Dr. Reddy’s Laboratories – Career Expo in Pune for R&D Roles
Dr. Reddy’s is hosting a Career Expo in Pune to hire experienced professionals for its Biologics R&D division. Join a team committed to innovation and excellence in healthcare.
Walk-In Interview Details
Date: Sunday, 09th November 2025
Time: 9:00 AM onwards
Venue: Sayaji Hotel, 135/136, Mumbai-Bangalore Bypass Highway, Shankar Kalat Nagar, Wakad, Pune, Pimpri-Chinchwad, Maharashtra
Work Location: Bachupally / Shamirpet, Hyderabad
Open Positions and Eligibility Criteria
A.Hiring for Team Member / Team Lead R&D Roles
Experience Required: 3 to 10 years
Qualifications: B.Tech or Master’s in Biotechnology / Microbiology / Biochemistry
1.Research Associate / Team Lead – Upstream / Downstream
Expertise in mammalian cell culture and process development
2.Research Associate / Team Lead – Biological Sciences
Experience in biological product development, characterization, and method development
3.Research Associate / Team Lead – Analytical Development
Proficiency in analytical techniques for biomolecule characterization and method development
4.Research Associate / Team Lead – Formulation & DP
Experience in biologics formulation, drug product process, and device development
B.Hiring for Team Member Quality Roles
Experience Required: 3 to 10 years
Qualifications: B.Tech or Master’s in Biotechnology / Microbiology / Biochemistry
1.Development Quality Assurance
Development Quality Assurance in Drug Substance, Drug Product and Analytical
2.Drug Substance - Quality Assurance
Quality Assurance In Process-Drug Substance Manufacturing, Upstream, Downstream
3.ASAT - Biosimilar
Analytical method transfers, analytical method validation, real time investigations, annual method performance, addressing regular queries.
4.Quality control- Lab support
To plan and execute the equipment's qualification and calibration activities. Execution of routine periodic review of GxP. As per GAMP5 and 21CFR compliance
5.Quality Control - Bioassay
Experience in cell - based bioassays, SPR Techniques, FACS techniques.
6.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.
7.Quality Control Associate Analytical
Perform analysis in laboratory for the biosimilar /biologics Products, perform chromatography techniques like RP-HPLC, Glycan, SEC, IEX, pep map
8.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.
C.Hiring for Manufacturing Roles
Experience Required: 3 to 10 years
1.Team Member - Packing
Skill in medical device packaging and visual inspection with expertise in strategic planning, documentation, aligned with cGMP standards
2.TM Engineering - Drug Product / Sterile/Injectable (I&A)
Instrumentation & Automation: Automation Platforms Vial Filing, Washing, Tunnel
3.TM Engineering - Drug Substance Mechanical
Instrumentation & Automation: Automation Platforms ABB800xA, Siemens, Allen Bradley PLCS, SCADA system, Biopharma Equipment's (Bioreactors, TFF, ATF) cGMP & QMS
4.Team Member - Drug Substance Upstream / Downstream
Execute Downstream/Upstream unit operations, ensuring documentation and compliance within GMP (Good Manufacturing Plant)
5.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
How To Apply: Click Here For Apply
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| Dr. Reddy’s Walk-In Interview For Quality, Manufacturing and R&D Departments |
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