Biotechnology

Post Graduate degree in Life Science, Pharmacy, including the integrated PG degrees. Candidate with a Ph. D degree with specialization in Pharmaceutics, Pharmacology and Toxicology, Biotechnology, Life Sciences, Pharmacy and or significant experience in the formulation and development of nanotechnology-based drug delivery systems, clinical research, In vitro and In vivo models and molecular biology. 

The candidate will be responsible for performing a range of wet-lab based analyses, which include routine semen analysis, sperm DNA Fragmentation Index assessment, Y-chromosome microdeletion testing, RNA extraction, DNA extraction, protein extraction, PCR analysis, and ELISA assays. These tasks will be carried out as part of the broader study objectives, ensuring high standards of accuracy and consistency.

M.Sc in Plant Biotechnology, Biochemistry, Botany, with Three Years Research Experience OR Doctoral Degree in Biotechnology, Biochemistry, Botany. Experience of working in plant tissue culture and transformation, molecular biology techniques and plant genome editing.

The Manager Drug Safety Content Analysis will manage and supervise project’s PV Operations/training staff on a day-to-day basis, guiding performance of PV Operations staff in ongoing projects in terms of training, quality of deliverables, compliance with the timelines and relevant trainings.

handle R&D projects independently in the areas of epidemiology, big data analytics, drug/ target/ biomarker discovery, preclinical and clinical evaluation of medical devices, IVDs, therapies, vaccines, field feasibility studies of the novel interventions, and experience/ exposure to regulatory aspects of health technologies, IP protection, Technology transfer. Health policy development and implementation. MD, MS or equivalent degree recognised by MCI, NMC OR MBBS or equivalent degree recognized by MCI, NMC, with MPH from a recognised university OR M.Sc or MBBS or equivalent degree, recognised by MCI, NMC, with Ph.D. from a recognised University.

Write brief narratives summarizing the ICSR criteria and other potentially safety-relevant information in each article. Demonstrates understanding of client’s drugs labels and uses that knowledge effectively when performing the safety assessments.

PhD, MD, MS, MDS in Biochemistry, Biotechnology or an equivalent degree. OR Having 3 years of research, teaching, and design and development experience after MVSc, M.Pharm, ME, M.Tech with atleast one research paper in Science Citation Indexed Journal. 

Development of a nanostructured graphene oxide, polydopamine coated PDMS nano-biosensor monitoring GPC1 for the early diagnosis of pancreatic cancer.

Identification of key regulators and their controlling Mechanism in a combinatorial amyotrophic lateral sclerosis Network : an integrated bioinformatics analysis. Experience in computational tools, Network Biology, Molecular modeling and Simulation, Knowledge of computer programming languages with good command in oral and written communication skills in English will be given preference.