Life Science QA Job at Dr Reddy’s
A rare chance has emerged for candidates seeking a Life Science QA Job at Dr Reddy’s Laboratories in Baddi, Himachal Pradesh. This opportunity is ideal for MSc Biotech, Microbiology, and Biochemistry graduates eager to advance their careers in the pharmaceutical industry.
About Dr Reddy’s Laboratories
Dr Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company operating in the healthcare sector. With a commitment to accelerating access to affordable and innovative medicines, the organisation has a presence in 66 countries and employs over 24,000 individuals. Established in 1984, Dr Reddy’s focuses on sustainability and corporate governance, aiming to reach over 1.5 billion patients worldwide by 2030. The company values diversity and maintains an inclusive work environment, ensuring equal opportunities for all employees.
Job Details
- Position: Team Member – Analytical QA
- Location: Baddi, Himachal Pradesh, India
Job Summary
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.
Job Description
The Quality Assurance Specialist at Dr. Reddy’s will play a crucial role in maintaining compliance within the QC laboratory. Responsibilities include participating in investigations of Quality Management System (QMS) documents, preparing trending reports for laboratory incidents, evaluating Change Controls, and reviewing analytical data for accuracy and compliance. The specialist will also oversee instrument calibration records and ensure adherence to Good Manufacturing Practices (GMP).
Key Responsibilities
- Participate in investigations of QMS documents such as OOS, OOT, and laboratory deviations.
- Prepare trending reports for OOS, OOT, and laboratory incidents, supporting CAPA identification.
- Evaluate Change Controls and CAPA action plans for effectiveness.
- Review all analytical data generated in the Quality Control laboratory.
- Ensure reliability and data integrity through instrument and equipment calibration records.
- Prepare and review documentation related to stability samples.
- Perform SAP transactions related to laboratory workflows and data entries.
- Review and approve method validation and transfer protocols.
Eligibility Criteria
Educational Qualification
- Graduation in Chemistry/Analytical Chemistry or Pharmacy is mandatory.
- A Master’s degree in Microbiology, Biochemistry, or Biotechnology is preferred. Additional certifications such as CQA, CPGP, or Six Sigma are advantageous.
Minimum Work Experience: 2+ years experience in a relevant field.
Required Skills
- Regulatory Compliance
- Technical Documentation
- Change Control
- Laboratory Information Management
- Risk Management
- Chromatography
- Good Manufacturing Practices (cGMP)
- Quality Management Systems (QMS)
Why Join Dr Reddy’s Laboratories?
Dr Reddy’s Laboratories actively supports career growth and professional development through personalized learning programs. The organization offers benefits that meet industry standards, including medical coverage, family support, and opportunities for continuous learning. By joining Dr Reddy’s, employees become part of a mission-driven organization that values integrity, diversity, and innovation in the pharmaceutical sector.
Conclusion
The Life Science QA Job at Dr Reddy’s Laboratories presents a compelling opportunity for qualified candidates in the life sciences field. With a focus on regulatory compliance and a commitment to innovation, Dr. Reddy’s is positioned to support the professional growth of its employees. Interested candidates are encouraged to apply for this Life Science QA Job at the earliest.
