PhD degree in Molecular Biology, Genomics or equivalent and handling of modern analytical instruments. Masters degree in Microbiology, Molecular Biology, Genomics or equivalent with Minimum 3 Year experience in handling of modern analytical instruments.
Ph.D. in Biotechnology, Bioinformatics, Biochemistry, Life science or equivalent degree OR 2. Having 3 years of experience in research design and development after M.V.Sc, M.Tech in Biotechnology, Biological Sciences, Bioinformatics, Life Sciences, Molecular Biology with at least one research paper published in Science Citation Indexed
This is a hands-on, non-supervisory, non-laboratory role in the India Biologics department. The incumbent will support the reference standard program within the Global Biologics department. The incumbent in this role will focus on supporting the suitability program, including preparing and reviewing CSU testing protocols, providing technical assistance to testing labs, reviewing analytical data and preparing summary reports to assist in confirming the continued suitability of USP Reference Standards.
Women Scientists having Post-Graduate Degree in Basic, Applied Science or equivalent degree like M. Phil., M. Tech., M. Pharm., etc. or B.Tech. are eligible for WISE-PhD.
Masters Degree in Life Sciences, MVSC or Bachelors degree in Engineering or Technology or Medicine from a recognised university or equivalent. Four years experience in R&D in industrial or academic institutions or science and technology organisations.
A professional with MD or PhD Bioinformatics from recognized institution. The ideal candidate will have experience in handling and analysing Next-generation sequencing data.
The candidate must possess a thorough understanding of relevant disease biology, the clinical landscape, emerging technologies, and the competitive environment.
Must have hands on experience in working with chemical methods and handling instruments like Prep HPLC and HPLC. Expertise in HPLC & Prep HPLC method development and basic undersatnding in data interpretation of various analytical technique such as LCMS, GCMS, FTIR, UV-Visible, NMR etc is required.
Skilled scientist with expertise in trace level quantification of GTI/ Nitrosamines/Nitrites or similar impurities using LC-UV/FID, Ion chromatography and LCMS. Ensure all own activities are aligned with overall drug development process. Work according to appropriate SOPs, GMP, GLP, QM, HSE, ISEC & Novartis Guidelines; Strategic and scientific contribution to Networks, target achievements according to net-work charter and annual objectives