Projects

Doctoral Degree in Science, Engineering, Technology, Pharma, MD, MS from a recognized University or equivalent. CSIR-Centre for Cellular and Molecular Biology, Hyderabad is a premier Research Institute under the aegis of Council of Scientific & Industrial Research, an autonomous body under the Ministry of Science & Technology, Government of India.

M.Pharm or M.Sc Chemistry, Analytical Chemistry, Medicinal Plants, Phytochemistry from a recognized University, Institute. engagement of project staff in the programme Management Unit of Regional Raw Drug Repository of Trans Ganga Plain Region

Pharm.D from an institution approved under section 12 of the Pharmacy Act, 1945. Essential 3 years experience in teaching, research, regulatory, hospital pharmacy, out of which preferably 1 years shall be in a responsible administrative position.

Design and development of lipid- based nanoparticles for the delivery of levonorgestrel through umbilical skin tissues to prevent pregnancy.

First class M.Sc in Biological Sciences, Biotechnology, Pharmaceutical Sciences, Chemistry. Applicant must be qualified in any one of the following tests CSIR, UGC, ICMR including Lectureship Assistant Professorship OR GATE. National Level examination DST, DBT, MoE, ICMR, IIT etc.

M.Sc in Life Sciences with 60% marks. Experience in Molecular Biology techniques, Isothermal DNA amplification method and Cloning. Development of new molecular assays for the detection.

First class M.Sc any field of Life Science Applicant must be qualified in any one of the following tests CSIR, UGC, ICMR including Lectureship Assistant Professorship OR GATE. National Level examination DST, DBT, MoE, ICMR, IIT etc

Masters Degree in Life Sciences, MVSC, Engineering or Medicine from a recognised university or equivalent With at least 1 years of R&D experience in academic institution or relevant industry with NET & GATE Hands-on experience in cell culture

M.Pharm, M.Sc, Pharm.D candidates who completed a Diploma course in clinical research and with at least three-year experience in handling clinical trials