Dr.Reddy’s Biologics is an Indian multinational pharmaceutical company As an integrated global pharmaceutical company, we operate through three core segments – Pharmaceutical Services and Active Ingredients, Global Generics and Proprietary Products. Dr. Reddy’s Laboratories located in AP & Telangana.
DATE AND TIME:
- Date: Sunday, 14th Sept 2025
- Time: 9:00 AM – 3:00 PM
- Venue: Aurigene Oncology Ltd., 39-40, KIADB Industrial Area, Electronic City Phase II, Hosur Road, Bangalore – 560100
Apply Now: Click on the link : Click Here or Scan below QR Code in the flyer
Job Details:
- Qualification: B.Tech / Masters in Biotechnology / Microbiology / Biochemistry
- Experience: 3–10 Years
POSITIONS:
Open Roles – Team Member / Team Leader:
- Development Quality Assurance – Drug Substance, Drug Product, Analytical
- Drug Substance QA – In-Process QA (Upstream/Downstream Manufacturing)
- Quality Control – Bioassay – Cell-based assays, SPR, FACS
- QC – Molecular Biology – ELISA (HCP, PAL), RT-PCR, SDS-PAGE
- ASAT – Biosimilars – Method Transfers, Validations, Regulatory Queries
- Drug Substance Operations – Upstream & Downstream with GMP compliance
Job Details:
- Qualification: Diploma/B.Tech, B.Sc, M.Sc, B. Pharm
- Experience: 3-10 Years
- Apply Now: Click on the link : Click Here or Scan below QR Code in the flyer
Openings for Team Member (TM) & Team Lead (TL) positions:
01. TM-Drug Product/Sterile/Injectable Mechanical
- Vial Filling, Washing, Tunnel, VHP,PFS, Autoclave, Isolator, QMS, PLC SCADA, HMI (Understanding the program & Trouble shooting).
02. TM/TL-Drug Product/Sterile/Injectable (I&A)
- Instrumentation & Automation Vial Filling, Washing, Tunnel, VHP,PFS, Autoclave, Isolator, QMS, PLC, SCADA, HMI
03. TM/TL-Drug Substance (I&A)
- Instrumentation & Automation: Automation Platforms: ABB800xA, Siemens/Allen-Bradley PLCs, SCADA systems, Biopharma Equipment’s (bioreactors, TFF, ATF), cGMP & QMS
04. TM/TL-Drug Substance Mechanical
- I&A: Automation Platforms: ABB800xA, Siemens/Allen-Bradley PLCS, SCADA systems, Biopharma Equipment’s (bioreactors, TFF, ATF), cGMP & QMS
05. Drug Product-Sterile Operations/Fill finish / QMS
- Experience in DP-filling/washing and sterilization operations within GMP (Good Manufacturing Practices), MES, QMS.
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