Senior Associate – Regulatory Affairs (EU-OTC)

📋 Description

• Submission management for MRP, DCP, PSUSA, renewals and variations
• Support EU OTC drug registrations across countries
• Compile submission packages with regional RA team
• Prepare cover letters, forms and Module 1 docs for variations
• Prepare regulatory docs for registration, variation and renewal in EMEA
• Manage regulatory action item trackers and timing coordination