The Technical Consultant will work as a Project Manager, driving implementation of key schemes including the Departments Production Linked Incentive schemes by effectively liaising between the Project Management Agencies, scheme participants, the Department of Pharmaceuticals in the Ministry of Chemicals and Fertilizers, and the other Ministries, Departments of the Central Government and State Governments concerned.

A Phase 3, Multicenter, Open-label, Rater-blind, Active-controlled Study to Evaluate the Efficacy and Safety of Bedaquiline for the Treatment of Multibacillary Leprosy When Combined with Rifampicin and Clofazimine.

Ph.D. in any branch of Life Sciences. Prior experience in molecular biology techniques, cell culture assays, expression and purification of proteins, and cellular signaling are required. Hands-on experience with X-ray crystallography or cryo-EM is preferred but not essential.

M.Sc. in any branch of Life Sciences. Prior experience in molecular biology techniques, cell culture assays, expression and purification of proteins, and cellular signaling are required.

Analysis and processing of In process and Finished product and handling of HPLC, UV, FTIR, K/F, AAS, IC, Dissolution. Analysis of Raw material and Excipients and handling of HPLC.

The candidate will be responsible for preparation and submission of dossiers for NCEs and NBEs and will present it to relevant internal and external stakeholders. The candidate will represent the company with Indian regulatory agencies, including CDSCO, RCGM, Central Bureau of Narcotics and Karnataka drugs control department.

After a journey of growth spanning 27 years as Cadila Healthcare Ltd. and the Zydus Group, we have evolved and transformed ourselves in response to the changing times.

Centaur Pharmaceuticals one of the rapidly growing Pharmaceuticals Company in India. Centaur Pharmaceuticals is USFDA and MHRA approved plant is seeking deserving candidates having experience working in Oral Solid Dosage Manufacturing facilities for regulatory market's.

Plan, execute & ensure timely submission of various applications when assigned including but not limited to only these: test license application, HAQ response submission, CT updates and notification submission e.g. IB amendment, site closure, site addition, EC approval submission etc.

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.