Executive, Regulatory Affairs

Job Responsibilities:

• Coordinate with DGDA officials to facilitate regulatory processes, including product registration, renewal, price approval, and block list approvals.
• Maintain DGDA submission files, approval records and regulatory tracking reports.
• Coordinate with QA/QC, Production, R&D, and Marketing departments to support new product development and launch.
• Liaise with the Department of Narcotics Control for import and export permissions of controlled substances.

Requirements:

• B.Pharm/M.Pharm from a reputed university.
• 2-3 years of relevant experience in Drug Regulatory Affairs.
• Strong knowledge of DGDA guidelines, Drugs Act 1940/2023.
• Good communication and documentation skills.
• Proficiency in Microsoft Office

Compensation & Benefits:

Competitive salary package.

Extensive learning and development opportunities.

Structured career growth within a leading pharmaceutical organization.