• Supports 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.
• Supports 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:

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.