Join for QA Analyst Job | Explore in Dr. Reddy’s Laboratories careers and Global Manufacturing
Dr. Reddy’s Laboratories is seeking a skilled for a QA Analyst Job Role to join its Global Manufacturing Organisation. This QA Analyst Job Role role Global Manufacturing involves reviewing analytical test data, ensuring cGMP compliance, and managing deviations, method validations, and stability data across APIs, excipients, and packaging materials. Join a leading pharmaceutical company committed to quality, innovation, and global healthcare impact.
About the QA Analyst Job Role
Dr. Reddy’s Laboratories Ltd. is a global pharmaceutical company with over 24,000 employees dedicated to accelerating access to affordable, innovative medicines because Good Health Can’t Wait. Founded in 1984, the company operates in 66 countries with research, manufacturing, and commercial facilities.
With a focus on access, affordability, and innovation, Dr. Reddy’s combines deep science, progressive people practices, and robust governance. Our strategy, “The Next and the New,” emphasizes sustainable growth and reaching over 1.5 billion patients globally by 2030. We maintain an inclusive, equal opportunity work environment, valuing merit, diversity, and talent.
Job Description for QA Analyst Job Role:
Job Summary / Roles & Responsibilities
-
Review and approve analytical test data in QC.
-
Evaluate analytical reports using LIMS, Empower, and SAP.
-
Apply electronic signatures for chromatography data stations (CDS) and standalone instruments.
-
Global Manufacturing deviations.
-
Review reported results against specifications and trends.
-
Review method validation and method transfer documents.
-
Verify instrument calibrations and working standard qualification records.
-
Handle incidents, deviations, OOT/OOS investigations, and CAPA follow-ups.
-
Monitor QC laboratory analytical activities.
-
Verify specifications, test procedures, worksheets, and audit trails.
-
Ensure cGMP/cGLP compliance and adherence to safety, health, and environmental procedures.
-
Approve Excel validations and review results for APIs, excipients, and packaging materials.
-
Compile and verify stability data, exhibit batch sampling protocols, and RPACD activities.
-
Perform other activities assigned by reporting managers.
Qualifications for QA Analyst Job Role:
-
Bachelor’s or Master’s degree in Pharmacy, Chemistry, Chemical Engineering, or related field.
-
3–7 years of experience in QC or AQA departments.
About the Department – Global Manufacturing Organisation (GMO)
Global Manufacturing involved in Dr. Reddy’s GMO drives global healthcare impact through precision manufacturing and innovation. Operating 19 state-of-the-art plants across India, Mexico, and Europe, GMO includes 8 OSD facilities, 3 Injectables facilities, and 8 API facilities.
We produce complex APIs and maintain over 1,150 drug master files across therapy areas such as Oncology, Cardio-vascular, CNS, and Anti-Diabetes. Recognized by the World Economic Forum as a Global Lighthouse Network site, our facilities emphasize operational excellence, productivity improvement, and digitalization, creating “factories of the future.”
Benefits Offered for QA Analyst Job Role:
-
Personalized learning and professional development programs offered by Dr. Reddy’s Laboratories careers knowledge about Global Manufacturing .
-
Competitive benefits including relocation support, family assistance, maternity/paternity benefits, medical coverage, and life insurance.
Our Work Culture
Dr. Reddy’s credo, “Good Health Can’t Wait,” guides our culture of empathy, innovation, and collaboration. Employees thrive in an enabling environment that supports teamwork, diverse skillsets, and shared success.
