M.S. Pharm, M.Pharm, M.Tech Pharm. MD Pharmacology , MVSc. Pharmacology, Pathology, Biotechnology with a minimum 60% aggregate or 6.75 CGPA. Candidates who have qualified CSIR-NET, UGC-JRF, GATE will be preferred.
Vivo Bio Tech is a full service Pre-Clinical CRO offering drug development & discovery services to pharmaceutical & biotech companies world-wide in accordance with OECD - GLP, AAALAC & IND guidelines. The company offers services in the areas of In vivo & In vitro toxicity studies, Pharmacological investigations, Pharmacokinetic & toxicokinetic studies, Genotoxicity screening, Analytical services etc. Our experienced & skilled talented scientists offer advice on defining drug development paths tailored to specific molecules.
Review of technology transfer documents and initiate the validation accordingly in plant scale by coordinating with CFT. Review of Master Batch Manufacturing records executed Batch manufacturing records.
Ph.D. degree in life sciences or biotechnology equivalent from a recognized university with four years of post-qualification experience in the protein or vaccine development industry. OR MSc degree in Life Sciences or B.Tech degree in Biotechnology or equivalent from a recognized university
Masters degree in Bioinformatics, Biotechnology, Computational Science, Pharma or equivalent with one year of post qualification experience in the relevant field.
AIIMS Jodhpur is one of the SIX NEW AIIMS established by the Ministry of Health & Family Welfare, Government of India under the Pradhan Mantri Swasthya Suraksha Yojna (PMSSY) with the aim of correcting regional imbalances in quality tertiary level healthcare in the country and attaining self sufficiency in graduate and postgraduate medical education. PMSSY planned to set up 6 new AIIMS like institutions in under served areas of the country.
Bachelor or Master degree Biotechnology, Pharmacy, Science or Ph. D Biotechnology, Biological Sciences or equivalent.
Minimum 3-5 Years of experience in Pharmaceutical Industry with major experience in Regulatory Sciences group handling new submissions and, or LCM submission to global health authorities especially USFDA, EMA and other EU authorities.