Dr Reddy's Laboratories Limited
This role involves reviewing and approving qualification protocols, validation master plans, and related documentation for facilities, equipment, and utilities within a pharmaceutical manufacturing environment. The position requires ensuring compliance with quality standards, managing quality management system activities, and participating in investigations for incidents or deviations. The ideal candidate will leverage their experience to maintain rigorous quality assurance practices and support operational excellence.
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
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