Hyderabad

Dr. Reddy's Laboratories is an Indian multinational pharmaceutical company located in Hyderabad, Telangana, India. The company was founded by Kallam Anji Reddy, who previously worked in the mentor institute Indian Drugs and Pharmaceuticals Limited.

NIAB invites applications for admission to its PhD program in Biotechnology from highly motivated students for the 2025-2026 Academic Session. The institute provides opportunities for pursuing cutting-edge research using advanced technologies in frontier areas of Animal Biotechnology.

The Clinical Research Lead will oversee and manage clinical research activities within the organization. This role involves designing, implementing, and monitoring clinical trials to ensure they meet regulatory requirements and organizational goals.

This is a non-supervisory position in Reference Standard Laboratory responsible for performing the required tests as part of the project and maintaining the GLP environment in the Laboratory. The incumbent will utilize his or her technical expertise, knowledge of pharmaceutical analysis in collaborative testing, efficient and effective laboratory operations.

R&D Data Steward plays a critical role in the intersection between business and data, where stewards will guide business teams on how to unlock value from data. This role will drive definition and documentation of R&D data standards in line with enterprise.

Collecting and submitting in-process samples, finished product samples, stability samples, control samples, cleaning samples, and other samples as per the respective procedures, batch manufacturing records and packing records, protocols. Conducting AQl inspections and periodic inspections of control samples

B.Pharmacy or Pharm.D. Age below 30 years. 2 years experience coordinating in clinical trials. Knowledge of MS Office suite; document scanning, uploading, email communication and database management.

Compression, Coating, Capsule Filling, FBP. QC Microbiology, IP/FP, Stability, GLP,RM. QA IPQA, AQA, APQR.

Familiarity with high-performance organizational tools and a strong understanding of digital manufacturing processes, computer system validation requirements, and quality management within biologics production and quality.