Regulatory Executive

Key Responsibilities:

• Prepare, review and compile regulatory submission dossiers for new product registrations and renewals.
• Ensure compliance with national drug regulatory authority guidelines, packaging & labelling requirements, and pharma regulations.
• Maintain regulatory filings, track regulatory changes and proactively update internal teams on implications.
• Liaise with QA/RA, production, marketing and external regulatory agents/distributors as required.
• Support post-approval changes, variations, and ensure documentation is maintained and audit-ready.

Requirements:

• Pharm-D from a recognized institution.
• 2–5 years’ experience in regulatory affairs or business development in the pharmaceutical industry.
• Good understanding of regulatory submission formats (ACTD/CTD preferred) and life-cycle management.
• Strong organizational, analytical and communication skills; able to work with cross-functional teams.
• Proficient in MS Office (Word, Excel, PowerPoint) and able to maintain regulatory databases/tracking systems.

Job Type: Full-time

Application Question(s):

• Please mention your current monthly salary.
• What is your expected monthly salary for this position?
• How many years of relevant work experience do you have in related field?
• Where are you currently residing (city and area)?
• If selected, how soon can you join?

Work Location: In person