Scientific/technical documents drafting, patents. Interact with R&D team to convert invention into IP. Legal drafting,formalities,filing, procedures, trademark search, competitor tracking Analysis, language US, EPO, JP, CN patent filing & prosecution
STR Data Analysis of micro-satellite data allele and distinguishing profile Genotypic analysis of different type of markers To work on .fsa file generated from sequencing data Adequate training would be provided
To conduct vendor evaluation activities for RM and PM. 7. Any other task assigned by Reporting Manager. 8. To review artwork related work in coordination with QC and QA deptt. Qualification- B.Sc.( Biotech)/ M.Sc. ( Biotech)/B.Tech (Biotech) Experience- 10 to 15 years Key skills: working experience
of avoiding adverse side effects of medicines launched in the market. Eligibility: Bsc / Msc : life science, microbiology, zoology, biotechnology, bioinformatics, Microbiology, Biochemistry, Biotech, Biology, Chemistry, Botany, zoology, “Environmental science”, Biomedical, Pharmacy, nursing, food & nutrition Any science, lifescience, bio science & paramedical graduates
are prepared, reviewed and approved as per approved procedure. 14. Any other task assigned by reporting manager. 15. Functional reporting shall as be per Departmental organogram. The responsibilities may be reviewed/added as per company requirements from time to time. Qualification- B.Sc.( Biotech)/ M.Sc ...
Nos. Job Location: Chandivali, Mumbai Designation: Manager Regulatory Affairs Education: B.Pharm/ M.Pharm Experience: 10-15 years experience into Pharma Regulatory Industry: Pharma/ Biotech Function Area: Regulatory Affairs Key Skills: ROW, CTD, ACTD, pharma regulatory affairs, RA, manager, Please refer the given job description for detailed information