Technical Supervisor
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
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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
• To prepare Technical Comparison & forward to purchase for recommendation • Coordination with consultants for planning & designing. • To ensure the raising of indents in SAP as per design in elect
• To ensure civil maintenance work of all the plant. • To ensure strict compliance of cGMP requirement & good engineering practice requirement besides other statutory laws, rules and regulatory comp
• Develop and implement sourcing strategies for APIs, excipients, packaging materials, and indirect procurement categories. • Identify, evaluate, and onboard new suppliers in alignment with quality a
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
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 maintain and adherence of the GLP and safety procedures in laboratory. • To raise the request for issuance of work data sheet / protocols. • To work as Analyst and maintain the CFR 21 part -11
Principal task and Responsibilities: •Provide strategic leadership across all R&D verticals: Synthetic Labs, ADL, PERL. Process Development (Plant), and Tech Transfer. • Drive new product developme
• 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 : • 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
• 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
• Perform financial analysis of supply chain operations including procurement, manufacturing, logistics, and inventory. • Prepare monthly variance analysis against budgets and forecasts. • Develop f
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
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 • Analysis and documentation of finished Goods. Principal Tasks: • To analyse finished goods, semi-finish and In-process samples. • Analytical result recording in LIMS a
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
• 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
• 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: -Formulation development of oral solid and liquid oral products for regulated, semi regulated and other international market. - Technology transfer, Process and Cost opt
"• 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
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