EU Regulatory Change Leader - CMC & RA Expert
Clinical Role Overview
Thermo Fisher Scientific seeks an experienced Regulatory Affairs professional to support EU/EEA regulatory assessments of changes for clinical trial documentation and related CMC activities. The role focuses on coordinating regulatory change control, SoC preparation and interaction with cross-functional teams.
The candidate will review SmPCs, labels, manufacturing licences and GMP certificates, providing regulatory intelligence and expert review of CMC documentation as needed.
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Key Details
- Date Posted: 23 Oct 2026
- Location: milano
- Employment Type: Permanent
- Workplace: On-site
- Category: General
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ThermoFisher Scientific
Verified Healthcare EmployerVerified NHS trust or certified UK healthcare facility offering professional development and clinical governance.
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