Dr. Reddy’s Laboratories is Hiring Team Member – Quality Control in Hyderabad

A rare chance has emerged at Dr. Reddy’s Laboratories for aspiring Quality Control professionals. This opening is listed under Dr Reddy’s Laboratories careers and is based in Hyderabad, Telangana, India, inviting qualified candidates to apply for the position of Team Member – Quality Control.

About Dr. Reddy’s Laboratories

Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company with a presence in various global locations. With over 24,000 employees, the organization is dedicated to accelerating access to affordable and innovative medicines, embodying the belief that

Good Health Can’t Wait.: Established in 1984, Dr. Reddy’s has expanded its operations to include research and development centers, manufacturing facilities, and a commercial presence across 66 countries.

Dr Reddy’s Laboratories Careers: Job Details

Position: Team Member – Quality Control

Location: Hyderabad, Telangana, India

Job Description

The Quality Control Analyst will be responsible for performing analysis of raw materials, in-process samples, finished products, and stability samples in compliance with approved specifications, SOPs, and regulatory requirements (cGMP, USFDA, ICH). This Dr. Reddy’s Quality Control role involves handling analytical instruments, ensuring data integrity, and maintaining documentation as per audit standards.

Key Responsibilities

• Perform analysis of API, excipients, in-process, finished products, and stability samples.
• Execute testing using instruments such as HPLC, GC, UV-Visible Spectrophotometer, Dissolution, KF, IR, etc.
• Ensure adherence to approved STPs, specifications, and SOPs.
• Operate and maintain analytical instruments like HPLC, GC, Dissolution apparatus, FTIR, KF, etc.
• Perform routine checks, system suitability, and troubleshooting.

Eligibility Criteria

• M.Sc (Chemistry) or B.Pharm.

Required Skills

• Strong knowledge of analytical techniques (HPLC, GC, etc.).
• Good understanding of cGMP, data integrity, and regulatory expectations.
• Familiarity with LIMS and electronic data management systems.
• Good documentation and communication skills.
• Experience in Empower and LIMS software.

Additional Information

• Record all raw data in notebooks / LIMS systems as per ALCOA+ principles.
• Ensure proper documentation with no overwriting, no loose sheets, and traceability.
• Review analytical data for accuracy and compliance.
• Follow cGMP, GLP, Data Integrity (DI), and regulatory guidelines.
• Assist in OOS, OOT, deviation, and incident investigations.
• Support root cause analysis and implementation of CAPA.
• Perform stability sample analysis and trending.
• Ensure timely completion of assigned samples.

How to Apply

Interested candidates can apply through the following link: CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE

Conclusion

This opportunity at Dr. Reddy’s Laboratories represents a significant step for qualified candidates aiming to advance their careers in Quality Control. For candidates exploring Dr Reddy’s Laboratories careers, interested individuals are encouraged to apply before the deadline to be considered for this role.