Having Experience in Environmental Monitoring, Water Testing, In process Sampling, Analysis of Bulk Water, Finished and API by MLT, Bioburden, BET, Sterility, PET and Antibiotic Assay.

To handle all kind of lab instruments and experience to perform AMV and Documentation EM Monitoring, Water testing. Trend preparation, Microbial Testing, SOP and Protocol and other micro related activity

M.Sc. in Organic Chemistry, Analytical Chemistry Or M.Pharmacy in Pharmaceutical Analysis. Experience on the analysis of small organic molecular using various analytical techniques such as HPLC, MS, etc.

Masters in Pharmaceutical Science, Pharmaceutics, Pharmaceutical Technology, Industrial Pharmacy, Analytical Chemistry, with First class or equivalent grade at the preceding degree B. Pharm, B.Sc with a good academic record throughout. The CoE will primarily focus on the development and research of Novel Drug Delivery Systems (NDDS), creating a collaborative platform where academic expertise and cutting-edge research converge to drive innovation in this critical area of pharmaceutical science.

Post graduate degree in any branch of life sciences, biotechnology or Graduate, Post Graduate in any branch of life sciences or biotechnology or Post Graduate in any branch of life sciences, biotechnology selected through National Eligibility Tests-CSIR UGC NET including Lectureship and GATE.

Post Graduate Degree in life sciences OR Graduate, Post Graduate degree in professional course. M.V.Sc, M.Tech, MSc. Degree in Biotechnology Biochemistry, Microbiology, Immunology.

B.Pharm / M.Pharm; To perform equipment qualification, utility qualification activity with proper documentations. To perform Computer system validation. To investigate deviation, change request, OOS, market complaint etc.

Create and review regulatory documentation for Drug, Device and Combination product renewals and other life cycle maintenance-related submissions. Track status and progress of regulatory documentation.

Masters Degree in Biotechnology, Microbiology, Biochemistry, Life Sciences, Botany, Plant Science from a recognized University or equivalent. Understanding the molecular mechanism underlying seed-anociated endophytes regulated seed germination process of Himalayan medicinal plants and their application in food crops as synthetic microbial communities for stress tolerance

Diploma course in Pharmacy from an institution recognized by Government of India and the Pharmacy Council of India. Must have registered with Assam Pharmacy Council and should possess valid professional Pharmacist License. 

M.Sc. Degree in Clinical Trial abd Research, Pharmacology, Biostatistics, Biochemistry, Pharmaceutical Sciences or or equivalent qualification from a recognized University, Institution OR M.Sc. Clinical Research with experience in teaching, research in niversity, college and or research experience at equivalent level with at least 3 publications in National, International Journals 

B.Pharm or D.Pharm and registered as pharmacist under the Pharmacy Act Act 1948. Min 3 years work experience.

M.Sc, Integrated M.Sc. in Botany, Biotechnology, Microbiology, Biochemistry, Bioinformatics, Life Sciences or B.Tech. in Computer Science from recognized University.

Work on research project entitled Engineering hybrid biological systems for self-sustainable treatment of persistent mobile chemicals in common effluent treatment plant wastewater funded by Gujarat State Biotechnology Mission, Govt. of Gujarat at Gujarat M.Sc Biotechnology, Microbiology, Biochemistry or relevant life science discipline with minimum of 55% marks. Biotechnology University.

Candidates having M.Sc. or an equivalent qualification in Life Sciences or related subjects Biotechnology, Biochemistry, Genetics, Microbiology, Bioinformatics with a minimum of 60% marks or an equivalent grade point relaxation will be as per Govt. guideline are eligible to apply.

Post-graduate degree in Basic Sciences or Professional Courses. Candidates with 1-2 years of hands-on experience in mammalian cell culture, stem cell culture, molecular biology, RNA isolation/western blotting, FACS, microscopy imaging techniques are preferred. Those with experience in zebrafish and mouse model may also apply.

Lab Exposure, Analytical Method Validation. Review of Specification. Method of Analysis Protocol Handing of 00S and 00T. Investigation and Lab event. Review & Approval of QC Documents. Knowledge of Qualification and Validation related Activities. Audit Trail Review etc 

Experience in pharmacovigilance, in clinical care, or in clinical or scientific research is an advantage but not a requirement. Demonstrated computer literacy, particularly in the use and management of relational databases.