Apprentice
• 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
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• 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
"• To plan daily Capsule filling activity per norms of cGMP. • To carryout cleaning and capsule filling activity as per requirement in Cephalosporin block. • To carry out in process checks during ca
Objective: To support the development, characterization and optimization of solid forms of APIs, intermediates or advanced materials. To conduct solid-form screening, crystallization studies, analytic
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
Principal task: 1) Analytical method development and validation, method transfer. 2) Calibration of analytical instrument system. 3) To maintain and observe GLP/GDP in working environment. Respons
"• To operate the CVC Bulk packing machine as per the norms of cGMP • To supervise the machine activity as per the standard output with GMP requirements • To carryout in process checks during packin
"• To operate the CVC Bulk packing machine as per the norms of cGMP • To supervise the machine activity as per the standard output with GMP requirements • To carryout in process checks during packin
"• Cleaning and operation of Coding and data matrix Coding Machine. • Cleaning and operation of Coding Machine. • Clearance of coding area and machine. • Preventive maintenance of coding machine.
•Preparation of Artworks for various components for Domestic, ROW, EU and USA markets. •Hands on various software i.e. Adobe Illustrator, Coral draw, Photoshop, InDesign. •Preparation of Cutter guide
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
To assure Quality and cGMP compliance of the products being manufactured and Packed for Cephalosporin Block. • To review MMD-I / BPR and release of the batches for further processing stage like Granu
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