Design and synthesis of small molecules for medicinal chemistry. Additionally, candidate should perform nucleic acid delivery and conduct preclinical animal experiments.
The department is responsible for evaluation and screening of proposals, grants and funds management, ensuring the growth of biotechnology innovations and fostering a collaborative approach toward addressing challenges in sectors like healthcare, agriculture, and environmental sustainability.
The candidates should mandatory have extensive experience through their PhD or other trainings in working with transplantable or inducible mouse models of cancer, and be well-versed in multi-colour flow cytometry. The candidates should be well-versed with regular laboratory techniques, which include but are not limited to western blotting, Immunohistochemistry, qPCR, etc
To carry out day-to-day lab research activities in the lab. Self-driven candidates interested in infectious disease research and with experience in parasitology, imaging, Molecular Biology, entomology and mosquito infection research are preferred.
Prepare and review continued process verification reports for ongoing commercial products and communicate risks for taking appropriate measures for mitigation. Maintain timeline for completion of the reports along with approval.
Knowledge of handling SCADA base coating machine. Knowledge of equipment in granulation and able to handle Integrated Granulation Line PLC based equipment
Responsible for Monitoring and Completion of the production batches as the scheduled timelines. Responsible for implementation of the cGMP practices in the area. Responsible for Indenting of the production process related accessories and consumables.
Candidate should have experience in - Executing CAR-T cell production at lab scale and / or clinical / commercial scale including isolation of T cells, activation and transduction etc.
Supervise production team operations. Handle equipment: Sifter, FBD, Dryer, Centrifuge, ANF, Spray Dryer, Reactor, etc.
Ensure compliance with GMP processes. Maintain BMR, BPR, and logbooks.
B.Pharm / M.Pharm / M.Sc. ; Handling of complex injectable products and peptide molecules analysis. Core competency to take care of CMO, CDMO products. Ownership on Testing and compliance.