Candidates with M.Sc. Biochemistry / Biotechnology / Microbiology / Life Sciences or M.Tech. Biotechnology. Candidates having Hands on experience on basic molecular biology techniques, mutagenesis, cell culture will have added advantage.

The research we do and the products we develop improve outcomes for patients around the world. As a Research Associate - F&D at Baxter, your work contributes directly to making a significant impact on others. It's exciting work and you're not on your own.

RA publishing will participate in the publishing of different regulatory activities. The focus will be to ensure 100% quality and timeline of the submission. This role will be the primary interface with the Regulatory Affairs Associate

Demonstrated experience across all phases and aspects of a comprehensive process redesign, such as data gathering, baselining, root cause analysis, quantitative and qualitative analysis, data modeling, future state design, implementation and validation of results

Masters degree in any areas of Life Sciences or Pharmacy/ Pharmacology with first class or equivalent in terms of Grades or marks at the preceding degree and excellent academic record throughout. 

B.Pharm with experience of working in Dispensary, Pharmacy of any recognized hospital OR D. Pharm with experience of working in a Dispensary, Pharmacy of any recognized hospital

M.Pharm or M.Sc in Biochemistry/ Biotechnology/ Microbiology/ Life Sciences. Towards discovery and development of novel drugs and pharmaceuticals Metastatic and Chemoresistant Breast Cancer Stem Cells

B.Pharm with experience in relevant field or M.Pharm experience in relevant field Or Pharm.D with experience in relevant field

B.Pharmacy with minimum two years Diploma in Medical Imaging Technology from State Board of Technical Education or any equivalent Diploma from a recognized Board, University.

MPharm in Pharmaceutics, Industrial Pharmacy, Pharmaceutical Technology or related discipline with experience in Novel drug delivery, Nanotechnology, Long acting Injections, HPLC, LC MS MS, cell line studies, animal studies, etc.

MSc in Biotechnology, Biochemistry, Life Science from recognized university or equivalent. Experience in development & characterization of transgenics in Arabidopsis and or other plants, protein- protein interaction studies, RNASeq analysis, etc

B.Sc / M.Sc / B.Pharma ; Having an exposure in FG analysis, Stability Analysis, AMV/AMT, GLP, Documentation in Quality Control Department; Sun Pharma

M.Sc, PG degree in Biological Sciences, Qualified in National Level Examinations conducted by Central Government Departments and Agencies, CSIR-UGC NET, GATE, DBT-BET

M.Pharm, B.Pharm, M.Sc, B.Sc ; Trouble Shooter, Granulation, Compression, Coating, Machine Operators and Executives

Masters degree or higher in Chemistry, Pharmacy; Well versed experience of all GMP systems including facing audits for EU, UK and other Regulated markets.

Amneal Pharmaceuticals, Inc. announced that the U.S. Food and Drug Administration has approved Brekiya dihydroergotamine mesylate injection, the first and only dihydroergotamine autoinjector for the acute treatment of migraine with or without aura and the acute treatment of cluster headaches in adults.

B.Pharma, M.Pharma; National Center for Disease Informatics and Research, NCDIR is one of its kind of unique institution which utilizes information science for health research as its integral component.

Support the technical team with project appraisal, technical due diligence and related organizational activities of the vertical. Project management for various programs as sanctioned. Make detailed observations, analyze data and interpret results. Monitoring & Technical evaluation of projects under various programs to meet targets.

Design and synthesis of small molecules for medicinal chemistry. Additionally, candidate should perform nucleic acid delivery and conduct preclinical animal experiments.