I'm looking for an experienced Regulatory Affairs professional to support EU/UK submissions, ensure compliance, and help drive regulatory strategy across our product portfolio.
What You’ll Do
- Manage regulatory submissions and lifecycle activities
- Review CTD documents and liaise with Health Authorities
- Ensure compliance of marketing authorisations
- Support and mentor junior team members
Job requirements
- BSc in Life Sciences, Pharmacy, or Chemistry
- 5+ years in pharmaceutical regulatory affairs
- Strong knowledge of EU/UK regulations and CTD
- CMC experience is desired but not essential
- Excellent communication and organisational skills
