Are you a skilled professional in biologics manufacturing, quality assurance in biologics, or upstream downstream processing? Dr. Reddy’s Laboratories, a global leader in biosimilars and innovative biologics, is conducting a lateral hiring drive on 9th November 2025 in Ahmedabad and Pune. With openings in Quality, Manufacturing, MSAT, Engineering, and R&D, this is your chance to join a team driving cutting-edge healthcare solutions.
Dr. Reddy’s Biologics unit in Bachupally/Shamirpet, Hyderabad offers rewarding biologics careers in India with exposure to advanced technologies like mammalian cell culture, chromatography, and automation platforms (ABB800xA, Siemens, Allen Bradley). If you have 3-10 years experience in pharma biologics and expertise in cGMP compliance, don’t miss this opportunity!
Interview Details
Ahmedabad
- Date: 9th November 2025
- Venue: THE FERN RESIDENCY, Near Subhash Bridge Corner, RTO Circle, Ahmedabad, Gujarat 380027
Pune
- Date: 9th November 2025
- Venue: Pune (Exact location shared post-registration)
Apply Now: Scan QR code from official flyer or click https://lnkd.in/g94RYk4R
Key Responsibilities by Role
Team Member – Packing (Visual Inspection & Medical Device Packaging)
- Perform visual inspection and packaging operations per cGMP standards
- Strategic planning, documentation, and compliance in biologics packing
TM Engineering – Drug Substance Mechanical (I&A)
- Handle automation platforms: ABB800xA, Siemens, Allen Bradley PLCs, SCADA
- Maintain bioreactors, TFF, ATF systems under cGMP & QMS
TM Engineering – Drug Product/Sterile/Injectable (I&A)
- Manage vial filling, washing, tunnel automation systems
Team Member – Drug Substance (Upstream/Downstream)
- Execute upstream/downstream unit operations with GMP documentation
Team Member MSAT – Upstream/Downstream
- Expertise in perfusion technology, scale-up, single-use systems, bioreactor characterization, chromatography, ultrafiltration, virus filtration
Development Quality Assurance (Drug Substance/Product/Analytical)
- Ensure quality oversight in development phases
Drug Substance – Quality Assurance (In-Process)
- Upstream/downstream manufacturing quality checks
ASAT-Biosimilar
- Analytical method validation, transfers, real-time investigations
Quality Control – Lab Support
- Equipment qualification, calibration, GxP periodic reviews (GAMPS, 21CFR)
Quality Control – Bioassay
- Cell-based bioassays, SPR, FACS techniques
Quality Control – RM/PM & Analytical
- Material analytics using RP-HPLC, Glycan, SEC, IEX, pep map
Quality Control – Stability
- Stability protocol/report preparation, chamber maintenance per cGMP
Qualifications & Experience Required
- Experience: 3 – 10 years in biologics quality control, manufacturing science, or pharma engineering
- B.Pharm/M.Pharm/B.Tech/M.Tech in Biotechnology, Biochemistry, Chemical Engineering, or related
- Strong knowledge of cGMP in biologics, upstream downstream processing, automation, analytical techniques (HPLC, bioassays)
- Familiarity with regulatory standards (21CFR, GAMPS) essential
Benefits at Dr. Reddy’s Biologics
- Competitive salary & performance incentives
- Global exposure in biosimilars R&D
- Learning opportunities in cutting-edge technologies
- Inclusive culture promoting diversity & work-life balance
- Relocation support for Hyderabad roles
How to Apply
- Carry updated resume, recent payslips, and ID proof
- Walk-in directly on 9th Nov 2025
- Pre-register via application link for faster processing
- Email: Share profile to careers@drreddys.com (mention “Biologics Walk-In 2025”)
FAQs
1. What is the job location for Dr. Reddy’s Biologics roles?
All positions are based in Bachupally/Shamirpet, Hyderabad. Relocation assistance provided.
2. Is prior experience in biosimilars mandatory?
Preferred but not mandatory. Strong cGMP biologics experience in upstream/downstream or quality assurance is sufficient.
