About USP:
Jobs and Obligations
Lines up with USP's central goal, objectives and targets and follows USP's rules and different necessities.
Shows research facility abilities and hands on aptitude in logical Chromatography (HPLC/UPLC/Particle chromatography), Slim Electrophoresis, SEC-MALS, Roundabout dichroism and Mass-spectrometry.
Perform Unblemished Mass, Peptide planning, Glycan profiling, HMW and LMW, HCP, Debasement Profiling studies and PTM examination
Designs and executes Compendial and Research and development projects other than contributing in the new drives viz., verification of idea reads up in Biologics for item classes like proteins, catalysts, immunizations, monoclonal antibodies, peptides, anti-toxins, and some other organic items as alloted.
Assesses and examines logical reports, applies individual experience, scholastic preparation, and specialized bits of knowledge to investigate and tackle issues in the research center inside the extension.
Performs authoritative obligations, coaches and trains colleague/individuals as appointed.
Effectively takes part in project coordination with cross-useful/worldwide groups and lines up with Worldwide Biologics targets.
Gets ready and surveys project reports, SOPs, and different archives to guarantee consistence to USP's Quality Administration Framework and contribute in ISO 9001 and ISO 17025 reviews
Helps and suggests upgrades in research center/project the executives techniques and cycles.
Performs different obligations as doled out.
Essential Capabilities
MSc./M.Tech./M.Pharm. in important stream of natural sciences with 8-12 years of industry experience working in Logical Research and development and QC division of Biopharmaceutical industry.
Experience in strategy improvement, approval and innovation move and logical portrayal for biomolecules.
Favored Capabilities
M.Sc. (Natural chemistry/Biotechnology)/M. Tech (Biotechnology/Bioprocess Designing)/M. Pharm with commonsense active experience on cutting edge methods like Mass Spectrometry, Fine Electrophoresis, SEC-MALS, Roundabout dichroism, Chromatography and Biochemical or Enzymatic Measures.
Information on reference principles improvement and cooperation connected with biopharmaceutical items (mAb, Peptide, Immunization and so forth). Experience with reference materials assembling and improvement is an or more.
The up-and-comer ought to be knowledgeable with activity and investigating of all instruments utilized in playing out the previously mentioned logical strategies and ought to have sound information on QMS frameworks.
Past experience working in biopharma cGLP/cGMP/QMS climate with viable involvement with great documentation practices would be a benefit.
The up-and-comer ought to have solid abilities in specialized composition, correspondence, and show abilities.