largest lyophilized injectable plant, Gufic Biosciences. B.Pharma / M.Sc, Preference will be given to the candidates having experience of working in sterile pharma plant.
To audit all laboratory worksheets, calibration protocols/reports and raw data archives to ensure the validity and accuracy of the data. M.Pharmacy, B.Pharmacy or M.Sc or B.Sc Life Sciences at Virchow Biotech
26 positions for Scientist - Non-Medical at ICMR. Masters from a recognised university in Pharmacy Pharmacology OR Pharm-D degree recognized by UGC / PCI
Ph.D. in Biotechnology/Microbiology/Life Sciences or related fields. M.Pharm / M.S(Pharm) / M. Tech (Pharm) / M.Tech in Pharmaceutics / Pharmacology and Toxicology / Pharmacology / Pharmaceutical Chemistry with GATE/GPAT/NET.
Ph.D. or equivalent degree in relevant discipline from a recognized university. The award of Associate-ship will not confer any right on the candidate for further employment in DRDO. Director, DMSRDE reserves the right not to select any candidate, if suitable candidates are not available.
Hands-on experience/expertise in processing, analysis, and biological interpretation of untargeted metabolomics and lipidomic datasets using proprietary and freely available software tools such as MetaboAnalyst, MS-DIAL, LipidXplorer, OpenMS and or related platforms.
To facilitate the Change Controls to be logged for various reasons. To initiate the Change Controls due to revision in BMR / BPRs and other PD related changes
Lead and guide the team for TPM Operations and functionality on GMP aspects and Abbott policies and procedures, though site visits and ensure an audit readiness of sites.
Lead teams to drive technical excellence and analytical problem-solving. Handle impurity profiling, degradation studies, structure elucidation, and method validation.
Gufic Biosciences Ltd is a leading pharmaceutical industry since 1970 and is one of the world’s largest Lyophilization injectables & wide range of API products, at Navsari
Prepare, compile, review, and submit product registration dossiers in CTD I eCTD format as per country-specific requirements and EAEU Unified Registration Procedure.