Scientist

Ph. D thesis submitted in Microbiology, Life sciences in the area of basic and applied microbiology from a recognized University. 

Analytical Development Scientist-I with some supervision from the Analytical Development Lead focuses on the analysis of route scouting and Chemical Process Development of Bayers existing and pipeline crop protective agents. Collaborates with all internal and external functional teams.

The WISE-IPR programme a programme of the Department of Science and Technology offers training in different fields of Intellectual Property Rights. This one- year training programme provides theoretical knowledge of IPRs as well as on-the-job training at various centers in the country.

Hands on experience in physicochemical characterization, solid state characterization, polymorph screening and salt screening techniques is must. Should have good knowledge on industrial crystallization procedures and drug substance manufacturing process.

Personnel handling this profile will be responsible for performing reactions as per the requirement of the project. They are also responsible for documenting the observations in relevant note books.

Master of Public Health with Bachelor of Dental Surgery. Or Master of Pharmacy. Minimum one year of relevant experience in public health research.

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.