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CMC Regulatory Affairs Consultant, High Wycombe
Client: CK Group
Location: High Wycombe, United Kingdom
Job Category: Other
EU work permit required: Yes
Job Views:
4
Posted:
28.04.2025
Expiry Date:
12.06.2025
Job Description:
CK Group is recruiting for a CMC Regulatory Affairs Consultant to join a pharmaceutical company at their site in High Wycombe on a 6-month contract.
Salary: £45-£62.93 per hour PAYE or £65-£84.55 per hour Umbrella
Role:
* Responsible for developing CMC/technical regulatory strategies across the EMEA.
* Leads a Regulatory Affairs team to ensure success in new product registrations, line extensions, and new indications and claims.
* Manages global or regional regulatory deliverables for drugs, dietary supplements, and medical devices as relevant.
* Develops strong partnerships with Regulatory Affairs Franchise, R&D, Marketing, Supply Chain, and local business representatives.
* Represents the Regulatory Affairs CMC function in the Self Care Franchise, and in functional & business leadership teams.
Your Background:
* Bachelor's Degree or equivalent experience in pharmaceutical CMC regulatory affairs.
* Experience across regulatory classifications including drugs, dietary supplements, and medical devices.
* Knowledge of EU/EMEA regulatory frameworks and ability to apply them throughout the product lifecycle.
* Strong understanding of regulatory CMC in relevant markets.
Company:
The client is a leading healthcare company dedicated to improving access, affordability, and creating healthier communities worldwide.
Location:
This role is based at the client's site in High Wycombe, with a hybrid work model of 2-3 days on-site per week.
Apply:
For more information or to apply, contact the Key Accounts Team at 01438 870011 or email [emailprotected]. Please quote reference 132 033. It is essential that applicants hold entitlement to work in the UK.
Note: This role may require a satisfactory DBS check.
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