Assist in the preparation and submission of regulatory documents to health authorities (e.g., FDA, EMA, CDSCO).
Support in maintaining regulatory databases, tracking submissions, and approvals.
Ensure compliance with applicable regulations, guidelines, and company SOPs.
Help prepare product registration dossiers, variations, renewals, and post-approval documentation.
Coordinate with cross-functional teams (R&D, QA, QC, manufacturing) to gather required data.
Assist in responding to queries from regulatory authorities.
Keep updated with changes in global regulatory guidelines and requirements.
Job Types: Full-time, Permanent, Fresher
Pay: ₹20,779.74 - ₹42,875.55 per month
Benefits:
Health insurance
Paid sick time
Provident Fund
Work Location: In person
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