Associate Regulatory Affairs

Dr Reddy's Laboratories Limited

22 days ago

Princeton, NJ

Onsite

Full Time

Medior

0 applicants

View Job Listing

Apply to 100+ jobs

About this role

This role involves maintaining regulatory documentation, supporting review of CMC documents, coordinating with stakeholders, and assisting with regulatory submissions for pharmaceutical products. The position requires experience in regulatory affairs related to ANDA and post-approval processes, with a focus on collaboration, documentation, and agency communication.

Skills

Qualifications

Degree in Pharma3-5 Years Regulatory Experience

About Dr Reddy's Laboratories Limited

drreddys.com

Dr. Reddy’s Laboratories is an Indian multinational pharmaceutical company committed to the credo “Good Health Can’t Wait,” focused on accelerating access to affordable and innovative medicines. It develops, manufactures and markets a broad portfolio including generics, active pharmaceutical ingredients (APIs), biosimilars, consumer health products and novel therapeutics. The company pairs global manufacturing and regulatory capabilities with R&D programs and strategic partnerships to bring new and lower-cost treatments to market. Dr. Reddy’s also runs patient and healthcare-professional programs and emphasizes sustainability and access as core parts of its mission.