QA Associate – CAR-T at Dr. Reddy’s l Bachelor’s in Pharma Candidates Apply Now
Are you passionate about quality and innovation in biologics? Dr. Reddy’s Laboratories is hiring a Quality Assurance Associate (CAR-T) to join its cutting-edge GMP cell therapy facility in Bengaluru. This role offers a unique opportunity to work at the forefront of CAR-T and gene therapy manufacturing, ensuring product quality and regulatory compliance in a purpose-driven, global pharmaceutical environment. Apply now to be part of a company transforming healthcare with science, sustainability, and innovation at its core.
Quality Assurance Associate (CAR-T)
Location: Bengaluru, Karnataka, India
Company: Dr. Reddy’s Laboratories Ltd.
Type: Full-Time | On-Premise
Job Family: Quality | Sub-Family: Quality Assurance
Experience: 2–6 Years
Business Unit: Biologics
Company Overview
Dr. Reddy’s Laboratories Ltd. is a global pharmaceutical leader dedicated to affordable and innovative medicines. With a presence in 66 countries and over 24,000 employees, we strive to accelerate access to good health. Our purpose: Good Health Can’t Wait.
Position Summary
We seek a collaborative, quality-focused professional to support QA operations at our new CAR-T cell therapy GMP facility in Bengaluru. The role involves working closely with cross-functional teams and implementing a robust quality management system in compliance with global regulatory standards.
Responsibilities
- Assist in establishing and maintaining a quality management system per cGMP guidelines.
- Provide QA oversight for all GMP-related operations and quality control.
- Review and maintain documentation: change controls, deviations, complaints, investigations.
- Collaborate across departments to ensure compliance with company and regulatory standards.
- Support QA activities during commissioning and qualification phases.
- Draft and review SOPs, regulatory documents, and controlled documentation.
- Participate in audits and inspections when required.
- Perform tasks necessary to maintain cGMP compliance and product quality.
Behavioral Skills Required
- Communication: Clear and effective with internal teams.
- Critical Thinking: Ability to evaluate data and take informed actions.
- Problem-Solving: Analytical mindset for compliance and operational issues.
- Teamwork: Cooperative across functional teams.
- Time Management: Prioritize work and meet deadlines efficiently.
Qualifications
- Bachelor’s or higher degree in Pharmacy or a related Life Sciences field.
- 2–6 years of biopharmaceutical or cell therapy QA experience.
- Preferably experienced in Cell and Gene Therapy products.
- Strong understanding of Good Manufacturing Practices (GMP).
- Familiarity with FDA, EU, and local compliance requirements.
Why Join Dr. Reddy’s?
At Dr. Reddy’s, you’ll be part of a globally respected organization that’s future-ready and committed to sustainability, innovation, and healthcare accessibility. Join us to work on next-gen cell therapies in a diverse and inclusive workplace that values your skills and ideas.
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