Dr. Reddy’s Quality Assurance Associate Jobs – Hyderabad & Bachupally

Published on: November 6, 2026

Dr. Reddy’s Laboratories has listed two Quality Assurance Associate job opportunities under its Biologics division. The openings are for Drug Product QA in Hyderabad and Drug Substance QA in Bachupally, Telangana.

The positions require 8–10 years and 6–8 years of experience, respectively. Candidates with relevant pharmaceutical or biopharmaceutical Quality Assurance and Manufacturing experience can review the eligibility criteria and apply through the company’s recruitment portal.

Preparing for a QA role? You can also practice with our Free Pharma Quality Assurance Mock Test – 50 MCQs with Certificate. You can also explore more opportunities on our QA/QC Jobs page.

1. Dr. Reddy’s Quality Assurance Jobs – Overview

2. Available Quality Assurance Positions

The two positions have different educational qualifications and experience requirements. Candidates should check the details carefully before applying.

3. Quality Assurance Associate – Drug Product

Company: Dr. Reddy’s Laboratories

Location: Hyderabad, Telangana

Vacancy ID: 5587

Experience: 8–10 years

Qualification: Bachelor’s or Master’s in Life Sciences

This position focuses on Quality Assurance activities during drug product manufacturing. The selected candidate will work with manufacturing teams to maintain GMP compliance and ensure that production and packaging activities follow approved procedures.

Experience with injectable products is particularly relevant to this role.

3.1. Manufacturing and Shop-Floor Activities

• Monitor manufacturing operations, including formulation, filling, optical inspection and packaging.
• Perform line clearance activities and ensure compliance with approved procedures.
• Monitor shop-floor practices to maintain GMP standards.
• Review aseptic media fill simulation protocols and reports and support execution activities.

3.2. Documentation and Batch Record Review

• Review Master Formula Records (MFRs), Bills of Materials (BOMs) and Batch Production Records (BPRs).
• Verify GMP records in accordance with ALCOA data integrity principles.
• Review manufacturing documents, SOPs and validation protocols.
• Ensure that required documentation is complete and properly maintained.

3.3. Quality Systems and Investigations

• Review change controls, incidents and Corrective and Preventive Actions (CAPAs).
• Participate in investigations related to deviations and market complaints.
• Support Out-of-Specification (OOS) and Out-of-Limit (OOL) investigations.
• Participate in internal and external audits.
• Support the preparation and review of Annual Product Quality Review (APQR) reports.

3.4. Product Quality and Compliance

• Monitor control sample management.
• Check refrigeration time-out requirements and material management.
• Support transport validation activities.
• Verify temperature records for export shipments.
• Review equipment audit trails and related quality records.

3.5. Qualification and Experience

Candidates with experience in injectable manufacturing, aseptic operations, GMP documentation, investigations and quality systems may find this position relevant.

Apply Online: Quality Assurance Associate – Drug Product, Hyderabad

4. Quality Assurance Associate – Drug Substance

Company: Dr. Reddy’s Laboratories

Location: Bachupally, Telangana

Vacancy ID: 5585

Experience: 6–8 years

Qualification: M.Sc. Life Sciences / M.Pharm

The Drug Substance QA position involves quality oversight of biopharmaceutical manufacturing activities, particularly in the biosimilars area.

The role covers cell bank management, manufacturing documentation, GMP compliance, investigations, validation and quality system activities. Candidates should have relevant experience in Quality Assurance and Manufacturing.

4.1. Cell Bank Management

• Oversee qualification, documentation and traceability of Master Cell Banks (MCB) and Working Cell Banks (WCB).
• Review cell bank protocols, Certificates of Analysis (COAs) and characterization reports.
• Monitor storage conditions and alarm systems for liquid nitrogen (LN2) tanks and freezers.
• Coordinate cell bank-related activities with manufacturing, QC and other teams.
• Handle cell bank-related deviations, CAPAs and change controls.
• Manage the issuance of cell banks for manufacturing activities.

4.2. Batch Documentation and Quality Systems

• Review Drug Substance Batch Production Records (BPRs).
• Review and approve MFRs, BPRs, BOMs, SOPs and Product Quality Reviews (PQRs), as applicable to the role.
• Review technology transfer protocols and reports.
• Handle investigations related to discrepancies and quality issues.
• Review CAPAs, change controls and Quality Risk Management (QRM) activities.
• Ensure timely deposition of reviewed documents to DCQA.

