Regulatory Affairs Officer
U S Pharma India · Mumbai · onsite · Posted today
Undisclosed2–3 yrsfulltimeSourced from
About a minute. You'll make an account on the way through.
About this role
Role & responsibilities :
- Prepare, compile, review, and submit regulatory dossiers (CTD/eCTD/ACTD) for product registration, renewal, and variation.
- Respond to regulatory authority queries within stipulated timelines.
- Review product labels, artworks, leaflets, and packaging to ensure regulatory compliance.
- Coordinate with internal departments such as QA, QC, Production, R&D, and Marketing.
Sourced from naukri
Skills
DossierRow MarketRegulatory AffairsEctdDossier PreparationCTD