Find Pharma, Biotech, Clinical Research & Medical Jobs on Bioksha
• 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.
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
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
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
• Build and maintain scenario planning models to assess supply chain risks and opportunities. • Analyze demand variability, supply disruptions, cost impacts, and capacity constraints. • Collaborate
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 •
Looking for something specific?
Browse all job categories →