Operator
• 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 environmental condition of Gran
Find Pharma, Biotech, Clinical Research & Medical Jobs on Bioksha
• 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 environmental condition of Gran
"• To ensure smooth and efficient functioning of plant machineries at main Pharma block. • To attend routine breakdown maintenance of production machinery of main pharma block. • To attend the modi
Production : • Cleanliness of the equipments and area under his charge. • Operations of Reactors, Centrifuge and other equipments like vacuum pumps, Filter units, scrubbers, dryer, blender, shifte
Principal task and Responsibilities: -Supervising & performing production activities of Streptokinase Drug Substance -Troubleshoot the technical issues in consultation with the Production Head durin
Major Purpose of the Job: - • To ensure that cGMP practices shall be followed from the premises to their section. • To follow the all respective SOPs & BMR procedure in the department during operati
• 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
Production : • Cleanliness of the equipments and area under his charge. • Operations of Reactors, Centrifuge and other equipments like vacuum pumps, Filter units, scrubbers, dryer, blender, shifte
Process Development: • Conduct laboratory experiments & trials to modify processes develop shorter processes to reduce present cost. • Send sample to QC of studied experiment. • Contact QC dept. to
Compression Operator Responsible to take care of cleaning of area, cGMP, GDP, Productivity of machine etc
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
• 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 environmental condition of Gran
Production : • Cleanliness of the equipments and area under his charge. • Operations of Reactors, Centrifuge and other equipments like vacuum pumps, Filter units, scrubbers, dryer, blender, shifte
• Ensure the c-GMP Compliance and schedule M compliance in production. • Ensure the completion of production targets with zero quality issue. • Ensure the compliance of inspection /Audit in coating
• Compliance to cGMP and other regulatory requirement. • To monitor the daily packing activates in Secondary packing in with compliance of cGMP norms. • To execute packing inputs as per shift plan i
1) Planning of analytical activity for assign Projects. 2) Review of Routine (F & D) and stability sample analysis as assign Projects and compilation. 3) Review of Specifications and Standard Test
Monitor and track project activities from inception to closing. Proactively interact with managers within the organization during the course of the project. Working towards increasing the project mana
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
• Execution of plans for cell culture group • Preparation of media for cell culture purpose • Preparation of buffers • Cell Line maintenance • Calibration of pH meter • Handling and knowledge of
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 en
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