At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.
Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.”
Job Summary:
- Strong knowledge of USFDA, ICH guidelines, regional regulations (US, EU, India), and submission formats.
- Prepare, compile, and submit regulatory dossiers (e.g., CTD/eCTD) for new drug applications (NDAs), ANDAs, MAAs, and post-approval changes
- Support regulatory strategy development for new products and markets
- Coordinate with cross-functional teams (CDMO, R&D, Manufacturing) to gather required documentation and data.
- Respond to queries and deficiency letters from regulatory authorities
- Maintain regulatory databases and track submission timelines and approvals
