Analytical QA at Dr Reddy’s Laboratories | Apply Now
An Analytical QA Job opportunity is available at Dr Reddy’s Laboratories in Baddi, Himachal Pradesh, for aspiring Quality Assurance Specialists. This role focuses on ensuring compliance with regulatory standards in Quality Control laboratory operations. Interested candidates are encouraged to apply before the deadline.
- Post: Team Member – Analytical QA
- Location: Baddi, Himachal Pradesh
About Dr Reddy’s Laboratories
Dr Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company operating in the healthcare sector. Established in 1984, the company has grown significantly and now has a presence in 66 countries. With over 24,000 employees, Dr Reddy’s is committed to accelerating access to affordable and innovative medicines, aiming to reach over 1.5 billion patients globally by 2030. The organisation values diversity and is dedicated to maintaining a work environment free from discrimination.
Job Description
In this Analytical QA Job, the Quality Assurance Specialist will participate in investigations of Quality Management System (QMS) documents, prepare trending reports, evaluate Change Controls, review analytical data, and ensure compliance with GMP and GLP standards. 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.
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, and working standards 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. 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 of experience.
Required Skills
- Regulatory Compliance
- Regulatory Filings
- Technical Documentation
- Change Control
- Laboratory Information
- Risk Management
- Chromatography
- Product Quality (QA/QC)
This Analytical QA Job at Dr Reddy’s Laboratories presents a compelling opportunity for qualified candidates to step into a vital role in Quality Assurance. Interested individuals are encouraged to apply at the earliest to join a company committed to innovation and patient care.
