QA Chemical Engineering Jobs | Apply Now For The Team Member Role at Dr. Reddy’s LaboratoriesÂ
Join Dr. Reddy’s Laboratories in Hyderabad as a team member in Quality Assurance and contribute to delivering high-quality, affordable, and innovative medicines to millions worldwide. This role offers an opportunity to work in a dynamic, globally recognized pharmaceutical company known for its scientific excellence, sustainability, and commitment to employee growth.
- Job Position: Team Member – Quality Assurance
- Location: Hyderabad, Telangana, India
About the Company
Dr. Reddy’s Laboratories is a leading multinational pharmaceutical company headquartered in India with a presence in 66 countries. Founded in 1984, the company has over 24,000 employees working towards the mission of accelerating access to affordable and innovative medicines—because good health can’t wait. Dr. Reddy’s is known for its strong focus on deep science, progressive people practices, robust corporate governance, and sustainability. It is recognized as a purpose-driven, future-ready, and equal opportunity employer, fostering diversity, equity, and inclusion across its global workforce.
Job Description
As a Team Member – Quality Assurance, you will be responsible for reviewing and approving analytical test data from the Quality Control department, ensuring compliance with cGMP/cGLP, and supporting continuous improvement of quality systems. You will collaborate with cross-functional teams, oversee data integrity, manage incidents and deviations, and ensure all quality processes meet regulatory and organizational standards.
Key Responsibilities
- Review and approve all analytical test data of Quality Control.
- Review and usage decision of analytical reports in LIMS, Empower, and SAP.
- Approve electronic signatures (level-2) for chromatography data station (CDS) and standalone instruments.
- Review analytical test reports in LIMS and report 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, including investigations, CAPA follow-up, and closure.
- Monitor analytical activities in the QC laboratory.
- Verify specifications, standard test procedures, worksheets, and analytical reports before approval.
- Review and verify audit trails for standalone, Empower, and LIMS systems.
- Ensure cGMP/cGLP compliance.
- Review and approve Excel sheet validations.
- Review results acceptance for API, excipients, and packing materials.
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Review compiled stability data, verify exhibit batch sampling protocols.
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Handle Robotic Process Automation of Chromatography Data review (RPACD).
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Perform any other tasks assigned by the reporting staff.
Qualifications
- Bachelor’s or Master’s degree in Pharmacy, Chemistry, Chemical Engineering, or related field.
- 3 to 7 years of experience in QC or AQA departments is mandatory.
- Strong knowledge of pharmaceutical quality systems, analytical review, and cGMP/cGLP compliance.
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