At a Glance
- Tasks: Lead regulatory direction for medical devices from concept to launch across multiple regions.
- Company: Join CooperVision, a leader in the medical devices industry.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Collaborative environment with opportunities to work across diverse regions.
- Why this job: Make a significant impact on healthcare by ensuring compliance and safety of innovative products.
- Qualifications: Strong technical writing skills and experience in regulatory affairs are essential.
The predicted salary is between 60000 - 80000 £ per year.
Cooper Vision is seeking a Principal Regulatory Affairs Specialist to lead regulatory direction across the UKI, Be Ne Lux and Nordic clusters, from concept to launch and post market.
You will manage submissions, maintain regulatory files, and interact with government bodies to ensure compliance with UK, EU, ACE and MENA requirements.
Strong technical writing and cross‑functional leadership are essential for this role. #J-18808-Ljbffr
We think you need these skills to ace EMEA Regulatory Affairs Lead – Medical Devices in Southampton
Regulatory Affairs
Technical Writing
Cross-Functional Leadership
Submission Management
Regulatory Compliance
Interaction with Government Bodies
Knowledge of UK Regulations
