Job Description
<p>The Assistant Manager - Regulatory Affairs will play a key role in ensuring compliance with global pharmaceutical regulations and supporting product registrations across multiple geographies. The role involves preparing, reviewing, and submitting regulatory dossiers, maintaining compliance with evolving regulatory requirements, and collaborating with cross- functional teams to ensure timely approvals.<br/><br/>This position offers exposure to global regulatory frameworks, product lifecycle management, and strategic interactions with health authorities, making it a critical role in driving compliance and market access.<br/><br/><b>Areas of Responsibility:</b><br/><br/>- Prepare, review, and submit regulatory dossiers (CTD/eCTD) for product approvals and renewals.<br/><br/>- Ensure compliance with global regulatory guidelines (FDA, EMA, CDSCO, WHO, MHRA, etc.).<br/><br/>- Support clinical trial applications,...
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