Regulatory Affairs Manager UK and Ireland
JOB_53908274792787Job type
ContractLocation
Cambridge / RemoteWorking Pattern
Full-timeSpecialism
Life Sciences ManufacturingIndustry
Scientific and R&DPay
Inside IR35Closing date
30 Jun 2026
Regulatory Affairs Manager Conract– UK & Ireland Affiliate
Your new company
You’ll be joining a leading, research‑driven biopharmaceutical organisation with a strong UK & Ireland presence and large global footprint. The business manages a robust portfolio of centrally approved medicines and continues to invest in regulatory capability to support post‑approval lifecycle management and commercial growth across the UK&I markets.
Your new role
- Post‑approval lifecycle management (LCM) activities for UK & Ireland
- Management of complex Type II and other significant variations
- Regulatory support for Paediatric Investigation Plans (PIPs)
- Involvement in clinical trial regulatory activities
- Review and approval of promotional and non‑promotional materials
- Use of Veeva regulatory information management systems
What you'll need to succeed
- Demonstrated experience with complex variations, including Type II
- Proven experience in UK & Ireland affiliate regulatory affairs
- Strong post‑MAA lifecycle management expertise for CP products
- Exposure to PIPs and clinical trial regulatory submissions
- Experience working with Veeva or similar regulatory systems
- Excellent communication skills and confidence working cross-functional
- A collaborative, hands-on approach with a willingness to support across the wider team
What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you, but you are looking for a new position, please contact Julia Bowden for a confidential discussion about your career.
Talk to Julia Bowden, the specialist consultant managing this position
Located in London-City, 5th Floor, 107 Cheapside, Telephone +443330106057