Scientist In Drug Product Attributes (dpa- Ms) Group Job in Dr Reddys Path Labs Private Limited

Job Description:

Key Responsibilities :

Hands on experience of QTOF, other HRMS and TQ LC-MS techniques. Complete, in-dept knowledge on Biosimilars characterization (Intact mass analysis, peptide mapping, PTM analysis, etc.) using LC-MS/MS. Knowledge on spent media analysis using TQ LCMS Experience on method development and qualification for various mAb s suing LC-MS/MS. Characterization of SSR/Signal peptide Knowledge on ICH guidelines To ensure implementation of SHE and QMS at work place. To draft the study protocols, method development reports, comparability reports and CMC sections of regulatory documents Maintenance of laboratory as per the cGLP. Having the good writing, presentation and documentation skill Understanding on good laboratory practices and Good Documentation Practices. Education & Experience: M. Pharm / MSc with minimum 8-10 years of working experience Method development, qualification, Handling of analytical instruments like HRMS, TQ LCMS, Synapt, Xevo QTOF, etc