Dr.Reddy's Lab Hiring QA QMS Team Member

Dr.Reddy's Laboratories offers a competitive total rewards package including base salary determined on the basis of role, experience, skill set and location. Additionally, employees are eligible for an annual discretionary bonus, and benefits including comprehensive health care coverage, retirement savings plan and leave benefits. Additional details about total compensation and benefits will be provided during the hiring process.

Post : Team Member - QA QMS

Job Description
1. Handling of QMS activities like change control, Deviations, CAPA, Market complaints Recalls and Returned goods as per the predefined procedure product as per procedure.
2. To involve in Regulatory filings and query response.
3. To access Cross site applicable CAPA at site.
4. To ensure compliance of SOP for closure of Deviations within timelines.
5. To carryout Deviation/Market Complaint/CAPA trends as per procedure.
6. To involve in the Management of Risk Assessments and Risk Summary.
7. Review of all logbooks used in Production, Packing, Quality Control, Engineering & Warehouse area.
8. Ensure the compliance in the manufacturing facility or area with respect to the cleanliness, and labelling as per the cGMP.
9. Responsible to carry out the investigations and timely closure of the same within the time line.
10. To involve in QRM and Tracking actions periodically.

11. To Carry out any other job assigned by the Head of the Department, Quality Assurance.
12. To carry out the Document life cycle management as per the approved procedure and applicable software’s.
13. Annual Product quality review.
14. To participate in handling of internal and external audits (Customers/Regulatory agencies). Coordinate with plant QA for preparation of response and appropriate CAPA.
15. Responsible to evaluate the gaps, with respective to current regulatory expectation and observations in pharmaceutical industry.
16. Initiation and handling of Quality Notification of Deviations, CAPA, OOS & OOT/FAR/QDN/Recall and Change controls through applicable software’s.
17. Review of change controls through as per applicable software.
18. Responsible for participation in the investigations i.e. OOS, OOT, Deviations and ensure its closures within the timelines.
19. Periodic review of the area, equipment and the instruments are in validated and calibrated state.
20. Review of SOP’s, Protocols, Reports, Qualification documents, Deviations/OOS/OOT/Market Complaints/Recalls/FAR/QDN.
21. Responsible for co-ordination with RA for Data Submission.
22. Responsible for maintaining the licenses and Quality Technical Agreements and communication to SCM and RA personnel for license updation

Candidate Profile
Graduation in Pharmacy
Minimum Work Experience
8+ years of experience.
Skills & Attributes Functional Skills
Change Control Coordinator
Market complaint investigator
APQR
Resident Skills
• Current Good Manufacturing Practices (cGMPs)
• 21 CFR Part 210 and 211
Behavioural Skills
• Technical leadership – guides teams in solving complex challenges and driving automation excellence.
• Continuous improvement mindset – fosters a culture of proactive problem-solving, learning, and cost-effective innovation.
Critical Exposures
• 8+ years in roles across QMS systems and Market Complaint investigations

Additional Information
Experience : 8+ years
Qualification : Graduation in Pharmacy
Location : Pydibimavaram, Andhra Pradesh 532409, India
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : QA
End Date : 20th November 2026