Team Member – Analytical QA at Dr. Reddy’s Laboratories | Pharma Graduates Apply
A Dr Reddy Baddi vacancy for a Team Member in Analytical QA has emerged in Baddi, Himachal Pradesh. This opportunity is ideal for candidates with a background in Chemistry or Pharmacy, looking to contribute to a leading multinational pharmaceutical company.
About the Company
Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of the 24,000-plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait. The company has research and development centres, manufacturing facilities, and a commercial presence in 66 countries. Dr. Reddy’s is committed to sustainability and aims to reach over 1.5 billion patients worldwide by 2030.
Job Details: Dr Reddy Baddi Vacancy
- Company: Dr. Reddy’s Laboratories
- Position: Team Member – Analytical QA
- Location: Baddi, Himachal Pradesh, India
Job Description
For this Dr Reddy Baddi vacancy, the 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
- Participate in investigations of Quality Management System (QMS) documents such as OOS, OOT, and laboratory deviations, ensuring timely closures as per SOP timelines.
- Prepare trending reports for OOS, OOT, and laboratory incidents, using analytical insights to support CAPA identification and process improvements.
- Evaluate Change Controls and CAPA action plans, verifying their effectiveness to ensure resolution of root causes and prevention of recurrence.
- Review all analytical data generated in the Quality Control laboratory, ensuring accuracy and compliance with relevant SOPs.
- Review instrument and equipment calibration records and audit trails to confirm reliability, data integrity, and GMP adherence.
- Prepare and review documentation related to stability samples and ensure that reference standards, impurity standards, working standards, and related records are maintained per applicable procedures.
- Perform and verify SAP transactions related to laboratory workflows and data entries as outlined in SOPs, ensuring traceability and accuracy.
- Review and approve method validation and method transfer protocols and reports, ensuring analytical consistency across platforms.
Eligibility Criteria
- Educational qualification: Graduation in Chemistry/Analytical Chemistry or Pharmacy is mandatory; a Master’s in Microbiology, Biochemistry, Biotechnology, Chemistry/Analytical Chemistry, or Pharmacy is preferred.
- Additional Certifications like CQA, CPGP, CBSP, Six Sigma, ICH Q5/Q6, Advanced Biologics Manufacturing, or RAC are preferred.
- Minimum work experience: 2+ years.
Required Skills
- Regulatory Compliance
- Regulatory Filings
- Technical Documentation
- Change Control
- Laboratory Information
- Risk Management
- Chromatography
- Product Quality (QA/QC)
Additional Information
Benefits Offered: At Dr. Reddy’s, employees benefit from personalized learning programs and industry-standard benefits, including joining & relocation support, family support (Maternity & Paternity benefits), medical coverage, and life coverage.
Our Work Culture: Dr. Reddy’s fosters a culture of empathy and dynamism, believing that people are at the core of their journey. The company supports individual ability while fostering teamwork and shared success.
How to Apply
Interested candidates can apply for the position through the following link: Team Member – Analytical QA.
Conclusion
This Dr Reddy Baddi vacancy for a Team Member in Analytical QA is a significant step for qualified candidates aiming to make a difference in the pharmaceutical industry. Interested individuals are encouraged to apply before the deadline.
