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| Job Location | Navi Mumbai |
| Education | Not Mentioned |
| Salary | Not Disclosed |
| Industry | Pharma / Biotech |
| Functional Area | General / Other Software |
| EmploymentType | Full-time |
JOB DESCRIPTION:Roles & Responsibilities: -Downstream Process development of Equine Biologicals & Human Biologicals-including Chromatography Gel Validation studies, Execution of PDR experiments. -Scale up of the processes from lab scale to manufacturing scale -Tech transfer of Equine Biologicals & Human Biologicals. -Development of high yield, high purity new generation purification processes. Documentation: -Preparation of Documents -Such as MMF, Study protocol, PDR, Chromatography Gel Validation, -Timely completion of Lab logbooks, BMRs for internals & external audits. -Preparation of BMR, SOP, URS, Study protocol, Study report, Data compilation -Execution of Non GLP & GLP Virus validation studies -Co-ordination with QA, QC, Production, Horse farm (Antigen & Plasma), Engineering department. Unit operations: -Hands on Experience on handling of Unit operations -Precipitation, Ultrafiltration, Column chromatography , Nanofiltration, Lyophilization Additional responsibilities: -Ordering & maintenance of Chemicals, materials, reagents, stocks on regular basis. -Training of staff and overseeing general lab activities -Sound knowledge of SEC HPLC, SDS PAGE, Protein content estimation-Lowry, Biuret testing ,
Keyskills :
researchdocumentation validationapi hplccontinuous improvement facilitation high yieldgeneral lab