Manage all types of CMC changes and variations (minor, moderate, major) as per country-specific regulatory requirements.
Collaborate and communicate effectively with client teams and stakeholders for data, clarifications, and approvals.
Author and compile complete variation submission packages , ensuring accuracy and compliance.
Review compiled packages to verify alignment with source data and regional guidelines.
Work across all dosage forms , including solid oral, injectables, liquids, and others.
Handle submissions for EU, South Africa (SA), and Australia / New Zealand (ANZ) markets.
Required Skills :
Strong understanding of global CMC variation requirements.
Excellent documentation, communication, and coordination skills.
Attention to detail and ability to work with cross-functional teams.
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Regulatory Specialist • India
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