MSc Life Science Job at Dr. Reddy’s
Looking for a rewarding MSc Life Science Job in the pharmaceutical industry? Here’s an exciting opportunity from Dr. Reddy’s Laboratories that could accelerate your professional journey in analytical quality assurance. Dr. Reddy’s Careers is now hiring Team Members – Analytical Quality Assurance in Andhra Pradesh for candidates with expertise in microbiology, biotechnology, biochemistry, chemistry, and pharmacy. This role offers a fantastic opportunity for life science graduates to work with advanced analytical technologies, GMP systems, and global regulatory compliance in one of India’s leading pharmaceutical companies.
About Dr. Reddy’s Laboratories
Dr. Reddy’s Laboratories is a globally recognized pharmaceutical company headquartered in India with operations in more than 66 countries. Established in 1984, the organization focuses on affordable and innovative medicines while maintaining strong commitments toward sustainability, research, and patient care. Dr. Reddy’s Careers provide excellent opportunities for professionals in pharmaceutical sciences, biotechnology, microbiology, and analytical research.
Job Details:
- Job Title: Team Member – Analytical Quality Assurance
- Location: Andhra Pradesh
About the Role
The Team Member – Analytical Quality Assurance role is responsible for ensuring end-to-end compliance with regulatory requirements, Standard Operating Procedures (SOPs), and quality standards within Quality Control laboratory operations. The position focuses on analytical data integrity, investigation management, laboratory compliance, and documentation oversight to support reliable and compliant pharmaceutical manufacturing processes.
Key Responsibilities
- Participate in investigations related to Quality Management System (QMS) documents, including Out of Specification (OOS), Out of Trend (OOT), and laboratory deviations, ensuring timely closure in line with SOP requirements.
- Prepare trending reports for OOS, OOT, and laboratory incidents to support Corrective and Preventive Action (CAPA) identification and process improvements.
- Evaluate Change Controls and CAPA action plans to confirm root cause resolution and prevent recurrence.
- Review analytical data generated in the Quality Control laboratory, including electronic and raw data, to ensure accuracy, integrity, and compliance with SOPs.
- Review instrument calibration records and audit trails to verify equipment reliability, data integrity, and GMP compliance.
- Prepare and review stability sample documentation while ensuring proper maintenance of reference standards, impurity standards, working standards, and associated records.
- Perform and verify SAP transactions related to laboratory workflows and data entries to ensure traceability and compliance.
- Manage QMS notifications through DCMS systems.
- Monitor adherence to current Good Laboratory Practices (cGLP) across Quality Control and Microbiology laboratories.
- Verify audit trails for all GxP computer systems used within the Quality Control laboratory.
- Prepare, review, and approve stability study protocols on Laboratory Information Management Systems (LIMS).
- Review and approve method validation and method transfer protocols, reports, LIMS master data, and control limit updates to ensure analytical consistency across systems.
Required Qualifications
- Master’s Degree in Microbiology, Biochemistry, or Biotechnology is preferred.
- 2–4 years of relevant industry experience in Quality Assurance or Quality Control functions.
Functional Skills
- Regulatory Compliance and Regulatory Filings
- Technical Documentation
- Change Control Management
- Laboratory Information Systems
- Risk Management
- Chromatography Techniques
Core Competencies
- Product Quality Assurance and Quality Control (QA/QC)
- Current Good Manufacturing Practices (cGMP)
- Good Laboratory Practices (GLP)
- Quality Management Systems (QMS)
Behavioural Competencies
- Strong attention to detail and discipline in documentation and testing practices.
- Proactive ownership in identifying risks and supporting investigations.
- Continuous learning mindset with the ability to troubleshoot and share knowledge effectively.
Preferred Experience
- Experience ensuring compliance with GMP, GLP, and global regulatory standards.
- Exposure to analytical techniques such as HPLC, GC, FTIR, and UV-Vis.
- Knowledge of data integrity requirements including 21 CFR Part 11 and Annex 11.
- Experience investigating Out-of-Specification (OOS) results and non-conformances.
- Hands-on exposure to advanced analytical instruments such as LC-MS, ICP-MS, and NMR is an added advantage.
Benefits and Growth Opportunities
Dr. Reddy’s Laboratories offers career growth and professional development through personalized learning programs and industry-leading employee benefits, including relocation support, family support programs, medical coverage, life insurance, and continuous learning opportunities.
