M.Sc

Post Graduate Degree in Pharmaceutical Sciences, Bio-Chemistry, Biotechnology, Chemistry, Pharmacology, Microbiology from a recognized University. or equivalent Associate-ship diploma of the Institution of Chemists; experience in Chemical/Physio-chemical testing and analysis of drugs in drugs testing laboratory under the Drugs and Cosmetics Act and Rules.

Basic & Translational Research in Cancer; Post graduation in M.Pharma, Life Sciences, Biotech, zoology, Botany with PG Diploma in Clinical Research-Mandatory. To work on project entitled Basic and Translational Research in Cancer.

Project entitled Development of human iPSCs derived 3D lung organoid as a model for Idiopathic pulmonary fibrosis disease : A potential preclinical platform for screening of anti-fibrosis drug and novel biomarker discovery. M.Sc. in Life Sciences, Biotechnology, Biochemistry, Molecular Biology

M.Sc. Biotechnology, Microbiology or relevant life sciences discipline with a minimum of 55% marks. Minimum experience of two years as researcher. Establishment of synthetic antibody engineering platform for rapid development of indigenous bispecific antibodies to debilitate zoonotic pathogens reducing their pandemic potential.

M.Pharm, MS Pharm, MSc or Equivalent with specialization in Biotechnology, Microbiology or Life sciences. Investigating of the role of LncRNA PANDAR in the progression and metastasis of ovarian cancer. Prior experience in basic techniques in Molecular Biology, Cell culture and Biochemistry are desirable but not mandatory.

Comprehensive sero-profiling post Ivermectin, Diethylcarbamazine and Albendazole administration: Designing endpoints for Lymphatic Filariasis elimination. M.Pharm., M.V.Sc., or equivalent degree with high academic attainment and at least two years research experience after M. Sc. etc.

Through our in-house R&D and licensing, Cronus brings several differentiated generic products serving the companion, equine and production animal markets.

Perform and review method validation of Assay, Dissolution, Related compound and Residual solvents etc. Preparation of method validation/verification protocol.

Monitoring and ensuring timely completion of GLP studies. Impurity profiling - structure elucidation of unknown impurities. Supporting the team to develop the methods on HPLC, GC, IC, ICP-MS, GC-MSMS and LC-MSMS