2-3

Execution of upstream and downstream production batches. Focus on timely execution, to ensure that the process is carried out as per cGMP compliance and batch timelines

Ciron has carved a niche for itself in the sphere of operations of manufacturing Ampoules, Vials, Eye / Ear / Nasal drops, Lyophilized products and Lyophilized bulk.

Hands on experience of chromatography technique, Protein Purification, Centrifuge and Filtration.

Method development, Method Validation and routine analysis in Orals and Non-orals Formulations.

Perform site feasibility, identify potential investigator, negotiate study budget with potential investigators, finalization of investigators, sites, and execution of CDA and study-related contracts, Clinical Research Associate at Sun Pharma

M.Sc / M.Pharma; Audit facilitating and compliance report preparation. Ensuring Compliance in Production, Warehouse, Engineering facility and QC lab. Daily Plant Round for compliance monitoring.

Knowledge of global and regional pharmacovigilance regulations. Experience in Pharmacovigilance, data management, and adverse event reporting and processing, with proficiency in relevant software tools.

Design, execute, develop, and optimize upstream process for biosimilars monoclonal antibodies, fusion proteins in CHO Cells. R&D USP Mammalian, R&D Analytical, R&D Bioassay

Bachelor degree in Pharma or Life Science. pharmaceutical sales experience, preferably with diabetes products. Consistent record of meeting or exceeding sales targets