Dr. Reddy’s Biologics enable access to high-quality, cost-competitive biosimilars. The future we imagine is one where patients worldwide find ease in illness, every day. Our state-of-the-art manufacturing facilities and end-to-end capabilities bring this future within reach making us a leading biosimilars manufacturer.

Career-Expo in Ahmedabad

Team Member – Packing 
Skill in medical device packaging and visual inspection with expertise in strategic planning, documentation, aligned with cGMP standards

TM Engineering – Drug Product / Sterile/ Injectable (l&A) 
Instrumentation & Automation: Automation Platforms Vial Filing, Washing, Tunnel

TM Engineering – Drug Substance Mechanical 
Instrumentation & Automation : Automation Platforms ABB800xA, Siemens, Allen Bradley PLCs, SCADA system, Biopharma Equipment’s ( Bioreactors, TFF, ATF ) cGMP & QMS

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

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 GAMP5 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 / biologies 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.

Additional Information
Experience : 3-10 years
Qualification : Diploma/ B Tech, B.sc, MSc, B.Pharm, BTech or Masters in Biotechnology / Microbiology /Biochemistry
Location : Bachupally / Shamirpet Hyderabad

Walk in Interview
Date : 9th November, Sunday
Time : 9:00 am onwards
Venue : THE FERN RESIDENCY
Near Subhash Bridge Corner, RTO Circle Ahmedabad Gujarat 380027

Interested candidate should apply online : Click here