Technical Supervisor
• To prepare and review the PQRs. • To compile the quality attributes & In-Process parameter in PQR as per current version of SOP. • To verify & review of Ingredient manufacture name (Vendor Name) &
Find Pharma, Biotech, Clinical Research & Medical Jobs on Bioksha
• To prepare and review the PQRs. • To compile the quality attributes & In-Process parameter in PQR as per current version of SOP. • To verify & review of Ingredient manufacture name (Vendor Name) &
• Receipt of Raw Material for main Pharma stores. • SAP data entries like GRN, Issuance, Transfer posting, reservations, SAP report generation etc. • To check the environmental parameters like Tempe
. Responsible for operating vial/bottle and ampoule washing, filling and capping machine and PFS filling Machine at Dholka premises. • Should have knowledge of Operating and maintenance of vial/bottle
•To review Registration and Re-Registration Dossiers before submission in all Aus / NZ countries. •To maintain Country-wise registered products status for all AUS/ NZ countries. •To co-ordinate wit
Responsibility Lab demonstration & scale up of new DMF and NDMF molecules, Process Optimization before Scale-up activities, Execution of Kilo Lab batches & technology transfer activity. Princ
• Ensure receipt and on-line documentation of the materials received as per SOP. • Ensure all the operating systems are maintained as per the SOP. • To receive the materials as per the amended appro
• Follow cGMP and GLP practices in Quality Control Lab. • To follow safety procedure in qc department. • To analyze the Sample of in process validation and finish product on instrument such HPLC, GC
• 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/Weekly/Monthly packing sche
• Follow cGMP and GLP practices in Quality Control Lab. • To perform the qualification of working standard. • To Maintain Inventory management for all chemicals, solvents and laboratory required i
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 : • 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
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 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
• To supervise the machine activity as per the standard output with GMP requirements • To carryout in process checks during packing machine activities • To arrange packing materials as per shift pla
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
• 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
1. Field Work & Sales Achievement • Promote company products to the doctors and pharmacists in line with divisional strategies and guidelines. • Achieve the assigned sales budget through effective p
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