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Salary:
45.00 - 62.93 per hour PAYE or 65.00 - 84.55 per hour Umbrella.
CMC Regulatory Affairs Consultant Role:
- Responsible for the development of CMC/technical regulatory strategies across the EMEA.
- Leads a Regulatory Affairs team ensuring the success of new product registrations, line extensions and new indications and claims.
- Manages the global or regional regulatory deliverables for drugs, dietary supplements & medical devices as relevant.
- Develops strong partnerships with Regulatory Affairs Franchise, R&D, Marketing, Supply Chain & local business representatives.
- Represents the Regulatory Affairs CMC function as appropriate in Self Care Franchise, functional & business Leadership teams.
Your Background:
- Relevant Bachelor's Degree or equivalent work experience inpharmaceutical CMC regulatory affairs.
- Expertise across a broad spectrum of Regulatory classifications including Drugs, Dietary Supplement and/or Medical Devices.
- Knowledge of regulatory frameworks and external environments in the EU/EMEA , & the ability to apply these to regulatory solutions throughout the product lifecycle.
- Solid understanding of regulatory CMC in the markets of relevance.
- Strong project management skills.
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. This is a hybrid role with 2-3 days expected on site.
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference (Apply online only).
Please note:
This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
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