Dr Reddy’s Laboratories Hiring for Analytical QA Role | Pharma QA Job | Apply Now
Looking for a rewarding Pharma QA Job opportunity in the pharmaceutical industry? Dr. Reddy’s Laboratories is hiring for the position of Team Member – Analytical Quality Assurance through its latest Dr Reddy’s Careers hiring initiative. This opportunity is ideal for candidates experienced in QA/QC laboratory compliance, analytical data integrity, GMP, GLP, regulatory compliance, and Quality Management Systems. Candidates with qualifications in Pharmacy can apply for this exciting pharmaceutical career opportunity.
- Job Position: Team Member – Analytical Quality Assurance
- Location: India
About the Company
Dr Reddy’s Laboratories is a globally recognised pharmaceutical company operating across 66 countries with over 24,000 employees worldwide. Through Dr Reddy’s Careers, the company provides excellent opportunities for professionals seeking growth in Quality Assurance, Regulatory Affairs, Quality Control, Research, and manufacturing operations.
Founded in 1984, the company focuses on affordable and innovative healthcare solutions while maintaining sustainability, integrity, and strong corporate governance.
Job Description
This role is for a Quality Assurance Specialist – Analytical Compliance, responsible for ensuring end-to-end adherence to regulatory standards and SOPs in Quality Control (QC) laboratory operations, with a focus on analytical data integrity, investigation management, and documentation oversight.
Key Responsibilities
QMS & Compliance Responsibilities
- Participate in investigations related to OOS, OOT, and laboratory deviations.
- Ensure timely closure of QMS documents as per SOP timelines.
- Prepare trending reports and support CAPA implementation.
Analytical QA & Data Integrity Responsibilities
- Review analytical laboratory data, electronic records, and raw data for compliance.
- Review audit trails, calibration records, and GMP documentation.
- Verify compliance of GxP computer systems and laboratory operations.
Documentation & Laboratory Management
- Prepare and review stability sample documentation.
- Manage SAP transactions and QMS notifications through DCMS.
- Review method validation, method transfer protocols, and LIMS updates.
- Monitor cGLP practices in Quality Control and Microbiology laboratories.
Qualifications
- Educational qualification: A graduation in Pharmacy is mandatory. A Master’s in Pharmacy is preferred.
- Minimum work experience: 2-4 years of experience
Skills & Attributes & Critical Exposures
Functional Skills
- Regulatory Compliance
- Regulatory Filings
- Technical Documentation
- Change Control
- Laboratory Information
- Risk Management
- Chromatography
Resident Skills
- Product Quality (QA/QC)
- Current Good Manufacturing Practices (cGMPS)
- Good Laboratory Practice (GLP)
- Quality Management Systems (QMS)
Behavioural Skills
- Accuracy & Discipline – Upholds rigorous documentation and testing standards to ensure error-free, compliant results.
- Ownership – Proactively identifies risks, supports investigations, and maintains equipment readiness with accountability.
- Continuous Learning – Shares knowledge with new joiners, troubleshoots effectively, and contributes to laboratory excellence.
Critical exposures
- Experience with GMP, GLP, and global regulatory standards.
- Exposure to HPLC, GC, FTIR, and UV-Vis analytical techniques.
- Understanding of 21 CFR Part 11 and Annex 11 data integrity requirements.
- Experience handling OOS investigations and non-conformances.
- Knowledge of LC-MS, ICP-MS, and NMR instrumentation is preferred.
Benefits Offered
Employees at Dr Reddy’s Laboratories receive:
- Learning & development opportunities
- Career growth support
- Family medical coverage
- Life insurance benefits
- Maternity & Paternity support
- Relocation and joining assistance
