Deputy Manager
Production Management Plan, coordinate, and supervise daily API manufacturing activities in line with the approved production plan. Ensure timely execution and completion of batches as per BMR/BPR,
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Production Management Plan, coordinate, and supervise daily API manufacturing activities in line with the approved production plan. Ensure timely execution and completion of batches as per BMR/BPR,
Production Management Plan, coordinate, and supervise daily API manufacturing activities in line with the approved production plan. Ensure timely execution and completion of batches as per BMR/BPR,
Execute API manufacturing processes as per approved BMR, SOPs, process parameters, and production schedules. Supervise day-to-day production activities including charging, reaction, heating/cooling,
Plan and execute daily API manufacturing activities according to the approved production plan. Supervise manufacturing operations such as raw-material charging, reaction, heating/cooling, extraction,
Execute API manufacturing processes as per approved BMR, SOPs, process parameters, and production schedules. Supervise day-to-day production activities including charging, reaction, heating/cooling,
Plan and execute daily API manufacturing activities according to the approved production plan. Supervise manufacturing operations such as raw-material charging, reaction, heating/cooling, extraction,
Responsibilities: -Individual LCMSMS handling. -Responsible for all type of Bioanalytical documentation. -Method Development, Validation and Study sample analysis. -Responsible for Operation, Cali
Production : • Supervision of production & maintenance activities of respective shift. • To ensure that every raw material used is of right quality (approved from QC, having reference Number) and qu
"Principal task : Lab demonstration & scale up of new DMF and NDMF molecules, Process Optimization before Scale-up activities, Execution of lab experiment & technology transfer activity. Responsibi
Principal task and Responsibilities: -Supervising & performing production activities of Streptokinase Drug Substance, Erythropoietin Drug Substance, Anticoagulant Drug Substance and Drug product, GCS
• To maintain and adherence of the GLP and safety procedures in laboratory. • To perform the analysis as per work allocation and records the results in work sheet (Protocols) for raw material / packi
Principal task and responsibilities : • To verify raw material/ packing materials as per BPR/documents at work place with coordination of warehouse. • To coordinate with engineering departments for
Lead and manage site-wide QMS activities, including deviations, CAPA, change control, risk management, investigations, complaints, and annual product quality reviews (APQR/PQR). Ensure implementation
• To maintain and adherence of the GLP and safety procedures in laboratory. • To perform the analysis as per work allocation and records the results in work sheet (Protocols) for raw material / packi
Major Purpose Of The Job:- To follow cGMP as per training guidelines from the premises to their section. To follow the respective equipment SOP’s and written procedure from BMR To ensure environm
Production : • To check the labels of raw material, packing materials and solvents before usage. • To maintain storage conditions of raw material/intermediates in plant. • To maintain process condi
Company: Novo Nordisk Global Business Services (GBS) Shape the safety narrative behind medicines that reach millions of patients worldwide. In this role, your words don't just inform — they protect. Y
Department: AI Reinvent & Engineering, Enterprise AI Company: Novo Nordisk Global Business Services (GBS) Bengaluru, India Are you excited about using AI to improve patients' lives? Do you thrive on c
Department: AI Reinvent & Engineering, Enterprise AI Company: Novo Nordisk Global Business Services (GBS),Bengaluru, India Are you passionate about applying AI to improve patients' lives? Do you enjoy
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