Dr. Reddy’s Laboratories Hiring Team Member – AQA (Quality Assurance)

Team Member – AQA (Quality Assurance) Jobs for Pharmacy, Chemistry, and Chemical Engineering Graduates in Hyderabad. Apply for Team Member – AQA jobs at Dr. Reddy’s Laboratories, Hyderabad. Open to B Pharm, M.Pharm, Chemistry, and Chemical Engineering graduates with 3–7 years’ experience.

Team Member – AQA Jobs in Hyderabad: Quality Assurance Careers at Dr. Reddy’s Laboratories

Are you a skilled quality assurance professional with a background in Pharmacy, Chemistry, or Chemical Engineering? Dr. Reddy’s Laboratories, a global leader in pharmaceutical innovation and manufacturing, is looking for talented candidates to join its Global Manufacturing Organisation (GMO) as a Team Member – AQA in Hyderabad, Telangana. This is your opportunity to advance your career at a company renowned for its commitment to affordable, high-quality medicines and a future-ready, inclusive work culture.

Why Dr. Reddy’s Laboratories?

With a legacy spanning four decades, Dr. Reddy’s Laboratories is driven by the mission “Good Health Can’t Wait.” The company employs over 24,000 professionals worldwide and operates 19 state-of-the-art manufacturing plants across multiple continents. Dr. Reddy’s is recognized for its focus on access, affordability, and innovation in healthcare, as well as its dedication to sustainability, diversity, and employee well-being.

About the Team Member – AQA Role

Location: Hyderabad, Telangana, India
Department: Quality Assurance (GMO)
Experience Required: 3–7 years in pharmaceutical manufacturing or a similar role
Job Type: Full-time

As a Team Member – AQA, you will play a vital role in ensuring the highest standards of analytical quality assurance across Dr. Reddy’s manufacturing operations. This position is ideal for professionals eager to contribute to global healthcare through precision, compliance, and innovation.

Key Responsibilities

• Review and approve all analytical test data from the Quality Control lab.

• Approve and make usage decisions for analytical reports in LIMS, Empower, and SAP systems.

• Provide Level-2 electronic signatures for chromatography data and standalone instruments.

• Review analytical test reports, method validation, and method transfer documents.

• Oversee instrument calibrations and working standard qualification records.

• Manage incidents, deviations, out-of-trend/specification results, and follow up on corrective and preventive actions.

• Monitor analytical activities and ensure cGMP/cGLP compliance.

• Verify specifications, standard test procedures, worksheets, and analytical reports before approval.

• Review audit trails for all relevant systems and ensure data integrity.

• Approve Excel sheet validations and review acceptance of results for APIs, excipients, and packing materials.

• Compile and verify stability data and exhibit batch sampling protocols.

• Handle Robotic Process Automation for Chromatography Data Review (RPACD).

• Support any additional activities as assigned by senior staff.

Qualifications and Eligibility

Required Education:

• Bachelor’s or Master’s degree in Pharmacy (B Pharm/M.Pharm), Chemistry, Chemical Engineering, or a related field.

Experience Required:

• 3 to 7 years of experience in pharmaceutical manufacturing, quality assurance, or a similar role.

Key Skills:

• Strong knowledge of analytical quality assurance, cGMP, and cGLP standards.

• Proficiency with LIMS, Empower, SAP, and chromatography data systems.

• Excellent documentation, analytical, and problem-solving skills.

• Ability to handle deviations, investigations, and regulatory compliance.

• Strong teamwork, communication, and attention to detail.

Benefits

• Competitive salary and benefits package

• Medical and life insurance coverage for self and family

• Relocation and joining support

• Family support (maternity/paternity benefits)

• Learning and development opportunities

• Dynamic, future-ready work culture

How to Apply

Ready to take your quality assurance career to the next level?
Apply now for the Team Member – AQA position at Dr. Reddy’s Laboratories, Hyderabad, and join a company that values expertise, innovation, and integrity.
[Apply here]

Frequently Asked Questions

What is the minimum qualification for this role?
A Bachelor’s or Master’s degree in Pharmacy, Chemistry, Chemical Engineering, or a related field.

Is prior experience mandatory?
Yes, 3–7 years of relevant experience in pharmaceutical manufacturing or quality assurance is required.

Where is the job located?
The role is based in Hyderabad, Telangana, India.

What are the main responsibilities?
Key duties include analytical data review, compliance monitoring, deviation handling, and supporting continuous quality improvement.

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