IPQA Of Tablet Capsule SectionDaily QA Inspection Of Manufacturing. in Process CheckingProductionPacking Department. Pharma ProductionWalk in
Daily activity report. IPQA of Tablet and Capsule Section. In process checking , production and packing department. Daily QA Inspection of entire Manufacturing. Measured Values Obtained From the process equipment(ex:temperature, RPM etc.) Process attributes (ex: weight, hardness , friability etc.)
Microsoft Office Quality ControlHPLCQuality AnalysisFinished ProductsProduction ControlWalk in
Systematic planning and preparation of product labels, handling and distribution of product BOMs SOP and specification sheets.Process control to eliminate deviation in FGs.Knowledge of QMS principles / GMP requirements in a food industryKnowledge of shop floor activities and man managementShould have robust knowledge of FSSC 22000 & FSSAI regulationsKnowledge of analytical techniques and operation of basic instruments used in quality function of a food process industryPersonal Attributes:Able to communicate and motivate coherently (both written & verbally)Using problem solving skills and root cause analysis to resolve and/or mitigate operational issuesGood supervisory, planning & training skillsHigh level of integrity and character Ready to work in rotational shiftSelf-starter and able to anticipate work requirementsFlexible to change schedule and hours of work to meet the needs of the plantAbility to undertake and perform duties to a satisfactory level in a busy work environment
Chemical Engineer Chemical ProductionProduction ChemistChemical MaintenancePlanning ExecutiveProduction ExecutiveWalk in
Look overall Production & store activities independently. Daily Work Distribution planning and monitoring. Bulk & Finished Products intimation. All machinery cleaning & log- book R.H Manufacturing formulation development for product. IPQA presentation to management. Issuing of documents. Approval of Standard Operating Procedure & work Machinery. Review of all master formula sop & BMR/BPR. Raw materials stock maintained. Maintaining Current Goods Manufacturing Processes (c GMP W.H.O) at all stages of production. Review of production records. In process checks including area and line clearance at all stages from dispensing to dispatch. Maintained for finished goods. Quality audits Internal and External), vendor assessment
Planning Manager Manpower HandlingChemical EngineerChemical ProductionProduction ChemistChemical MaintenanceWalk in
Personal will be responsible for managing day to day affairs of production of the manufacturing setup , maintaining S.H.E , and achieving production targets. Personal will be responsible for a group of products.