To be an integral part of an antibody development team with a focus on performance and improve customer outcomes through validation of cell culture workflows, reagents, and consumables.
Ph.D. in Pharmaceutical Technology Formulations, Pharmaceutics, Industrial Pharmacy with M.Pharm, M.S Pharm in Pharmaceutical Technology Formulations, Pharmaceutics, Industry Pharmacy. At least one research paper in SCI indexed journal.
To be an integral part of an antibody development team with a focus on performance and specificity using innovative molecular, protein, and cell biology methods.
PhD in biological sciences, preferably infection biology. Prior experience in working with infectious agents and biological specimens Excellent written and verbal communication required with exceptional organizational skills
This is a non-supervisory position in Reference Standard Laboratory responsible for performing the required tests as part of the project and maintaining the GLP environment in the Laboratory. The incumbent will utilize his or her technical expertise, knowledge of pharmaceutical analysis in collaborative testing, efficient and effective laboratory operations.
Project Name Strengthening genomic surveillance for vector borne diseases in India. Post Graduate Degree Virology, Microbiology, including the integrated PG degrees with PhD.
Ph.D. in Health Sciences with first class or equivalent grade at the preceding degree M.Pharm, M.S, M.Sc, M.D in Pharmacy Practice, Clinical Pharmacy, Clinical Pharmacology, or Clinical Epidemiology with a very good academic record throughout with 2 years of Teaching, Research, Industrial experience with published works of high quality.
PhD in Computer Science, Computational Biology, Bioinformatics or related discipline with application of the above-mentioned skills. Demonstrated experience in development of software tools and data analysis pipelines.
Qualified to degree level in biosciences or an equivalent healthcare or pharmaceutical industry background, with proven competency in patient safety pharmacovigilance/clinical development.
Develop, optimize, and publish high-quality analytical methods using high-field NMR and qNMR applications; publications may include white papers, application notes, or journal articles ; Acquire high resolution qNMR spectra and implement structural elucidation for obtaining chemical structural information to develop QM spectral analysis models