Biophore, an established pharmaceutical company, is engaged in the development and manufacturing of niche pharmaceutical products for the generic industry. Within a decade since inception in 2007, Biophore has emerged as a trusted partner in the generic industry across US, Europe and other regulated markets.

Pass in Pre Degree, Plus Two or equivalent. Diploma in Pharmacy conducted by the State Govt, or Central Board of education. Pharmacy Council Registration.

D.Pharm Siddha or Integrated Pharmacy course for certificate issued by Government of Tamil Nadu only.

Master’s Degree in Chemistry or Pharmaceutical Chemistry or Pharmaceutical Analysis, Quality Assurance from a recognized University or equivalent. Working expertise in HPTLC, HPLC, ICP- OES and Plant based Drug Standardization, Analysis of Aflatoxin & Pesticide residue. Skills of drafting and editing of scientific documents, technical reports

Candidates having prior experience in plant-soil- microbial interactions, soil microbiology and microbiome analysis metagenomics, microbial screening, cultivation, characterization and enrichment studies, pathway/mechanisms analysis, microbial consortia development, state-of-the art molecular biology techniques, and detection of xenobiotics and secondary metabolites, LC-MS, GC- MS are encouraged to apply. 

M.Sc, Microbiology, Biotechnology, Zoology, Botany from a recognized university or M.Sc. in life Sciences, Zoology, Botany, Marine Sciences, Chemistry, Environmental Sciences from a recognized university or equivalent.

Ph.D Biotechnology, Biochemistry, Bioinformatics or relevant branch of biological sciences with at least 1 research paper in Science Citation Indexed Journal.

Post Graduate Diploma in Clinical Trials or equivalent with at least 60% marks. At least one-year experience in clinical research. Experience in recruiting patients in clinical trials, familiarity with good documentation practices and good clinical practices.

All the full-time Ph.D. students admitted into the Ph.D. program will receive fellowship up to a maximum of five years. The fellowship could be from the Institute or Sponsored Projects. Ph.D. students may also have their own fellowship if qualified through UGC/CSIR NET.

Ability to conceptualize and drive large-scale marketing strategies with an execution-first approach. Experience in leading teams, collaborating with sales, and driving prescription demand at a national level.

Handling and Execution and investigation of QMS documents in change controls, deviations, and CAPA. Review of Analytical Method Validations, Method Transfers, Protocols & Reports. Experience in review of HPLC, GC, LCMS calibration data & Analytical Data review. 

Innovent Biologics, Inc , a world-class biopharmaceutical company that develops, manufactures and commercializes high quality medicines for the treatment of oncology, cardiovascular and metabolic, autoimmune, ophthalmology and other major diseases, announces that the first participant has been successfully dosed with IBI354

Diploma in Pharmacy D.Pharm or Bachelor of Pharmacy B.Pharm or Doctor of Pharmacy Pharm.D from a recognized University, Institution. Should be a registered Pharmacist under Pharmacy Act 1948.

Research experience in Drosophila genetics and epigenetics will be preferred. Masters degree in Natural or Pharmaceutical sciences and Three years of experience in Research and Development in industrial and academic institutions or Science and Technology organizations and scientific activities and services.

Project management for CoE-Antiviral and Antibacterial Drug Discovery and Development project and timely submission of progress reports to Director and nodal ministry. Proactively coordination of the project with various stakeholders and Principal Investigators of the project. 

Doctoral Degree in Science, Engineering, Technology, Pharma from a recognized University or equivalent; Experience in Research & Development in Industrial & Academic Institutions or Science and Technology Organizations and Scientific activities and services

Experience of conducting and writing Systematic Reviews and Meta-analysis minimum two published systematic reviews as lead author. Knowledge about GRADE methodology. Experience in Statistics and Epidemiology 

Hands-on experience in DNA sequence data analysis from FASTQ files, particularly on Human genomic or Metagenomic samples using standard data analysis pipeline. M.Sc / M.Tech in Life Science or experience in bioinformatic analysis of genomic/meta genomic data or Ph.D.in Life Science