Dr. Reddy’s Biologics Hiring Drive in Ahmedabad!
Exciting news! We’re bringing our lateral hiring drive to Ahmedabad — and we’re looking for talented professionals ready to take the next step in their careers.
Walk-In Interview Details:
- Interview Location: Venue – THE FERN RESIDENCY
Near Subhash Bridge Corner, RTO Circle
Ahmedabad Gujarat 380027
Ahmedabad - Date: 9th November 2025
Job Details:
- Roles: In Quality & Manufacturing
- Experience: 2-8years
- Job Location: Bachupally / Shamirpet Hyderabad
Open Positions:
Team Member – Packing
- Skill in medical device packaging and visual inspection with expertise in strategic planning, documentation, aligned with cGMP standards
TM Engineering – Drug Substance Mechanical
- Instrumentation & Automation: Automation Platforms ABB800xA, Siemens, Allen Bradley PLCS, SCADA system, Biopharma Equipment’s (Bioreactors, TFF, ATF) cGMP & QMS
TM Engineering – Drug Product / Sterile/Injectable (I&A)
- Instrumentation & Automation: Automation Platforms Vial Filing, Washing, Tunnel
Team Member – Drug Substance -Upstream / Downstream
- Execute Downstream/Upstream unit operations, ensuring documentation and compliance within GMP (Good Manufacturing Plant)
Team Member MSAT – Upstream / Downstream
- We are seeking a skilled professional to serve as a specialist in upstream/downstream operations, specializing in processes like mammalian cell culture, perfusion technology, scale-up, single use technology, Bioreactor characterization, Chromatography, Ultrafiltration, and Virus Filtration
Join our What’s Groups for Daily Updates – Click Here
Join Telegram – Click Here
Development Quality Assurance
- Development Quality Assurance in Drug Substance, Drug Product and Analytical
Drug Substance – Quality Assurance
- Quality Assurance-In Process-Drug Substance Manufacturing, Upstream, Downstream
ASAT-Biosimilar
- Analytical method transfers, analytical method validation, real time investigations, annual method performance, addressing regular queries.
Quality control- Lab support
- To plan and execute the equipment’s qualification and calibration activities.
- Execution of routine periodic review of GxP. As per GAMPS and 21CFR compliance.
Quality Control – Bioassay
- Experience in cell-based bioassays, SPR Techniques, FACS techniques.
Quality Control-RM/PM
- Experience in Material analytics lab, strong understanding and adherence to GLP and knowledge of safety practices. Experience in analysis of samples using analytical techniques.
Quality Control Associate Analytical
- Perform analysis in laboratory for the biosimilar /biologics Products, perform chromatography techniques like RP- HPLC, Glycan, SEC, IEX, pep map
Quality control-Stability - Preparation of stability study protocols and reports for drug substance and drug product stability studies. Planning of stability batches issuance. Maintenance of stability chambers as per cGMP compliance.
If you’re passionate about innovation, collaboration, and making an impact — we want to meet you! Come join a team that values growth, diversity, and excellence.
Interested candidates can apply via [Insert application link or email]. Tag someone who should be there!
Join our What’s Groups for Daily Updates – Click Here
Join Telegram – Click Here