Department: Regulatory Affairs Designation: DRA Executive Location: Baddi / Chandigarh Reporting To: Regulatory Affairs Manager / Head – Regulatory Affairs DRA Executive We are looking for a qualified DRA Executive to support Drug Regulatory Affairs and compliance activities for pharmaceutical products. The position is based in Baddi / Chandigarh and involves regulatory documentation, dossier review, product approvals, artwork verification, MRP verification, and dispatch compliance. Job Purpose To support regulatory and compliance activities for pharmaceutical products, including regulatory documentation, artwork review, product approvals, MRP verification, and dispatch compliance. Key Responsibilities Review and maintain regulatory dossiers to ensure documents are complete, accurate, updated, and aligned with approved product details. Review manufacturing documents, specifications, COA, stability data, validation documents, licenses, approvals, CPP/COPP, and other applicable regulatory documents. Coordinate with QA, QC, Production, Artwork, Commercial, and other departments Qualification & Experience • Education: B.Pharm / M.Pharm • Experience: 2–3 years of experience in Drug Regulatory Affairs within the pharmaceutical industry. • Experience in regulatory documentation, artwork review, product approvals, and compliance will be preferred. Key Skills • Regulatory Documentation • Dossier Management • Artwork Review • Product Approvals • MRP & Pricing Compliance • Pharmaceutical Regulatory Compliance • Cross-functional Coordination Apply here linkedin