Dr. Reddy’s maintains a work environment, free from discrimination, and is an equal opportunity employer. The company is committed to equal employment opportuninty and employs all qualified persons without regard to race, colour, religion, national origin, sex, age, disability status, genetics, sexual orientation, gender identity or expression, marital status, citizenship or any other characteristic or classification protected by the applicable law(s) of the countries we operate in. We apply these principles in all aspects of employment, including recruitment, hiring, placement, promotion, termination, lay off, transfer, leaves of absence, training and compensation. If you feel you have not been treated in accordance with these principles, you should contact your local Human Resources Department. The company assures all employees that no individual filing a complaint will be discriminated against, as a result of their complaint
Dr. Reddy’s Laboratories Ltd. is an Indian multinational pharmaceutical company based in Hyderabad, with U.S. headquarters in East Brunswick, New Jersey. The company was founded by Kallam Anji Reddy, who previously worked in the mentor institute Indian Drugs and Pharmaceuticals Limited.
DATE AND TIME:
- Date: 30th August 2026 (Sunday)
- Time : 9:00 AM – 3:00PM
- Location: Aurigene Oncology Limited,39-40, KIADB Industrial Area, Electronic City Phase II, Hosur Road, Bangalore
At Dr. Reddy’s Biologics, you’ll have the opportunity to:
Work on cutting-edge biologics and biosimilars
Drive innovation that impacts patients globally
Accelerate your professional growth in a purpose-driven organization
Interested candidates can apply through the registration link/QR code provided in the flyer: https://lnkd.in/dci9XRyc
JOB DETAILS:
- Experience Required: 5–9 years
- Qualifications: Bachelor’s or Master’s degree in Biotechnology, Microbiology, or Biochemistry
Open Roles:
- Quality Assurance – Microbiology Reviewer: Expertise in pharmaceutical microbiology (MLT, Water, BET, Bioburden, Environmental Monitoring, Sterility, Media Fill) and aseptic manufacturing compliance.
- Quality Control – Molecular Biology: Execute molecular biology assays (SDS-PAGE, ELISA, HCP, PAL, PCR-based HCD assays, CE-SDS, Mycoplasma, Western blot) for batch release and stability.
- Quality Control – In Process / Lab Support: Analytical testing of biosimilars using chromatographic techniques (RP-HPLC, SEC, IEX, Glycan & Peptide Mapping) and GMP-compliant lab operations.
- Quality Assurance – SIT: Investigation capabilities across QC, Drug Substance, and Drug Product for root cause analysis, CAPAs, and regulatory compliance.
- Drug Substance – Quality Assurance: In-process quality assurance for drug substance manufacturing (upstream and downstream).
- Quality Control – Bioassay: Cell-based bioassays, SPR techniques, and FACS techniques.
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Roles & Experience :
- Team Leader – HVAC & Clean Utilities: 5–12 years
- Team Member – Drug Substance: 2–8 years
- TM Engineering – Drug Product/Drug Substance (I&A): 5–12 years
- TM Engineering – DP/DS Mechanical: 5–12 years
- MSAT Specialist – Drug Product: 5–12 years
- MSAT Specialist – Upstream: 5–12 years
Eligible Qualifications:
- Diploma, B.Tech, M.Tech, B.Sc, M.Sc, or B.Pharma
For More JOB Updates Join Our Whatsapp Group CLICK HIRE
