Senior Regulatory Affairs Specialist / Remote/Hybrid (UK) / £50–£60 per hour
Contract: 12 months
Start: ASAP

We’re partnering with a global Life Sciences leader to hire an experienced Senior Regulatory Affairs Specialist - EMEA Product Registrations to support IVD and Medical Device registrations across the EMEA region. This role is ideal for someone confident in multi‑country registration management, regulatory strategy, and working with both authorities and distributors.
Key Responsibilities:

• Lead product and establishment registrations across EMEA.
• Develop and deliver registration strategies.
• Maintain regulatory records and databases.
• Support change control assessments, vigilance activities and re‑registrations.

Requirements:

• 8–10 years’ Regulatory Affairs experience in IVD/Medical Devices.
• Strong understanding of ISO 13485 and European/EMEA regulatory frameworks.
• Proven experience managing multi‑country registrations.
• Excellent communication and stakeholder management skills.

Ready for your next step?
Apply today to take on a high‑impact regional regulatory role.