R&D

Essentially good academic record with First Class M.Sc, M.Tech with a minimum 60% marks or equivalent CGPA in aggregate in Biotechnology, Biochemistry, Molecular Biology, Life Sciences, Zoology. Two years of research experience for M.Sc. Candidates as evidenced by publications in peer-reviewed journals. 

HPLC, GC, IC method development, Validation and Transfer for API, complex OSD, complex generics products like long acting injectables, nasal sprays, peptide injections, peptide OSDs, oncology and Topical products etc using various analytical technique. Expertly in peptide characterization. Well versed with USP/EP/BP/IP and various current regulatory guidelines ICH/ EMEA/ FDA Hands on experience on Nitrosamine and Genotoxic impurities method development, M.Pharm / M.Sc

Development of antibiotic nano formulation for the prevention and treatment of udder infection in dairy animals. First class in M.Pharm with specialization in Pharmaceutics, Drug Delivery Technology, Pharmaceutical Technology or equivalent from a recognized University. GPAT. GATE. NET qualified.

Centre of Excellence on Phytopharmaceuticals and Herbal Products; Ph.D. in Pharmaceutical Sciences or Analytical Chemistry, Pharmaceutical Analysis with first class post- graduation in M.Sc. Analytical Chemistry, Organic Chemistry or M.Pharm, MS.Pharm Pharmaceutical Analysis, Quality Assurance, Natural Products, Medicinal Chemistry; Hands on experience for operation and analysis of HPLC and different chromatographic instruments.

Pragmatic strategies for the delivery of phytodrugs across BBB through plant derived exosomes for the management of neuroinflammatory diseases. Experience mammalian cell culture, toxicological assessments, molecular techniques PCR, Western Blotting, immunoassays, and neurodegenerative disorders preferred. Knowledge of animal handling, and neurobehavioral techniques like Open field and Morris water maze also preferred.

In this role, the Senior Scientist-I will work on isolation, purification of known and unknown impurities, compounds by preparative HPLC and characterization of molecules using various analytical technique. Prepare, execute, and complete IQ/OQ/PQ of new instruments. Indent the required glass ware, chemicals, and columns for the ARD projects.

Clinical Trial Project Manager Associate leads the cross-functional study team in the development and execution of clinical trials and is accountable both regionally and globally to deliver trials with quality, on time, and within scope and budget. Leverage scientific and regulatory knowledge to prepare and/or provide technical consultation for clinical and regulatory documents, prepare for meetings with regulatory agencies

The recruited candidate will perform majority of experiments proposed in the study, which includes preparation and characterization of nanoparticles, in vitro and in vivo safety and efficacy analysis etc. The Project Research Scientist-I will also take care of consumables ordering, storage and maintenance. The candidates with M.Sc., qualification shall enrol for Ph.D programme.

Candidates with research experience in tumor immunology, cancer biology with a proven hand in animal handling, animal animal-related experiments as evident from the original research publications will be preferred.