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© All Rights Reserved. ApplyBlast.com
Dr Reddy's Laboratories Limited
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.
Headquarters
Banjara Hills, Telangana, India
Company Size
10001+ employees
Founded
1984
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.
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
View leadership team, funding history,
and employee contacts for Dr Reddy's Laboratories Limited.
9% above the average for this role
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