Walker Cole International is supporting a pharmaceutical company in the search for a Regulatory CMC Officer to join their growing Regulatory team in the UK.
This position will support regulatory lifecycle activities across a portfolio of specialty pharmaceutical products distributed across UK and European markets.
The role offers strong exposure to CMC regulatory activities, post-approval submissions, and international lifecycle management within a fast-paced and collaborative environment.
Key responsibilities
- Support regulatory lifecycle management activities across UK and European markets
- Prepare and submit CMC regulatory documentation, including variations and post-approval changes
- Coordinate regulatory submissions in line with MHRA and European regulatory requirements
- Maintain regulatory compliance for existing marketed products across multiple territories
- Work cross-functionally with Quality, Supply Chain, Medical Affairs, and commercial teams
- Support artwork and labelling updates where required
- Monitor regulatory changes and support implementation activities across the portfolio
About you
- 2–3 years of Regulatory Affairs experience within the pharmaceutical industry
- Strong exposure to CMC regulatory activities and lifecycle management
- Experience preparing and managing regulatory submissions and variations
- Understanding of UK and/or EU pharmaceutical regulatory frameworks
- Strong organisational skills with the ability to manage multiple projects simultaneously
- Comfortable working within a collaborative and evolving business environment
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