Executive
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
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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
• Planning and Execution of all MMD-I & BPR preparation activity pertaining to Main Pharma Block, Cephalosporin Block, Penicillin Block & Rifampicin Block of Dholka, as well as Contract Manufacturing
Principal Task: 1) Routine analysis for GC-MS; ICP-MS; HPLC; DSC; TGA; PSD; XRD 2) Maintaining cGLP environment in laboratory. 3) Perform development; validation; calibration and release related ac
• 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
• 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 BPR • To ensure env
1. To develop Stable & Bioequivalent for solid oral products for Europe, ROW & Domestic Markets. 2. Technology transfer of developed products to plant level, this includes all TTD-related works. 3.
Maintain GLP in the laboratory as per regulatory requirement. Analytical method development as per ICH Guidelines. To perform In-process, routine and stability sample analysis. Perform the analyti
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