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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 (phone number removed) in all correspondence.
Please note:
This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
