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.

Candidate should have experience in Oral formulations Solid and liquid for Handling of IPQA, APQR activity and Process Validation. Candidates must have experience in review of Analytical Document, Investigating out-of-specification results, and ensuring adherence to GMP guidelines.

Monitoring CAPA till completion, Management of lateness documentation form, identify the Deviation Owner, Follow-up in case of no response, Identify potential critical and major systemic deviation and escalate as required. Identify Trends during ongoing investigations and as part of retrospective reviews.

Achieve Division wise primary target and ensure it to be equal to or greater than Secondary. Generate maximum prescriptions & increase market share. Ensure zero cases of expiry on Stockist shelf by timely liquidation of stocks by prescription generation.

Engage in peer-to-peer level dialogue with key customers and deliver appropriate clinical, scientific content through utilizing the correct channel mix, which will differentiate AstraZeneca products from those of other companies.

Act as an interface with identified scientific leaders, building regional relationships to contribute to understanding diseases, research trends, clinical practice guidelines, and treatment patterns. Educate healthcare professionals about specific drugs or medical devices, answering their scientific questions and ensuring products are used effectively.

Ist class M.Sc with 5 years experience or Ist class M.Tech, MD, MVSc, M.Pharm, M.Biotech with 4 years R&D experience OR Ph.D with 4 years postdoctoral experience in the relevant field.

Candidates shall be eligible to apply for admission and registration within the ongoing program of research at IASST, if he, she has obtained 55% marks in aggregate Equivalent CGPA in 10-point scale in the master’s degree examination.

Postgraduate Degree M.D Homeopathy, Doctoral degree in Science, Pharma, MD, MS from a recognized University or equivalent. Experience in serving in cancer OPD. Wet lab molecular diagnostics, biological sample handling experience

Master Degree in Botany or Zoology or Microbiology or Biotechnology or Biochemistry or Physical Anthropology or Genetics or Forensic Science with Botany or Zoology as one of the subjects during all the three years of bachelor of Science from a recognised University or Institute.

Ph.D. Programme Admissions June - 2025 at NIBMG. NIBMG is equipped with state-of-the-art technologies which include single-cell sequencing, spatial omics and next generation sequencing platforms, robotics platforms, high-end computational and bioinformatics facility, cell and molecular biology facilities, genetic engineering including cutting-edge CRISPR-Cas genome editing laboratories.

B.Pharm OR D.Pharm. Experience in Dispensary / Pharmacy of the Hospital having minimum 200 beds.  Candidate should be prepared to work in shift duties, including night shift. Registration with State Pharmacy Council with duly allotted Registration Number is mandatory. 

Applications are invited for the post of Clinical Research Coordinator in different drug trials. The following are the educational qualifications/salary for this post.

M. Pharm Pharmaceutical Quality Assurance, Pharmaceutics, Industrial Pharmacy and Ph.D. in relevant discipline, preferably in Pharmaceutical Quality Assurance. fresh and experienced; good track record of publications, patents, grants