Apprentice
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
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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
Major Purpose Of The Job:- • To review Daily Packing plan for the assigned Packing line activities. • To ensure that arrangement of dispensed batches for the day in advance. • To ensure that Daily
To perform In-process Quality Assurance for the process / products being manufactured and packed in Main Pharma Block (Tablet / Capsule). To ensure Quality and cGMP compliance of the products being m
• Review of analytical data of scale up and validation batches, commercial batches of finished products and also of raw materials, packing material, in process, intermediate, hold time study, stabili
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
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 ensure Registration dossier submission of products in different SEA countries (Region II), Africa countries (Region I) as per agreed timeline. To ensure Renewal of registered product prior to va
On line documentation in BMR ,BPR ,Annexure & Log book on daily basis as per GMP requirement . Change Over , Cleaning & Operation of Bottle Washing machine as per production plan . Change & over ope
To perform the in process checks for control on production for the process / product being manufactured. To ensure Quality and cGMP compliance of the products being manufactured. Parenteral Manufact
"• Operation, & Maintenance, of all packaging equipment & Parenteral of following block: Main Pharma Block. Cephalosporin Block, Rifampicin Block • Operation & Maintenance of associated systems •
• To maintain and adherence of the GLP and safety procedures in laboratory. • To issuance of work data sheet / protocols from Q.A Department. • To work as Analyst and maintain the CFR 21 part -11 co
• Align production capacity with sales forecast and market demand. • Develop 12–36 month demand and supply plans for pharmaceutical products. • Evaluate manufacturing capacity, resource constraints,
• Perform financial analysis of supply chain operations including procurement, manufacturing, logistics, and inventory. • Prepare monthly variance analysis against budgets and forecasts. • Develop f
Major Purpose of the Job • Analysis and documentation of finished Goods. Principal Tasks: • To analyse finished goods, semi-finish and In-process samples. • Analytical result recording in LIMS a
Principal Tasks: • To analyse finished goods, semi-finish and In-process samples. • Analytical result recording in LIMS and SAP. • Specification, Master, Record of Analysis preparation/correction i
• Lead and manage the end-to-end P2P cycle including requisition, sourcing support, PO creation, goods receipt coordination, and invoice reconciliation. • Ensure procurement transactions comply with
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 BPR • To ensure env
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 quanti
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
"• Responsible manufacturing activity of Liquid Bulk, • Filling Machine, Bottle washing machine change over, & operation as per schedule. • Responsible for change over & operation of Labeling, Aut
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