Related skills
regulatory affairs eu regulations regulatory submissions cmc cis regulations📋 Description
- Oversee new product registrations and post-approval submissions.
- Review and write CMC modules 2 and 3.
- Coordinate regulatory filings for EU and CIS regions.
- Maintain regulatory processes and tracking tools.
- Foster relationships with health authorities and support launches.
- Develop and execute regulatory strategies aligned with the business plan.
🎯 Requirements
- Bachelor’s or Master’s in Life Science/Pharma.
- 4–6 years of relevant experience.
- RAPS certification desirable.
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