April 2025

Masters or Ph.D. in Biotechnology, Genomic Science, Biochemistry, Bioinformatics, Biomedical, Bioprocessing with a strong technical knowledge in the respective core domain and passion for life science-related industry segments.

The ideal candidate will have advanced Excel skills and a background in Pharmacovigilance and Safety Operations or Research and Development. This hybrid role requires rotational shifts and offers an opportunity to make a significant impact on our projects and society.

Master Degree in Science, Technology, Pharmacy from a recognized university. Collect, label, preserve, and transport patient samples blood, urine, tissue adhering to safety and ethical standards. Perform diagnostic tests across multiple disciplines and ensure proper functioning of lab equipment. 

Bharat Technology is a premier college in Howrah, West Bengal with 19 years of academic excellence. Presently we are conducting fulltime Pharmacy courses like M.Pharm., B.Pharm and D.Pharm.

This project will involve cloning, expression and purification of recombinant proteins and their biophysical characterization. Cell culture and animal model experiments. Synthesis and characterization of small molecules.

Expertise in the synthesis of inorganic and hybrid halide materials. Expertise in single crystal growth and solving crystal structure. Extensive research experience in the field of Materials Chemistry.

PhD in any branch of Science, from a recognized University, Institute. Two years of post-PhD experience in research, laboratory management including, but not limited to, writing/administering research grants.

Targeting Malaria Parasite Heme Synthesis – A New Intervention Strategy for Malaria Transmission, Liver stage Prophylaxis and Relapse . Ph.D. in Biotechnology, Life Sciences or any of the allied subjects. Research experience in cell culture techniques, transfections, and biochemistry and molecular biology experiments is required. Candidates with at least one first author research paper in peer-reviewed journal will be preferred.

Must have worked in regulated plants having approvals of USFDA, MHRA. etc. Hands-on experience in handling and implementing cGMP Current Good Manufacturing Practice practices and Good Documentation Practices

Execute Analytical method Validation activities of drug substances API by using HPLC,GC and Spectroscopic techniques as per regulatory guidelines. Execution and coordination for Analytical method transfer activities of drug substances.