Quality Assurance Jobs at Dr. Reddys Laboratories | Apply Now For The Team Member Role
Dr. Reddy’s Laboratories is seeking a skilled Team Member – Analytical Quality Assurance to join its Global Manufacturing Organisation in Hyderabad. This role offers the opportunity to contribute to world-class pharmaceutical quality standards, ensuring compliance, accuracy, and continuous innovation in analytical processes.
- Job Position: Team Member – Analytical Quality Assurance
- Location: Hyderabad, Telangana, India
About the Company
Dr. Reddy’s Laboratories is a leading multinational pharmaceutical company with a mission to accelerate access to affordable and innovative medicines — because Good Health Can’t Wait. Established in 1984, it now operates across 66 countries with 24,000+ employees. Driven by the purpose of sustainability, innovation, and excellence, Dr. Reddy’s delivers complex APIs and formulations through state-of-the-art manufacturing plants worldwide. The company fosters an inclusive, diverse, and dynamic workplace culture while ensuring ethical governance and environmental responsibility.
Job Description
As a Team Member in Analytical Quality Assurance (AQA), you will be responsible for reviewing, approving, and monitoring all analytical data and documentation in the Quality Control (QC) laboratory. This role demands high attention to detail, adherence to cGMP/cGLP standards, and effective cross-functional collaboration to ensure product quality, data integrity
, and compliance.Key Responsibilities
- Review and approve all analytical test data of Quality Control.
- Review analytical reports in LIMS, Empower, and SAP, and make usage decisions.
- Provide electronic level-2 signatures for Chromatography Data Station (CDS) and standalone instruments.
- Review reported results against specifications and trends.
- Review method validation and method transfer documents.
- Review instrument calibrations and working standard qualification records.
- Handle incidents/deviations, out-of-trends, out-of-specifications, investigations, CAPA follow-up, and closure.
- Monitor analytical activities in QC labs and verify specifications, STPs, worksheets, and reports.
- Review audit trails for Standalone, Empower, and LIMS.
- Ensure cGMP/cGLP compliance and adherence to Safety, Health, and Environmental practices.
- Review and approve excel sheet validations.
- Review results for API, excipients, and packing material.
- Compile, review, and verify stability data and exhibit batch sampling protocols.
- Handle robotic process automation of chromatography data review (RPACD).
- Perform any other activities assigned by the reporting manager.
Qualifications
- Bachelor’s/Master’s degree in Pharmacy, Chemistry, Chemical Engineering, or a related field.
- 3–7 years of experience in QC or AQA department (mandatory).
- Strong knowledge of cGMP/cGLP, analytical review systems (LIMS, Empower, SAP).
- Excellent analytical, documentation, and communication skills.
- Ability to handle deviations, OOS/OOT investigations, and CAPA.
- Detail-oriented and capable of managing multiple priorities effectively.
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