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Dr Reddy’s Laboratories, one of India’s most respected global pharmaceutical companies, is inviting applications for the position of Team Member – Analytical Quality Assurance (AQA) at its Hyderabad facility. This opportunity is ideal for experienced pharmaceutical professionals who have a strong background in Quality Control (QC) or Analytical Quality Assurance and are looking to advance their careers in a world-class pharma organisation.
For professionals aiming to work in a regulated environment with global exposure, advanced analytical systems, and strict compliance standards, this role offers excellent long-term career stability and growth.
Dr Reddy’s Laboratories is a globally recognised pharmaceutical company committed to providing affordable, innovative, and high-quality medicines to patients across the world. The company was founded in 1984 and is headquartered in Hyderabad, Telangana, India.
With a strong global footprint across multiple countries and regulated markets, Dr Reddy’s has built a solid reputation in research & development, quality systems, regulatory compliance, and sustainable healthcare solutions. The organisation employs over 24,000 professionals worldwide, working across manufacturing, R&D, quality, regulatory affairs, and commercial operations.
Dr Reddy’s Laboratories follows high ethical standards, scientific excellence, and continuous improvement practices in all its pharmaceutical activities. Working at Dr Reddy’s means being part of a professionally driven, innovation-focused culture that values learning, compliance, and quality-driven processes while contributing to global healthcare improvement.
The Team Member – Analytical QA role is a critical position within the quality framework of Dr Reddy’s Laboratories. The selected candidate will ensure the accuracy, integrity, and compliance of analytical data generated by the Quality Control department.
This role involves reviewing analytical reports, managing deviations, handling electronic systems, and ensuring compliance with cGMP and cGLP guidelines. Professionals working in this position directly contribute to maintaining global quality standards and regulatory readiness.
Job Title: Team Member – Analytical Quality Assurance (AQA)
Department: Analytical QA / Quality Control
Employment Type: Full-Time
Work Location: Hyderabad, Telangana
Industry: Pharmaceutical Manufacturing
Selected candidates will be responsible for a wide range of analytical quality assurance activities, including:
Reviewing and approving analytical test data generated by the Quality Control department
Handling electronic systems such as LIMS, Empower, and SAP for data analysis and reporting
Providing Level-2 electronic signatures for Chromatography Data Station (CDS)
Reviewing validation, method transfer, and analytical test reports
Monitoring instrument calibration and qualification records
Managing deviations, incidents, OOS/OOT investigations, and ensuring CAPA implementation
Ensuring strict compliance with cGMP / cGLP guidelines
Verifying specifications, analytical procedures, worksheets, and reports
Reviewing compiled stability data and supporting batch sampling activities
Supporting Robotic Process Automation (RPA) initiatives in chromatography data review
This role requires strong analytical understanding, documentation skills, and attention to regulatory compliance.
Candidates applying for this position must meet the following eligibility requirements:
Educational Qualification: Bachelor’s or Master’s degree in Pharmacy, Chemistry, Chemical Engineering, or a related discipline
Experience: Minimum 3–7 years of relevant experience in Quality Control or Analytical Quality Assurance within the pharmaceutical industry
To succeed in this Analytical QA role, candidates should possess:
Strong understanding of analytical quality assurance processes
Practical knowledge of cGMP, cGLP, and data integrity requirements
Hands-on experience with LIMS, Empower, CDS, and SAP systems
Ability to handle OOS, OOT, deviations, and CAPA investigations
Good documentation, data review, and compliance skills
Analytical mindset with attention to detail
Ability to work independently and in cross-functional teams
The estimated salary for this position ranges between ₹6,00,000 to ₹12,00,000 per annum, depending on the candidate’s experience, skill set, and interview performance. Dr Reddy’s Laboratories also offers additional benefits such as medical insurance, learning programs, and career development support.
Interview Mode: Company selection process (screening + interview)
Work Location: Hyderabad, Telangana
Shortlisted candidates will be contacted by the recruitment team for further interview rounds.
Candidates should keep the following documents ready during the selection process:
Updated resume/CV
Educational certificates and mark sheets
Experience letters from previous employers
Last drawn salary slips (if applicable)
Valid photo identity proof
Q1. Is this job suitable for freshers?
No. This role requires 3–7 years of prior experience in QC or Analytical QA.
Q2. Is experience with LIMS or Empower mandatory?
Yes, hands-on experience with analytical systems like LIMS or Empower is highly preferred.
Q3. What is the work location for this job?
The position is based in Hyderabad, Telangana.
Q4. Does Dr Reddy’s offer long-term career growth?
Yes, Dr Reddy’s Laboratories provides excellent learning opportunities and long-term career development.
If you are an experienced pharmaceutical professional with expertise in Analytical Quality Assurance or Quality Control, this opportunity at Dr Reddy’s Laboratories can significantly boost your career. With strong exposure to global quality systems, advanced analytical tools, and a professional work culture, this role offers both stability and growth.
Apply early to secure your chance to work with one of India’s most trusted pharmaceutical organisations.
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