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

Apply now or get in touch to learn more!