Job Title:

Executive – Regulatory Affairs

Business Unit:

R&D1; Regulatory Affairs

Job Grade

G12A

Location:

Vadodara

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 team-oriented spirit, knowing that we ‘Thrive together’ and support each other’s journeys.”

Job Summary

Evaluation of regulatory documents, compilation of dossier and submissions to CDSCO-HQ for regulatory approval of drug substance and drug products.

Area of responsibility:

- Evaluation of regulatory strategies for products to be registered in India




- Review of CMC & other documents, coordination with cross functional teams for necessary corrections, preparation of cover letter of application & other regulatory documents, compilation of regulatory dossier and submission on the portal of regulatory authority for obtaining, CT, BE and domestic manufacturing and marketing permission Import & marketing approval in India Compilation of IPC testing dossier and coordination for sample readiness and submission to laboratory Post approval changes Phase IV CT applications Additional site notification/approval Condition compliance
- Checking artworks of product label and coordinate for necessary corrections

Preparation of prescribing information

Travel Estimate

NA

📌 Executive - IRA (India)
🏢 SUN PHARMA
📍 India