Unlock rewarding QA jobs in pharmaceuticals! Dr. Reddy’s Laboratories seeks experienced Quality Assurance professionals for full-time roles in Pydibimavaram, Andhra Pradesh. Advance your career in India’s leading pharma innovation hub.
Contents
About the Company
Dr. Reddy’s Laboratories Ltd. is a global pharmaceutical powerhouse headquartered in Hyderabad, India, with operations spanning 66 countries. Founded in 1984, the company employs over 24,000 people dedicated to affordable, innovative medicines under the motto “Good Health Can’t Wait.”
It boasts 19 state-of-the-art manufacturing plants, including API facilities in Srikakulam district, Andhra Pradesh, emphasizing sustainability, R&D excellence, and regulatory compliance like USFDA approvals. Dr. Reddy’s fosters diversity, equal opportunity, and a culture of empathy and dynamism.
Job Details
- Company Name: Dr. Reddy’s Laboratories Ltd.
- Experience: 6–12 years
- Qualification: Bachelor’s degree in Pharmacy, Chemistry, Chemical Engineering, or related field
- Location: Pydibimavaram, Andhra Pradesh, India
- Work Type: Full-time, On-Premise
Job Description
Dr. Reddy’s Laboratories is hiring for the Quality Assurance team within the Global Manufacturing Organisation (GMO). This role focuses on ensuring compliance in manufacturing processes at the Pydibimavaram facility.
Team Member – QA
- Department: Quality Assurance (QA)
- Role: Ensure line clearance, material verification, in-process checks, and batch record compliance
- Experience: 6–12 years
- Education/Qualification: Bachelor’s in Pharmacy, Chemistry, Chemical Engineering, or related
Skills/Qualifications
- Bachelor’s degree in Pharmacy, Chemistry, Chemical Engineering, or equivalent
- 3–7 years minimum in pharmaceutical manufacturing (6–12 preferred for this role)
- Knowledge of aseptic practices, cleaning/process validation, and sampling standards
- Expertise in equipment qualifications (IQ, OQ, PQ), utilities, and area qualifications
- Familiarity with media fill simulations, isolator technology, and lyophilizer operations
- Proficiency in line clearance, material verification, and in-process checks per batch records
- Experience in sampling/testing in-process, reserve, finished, stability samples, and environmental monitoring
- Skilled in reviewing and certifying batch manufacturing/packing records
- Ability to work in IPQA and qualification activities
Key Responsibilities
- Perform line clearance, material verification, start-up, and in-process checks per batch records
- Conduct timely sampling and testing of in-process, reserve, finished, stability samples, and environmental monitoring
- Coordinate cleaning validation activities, including sampling and compliance
- Implement and comply with technology transfer and exhibit batch initiation
- Review and certify batch manufacturing and packing records post-execution
Benefits/Perks
- Personalized learning programs for career growth and development
- Competitive industry-standard benefits including medical and life coverage for family
- Joining and relocation support, maternity/paternity benefits
- Opportunities in innovative manufacturing with digitalization focus
- Collaborative culture emphasizing empathy, teamwork, and sustainability
- Contribution to global healthcare reaching 1.5 billion patients by 2030
How to Apply
Visit the Dr. Reddy’s career portal at careers.drreddys.com to apply online. Submit your resume and cover letter highlighting relevant QA experience. For more details, explore the full job listing.
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Why You Should Join
Dr. Reddy’s offers a transformative platform in pharmaceutical QA at its cutting-edge Pydibimavaram plant, part of a network recognized for excellence. Thrive in a purpose-driven environment focused on innovation, sustainability, and patient impact, with robust growth opportunities and a diverse, inclusive culture.
Build your legacy in global healthcare while enjoying top-tier benefits and professional development. Discover more pharma job opportunities.
FAQs
Q1: What experience is required for the QA Team Member role at Dr. Reddy’s?
A: 6–12 years in pharmaceutical manufacturing, with a minimum of 3–7 years in QA processes.
Q2: Which qualifications are needed for this Quality Assurance position?
A: Bachelor’s degree in Pharmacy, Chemistry, Chemical Engineering, or a related field.
Q3: What are the key technical skills for this QA job?
A: Expertise in validation activities, equipment qualifications, sampling, and batch record reviews; knowledge of isolator and lyophilizer technology.
Q4: How can I apply for the Team Member – QA role?
A: Apply online through careers.drreddys.com with your resume and relevant documents.
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