-end="189">Team Member Role for Analytical QA at Dr. Reddy’s | Chemistry Graduates Apply
Dr. Reddy’s Laboratories, a global leader in affordable and innovative medicines, is inviting applications for the role of Team Member – Analytical Quality Assurance at its Hyderabad facility. This opportunity is ideal for professionals with 3-7 years of experience in QC or AQA departments who are skilled in reviewing analytical test data, ensuring compliance with cGMP/cGLP, and supporting global pharmaceutical operations.
- Job Position: Team Member – Analytical Quality Assurance (AQA)
- Job Location: Hyderabad, Telangana, India
- Function / Department: Global Manufacturing Organisation (GMO)
About the Company:
Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company committed to ‘Good Health Can’t Wait.’ Established in 1984, the company operates in 66 countries, employing over 24,000 people. With 19 state-of-the-art manufacturing facilities and strong R&D capabilities, Dr. Reddy’s delivers high-quality generics, APIs, biosimilars, and specialty medicines across key therapeutic areas, focusing on access, innovation, and sustainability in the global healthcare landscape.
Qualifications:
Bachelor’s/Master’s degree in Chemistry, Chemical Engineering, or a related field
Experience
3–7 years of mandatory experience in the QC or AQA department
Job Description:
The Team Member – Analytical Quality Assurance will be responsible for reviewing and approving analytical data, ensuring compliance with cGMP/cGLP, and monitoring laboratory operations to support pharmaceutical quality and regulatory standards.
Analytical QA Job Role – Roles and Responsibilities:
- Review and approval of all analytical test data of Quality Control.
- Review and usage decision of analytical reports in LIMS, Empower, and SAP.
- Electronic signatures (Level-2) for chromatography data station (CDS) and standalone instruments.
- Review analytical test reports in LIMS and results against specifications and trends.
- Verify method validation, method transfer documents, instrument calibration, and working standard qualification records.
- Handle Incidents/Deviations, OOT, OOS investigations, and follow up on CAPA.
- Monitor analytical activities in QC laboratory.
- Verify and review audit trails in Empower, LIMS, and standalone systems.
- Ensure compliance with cGMP and cGLP practices.
- Review and approve Excel sheet validations.
- Review acceptance results for API, excipients, and packing materials.
- Review stability data and exhibit batch sampling protocols.
- Handle robotic process automation for chromatography data review (RPACD).
- Perform additional activities as assigned by reporting staff.
Analytical QA Job Role – Benefits Offered:
- Joining and relocation support
- Family support (Maternity & Paternity benefits)
- Medical coverage for employees and families
- Life insurance coverage
- Learning and development opportunities
- Professional growth through personalized training programs
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