Dr. Reddy’s Laboratories: Team Member - QA QMS — Pydibimavaram, AP, India
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Dr. Reddy’s Laboratories lists a Team Member - QA QMS opening in Pydibimavaram, AP, India. The position is listed as full-time. The job description covers quality control, quality assurance, manufacturing, pharmacy, audit, compliance, warehouse operations.
Recruitment overview
| Organisation | Dr. Reddy’s Laboratories |
|---|---|
| Post / role | Team Member - QA QMS |
| Employment type | Full-time |
| Notification / job ID | REF26392K |
| Job location | Pydibimavaram, AP, India |
| Work arrangement | On-site |
| Educational qualification | See the employer’s role-specific qualification criteria |
| Experience required | 8+ years of experience |
| Salary / stipend | See employer notice for pay details |
| Last date to apply | See official notice |
About Dr. Reddy’s Laboratories
Dr. Reddy’s Laboratories is a pharmaceutical business with research and development, medicine-manufacturing and commercial activities. Its employer description centres on making affordable and innovative medicines accessible. The organisation connects scientific development with the production and delivery of pharmaceutical products, rather than operating only as a research laboratory. Its published business priorities include strengthening existing medicine activities, developing future opportunities and conducting operations with attention to people, resources and corporate governance.
The position and its setting
Dr. Reddy’s Laboratories lists Team Member - QA QMS in Pydibimavaram, AP, India, under reference REF26392K. The details below separate the work described by the employer from essential conditions, preferred experience and practical preparation advice.
- Employment type: Full-time
- Employer listing date: 21 October 2026
- Job Family: Quality
- Brands: Dr Reddy's Laboratories Limited
Responsibilities and work described
- Roles & Responsibilities:
- Handling of QMS activities like change control, Deviations, CAPA, Market complaints Recalls and Returned goods as per the predefined procedure product as per procedure
- To involve in Regulatory filings and query response
- To access Cross site applicable CAPA at site
- To ensure compliance of SOP for closure of Deviations within timelines
- To carryout Deviation/Market Complaint/CAPA trends as per procedure
- To involve in the Management of Risk Assessments and Risk Summary
- Review: of all logbooks used in Production, Packing, Quality Control, Engineering & Warehouse area
- Quality / delivery: the compliance in the manufacturing facility or area with respect to the cleanliness, and labelling as per the cGMP
- Responsible to carry out the investigations and timely closure of the same within the time line
- To involve in QRM and Tracking actions periodically
- To Carry out any other job assigned by the Head of the Department, Quality Assurance
- To carry out the Document life cycle management as per the approved procedure and applicable software’s
- Annual Product quality review
- To participate in handling of internal and external audits (Customers/Regulatory agencies)
- Coordination: with plant QA for preparation of response and appropriate CAPA
Essential requirements and candidate background
- Educational Qualification
- 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
Location, schedule and contract conditions
- Work arrangement: On-site
- Advertised location: Pydibimavaram, AP, India
Pay and application dates
A verified salary figure is not established in this article. An online estimate for another Team Member - QA QMS vacancy is not an offer for reference REF26392K; use the employer’s own pay disclosure and recruitment communication.
A closing date is not confirmed in this article. Check the current employer page before submitting: an undated posting can change or be withdrawn.
How to apply to Dr. Reddy’s Laboratories
Applications follow the official employer page linked below.
Open the official Dr. Reddy’s Laboratories posting below and match the title and reference REF26392K.
Compare your qualifications and experience with the essential conditions for the Pydibimavaram, AP, India position, then read the preferred criteria separately.
Prepare an accurate CV and the supporting items requested in that employer’s application. Provide only information and documents you are authorised to share.
Use the employer’s application option, complete the required fields and review the submission. Retain the acknowledgement when one is provided. Job Alerts World does not receive the application.
Practical preparation: GMP
GMP references concern work performed within a controlled manufacturing or quality environment. In an application, explain your actual involvement with procedures, records, deviations or other controls relevant to the post.
Relevant skills
- GMP
- quality control
- quality assurance
- manufacturing
- pharmacy
- audit
- compliance
- warehouse operations
- communication
Important links
| Official notification / job description | Open official page |
|---|
Read the complete official notice before applying. Availability and requirements can change.
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