4.3. GMP Compliance and Manufacturing Support

• Monitor manufacturing activities to ensure compliance with GMP requirements.
• Conduct routine and non-routine shop-floor inspections.
• Perform line clearance during product changeovers.
• Ensure that manufacturing operations follow approved SOPs.
• Verify GMP records in accordance with ALCOA+ data integrity principles.
• Support internal and external audits.

4.4. Qualification, Validation and Audit Trail Review

• Review process qualification and cleaning validation protocols and reports.
• Review technology transfer documentation.
• Perform system and process audit trail reviews.
• Review equipment audit trails according to the defined schedule.
• Support the closure of audit observations and related corrective actions.

4.5. Qualification and Experience

4.6. Additional Requirements

Candidates should have an understanding of GMP requirements, biopharmaceutical manufacturing and quality systems. The job description also refers to compliance with EU Annex 1 and applicable ICH guidelines.

Good communication, analytical thinking and coordination skills are important for this role.

Shift Requirement: Candidates should be comfortable working in rotational shifts, including nights, weekends and holidays, depending on operational requirements.

Apply Online: Quality Assurance Associate – Drug Substance, Bachupally

5. About Dr. Reddy’s Laboratories

Dr. Reddy’s Laboratories is an Indian multinational pharmaceutical company established in 1984. It develops, manufactures and markets pharmaceutical products for patients in India and international markets.

The company operates across several pharmaceutical business areas, including its Biologics division, which focuses on the development and commercialization of biosimilar products.

These two job listings are within the company’s Quality Assurance function and involve different areas of biopharmaceutical manufacturing.

6. How to Apply for Dr. Reddy’s QA Associate Jobs

Candidates who meet the eligibility requirements can apply online through the official Dr. Reddy’s Laboratories careers portal.

6.1. Steps to Apply Online

1. Open the application link for your preferred position.
2. Read the complete job description and check the required qualifications and experience.
3. Select the Apply option and follow the instructions displayed on the recruitment portal.
4. Enter the requested personal, educational and employment details.
5. Upload your updated resume and any other documents requested.
6. Review the information carefully before submitting the application.
7. Submit the application and save the confirmation for future reference.

6.2. Direct Application Links

Before applying: Check whether the respective vacancy is still accepting applications on the official careers portal. Make sure your resume clearly mentions your relevant manufacturing, Quality Assurance and documentation experience.

7. Frequently Asked Questions

7.1. How many Quality Assurance positions are listed at Dr. Reddy’s Laboratories?

Two Quality Assurance Associate job listings are covered in this article: Drug Product and Drug Substance, both under the Biologics division.

7.2. Where are these positions located?

The Drug Product position is based in Hyderabad, while the Drug Substance position is based in Bachupally, Telangana.

7.3. What is the experience requirement for the Drug Product QA position?

The Drug Product position requires 8–10 years of pharmaceutical industry experience, particularly with injectable products.

7.4. What is the experience requirement for the Drug Substance QA position?

Candidates need 6–8 years of industrial experience in Quality Assurance and Manufacturing, with relevant biosimilars experience.

7.5. What qualifications are required for these positions?

For Drug Product QA, a Bachelor’s or Master’s degree in Life Sciences is required. For Drug Substance QA, the specified qualifications are M.Sc. Life Sciences or M.Pharm.

7.6. Are these positions suitable for freshers?

No. Both positions require several years of relevant industry experience.

7.7. Is shift work required for the Drug Substance position?

Yes. The job description mentions flexibility to work in rotational shifts, including nights, weekends and holidays.

7.8. How can candidates apply for these vacancies?

Candidates can use the individual application links provided in the job details. Applications are submitted through the official Dr. Reddy’s careers portal.

8. Explore More Pharma Jobs and Career Resources

Disclaimer: PharmaCareerUpdates.com is an independent pharmaceutical career information platform and is not affiliated with Dr. Reddy’s Laboratories. Job information is based on the supplied recruitment listings. Vacancy status and application requirements may change. Candidates should verify the latest details on the official company careers portal before applying.