Operate manufacturing equipment according to SOP`s ,cGMP`s,or FDA guidelines Filling,Dispensing,Compounding & PackagingPerform simple,routine,complex,& critical operationsEnsure process equipment is appropriately maintained for operationExcute validation & equipment qualification protocolsRoutinely draft & revise standard operating procedures and master batch recordsRecognize and initiate process deviation reviewsTroubleshoot equipment issues,when necessaryConduct daily activities in an organized, efficient mannerSupport continuous improvement initiatives by identifying areas needing improvement,recommending strategies for improvement,& implementing those strategies once approvedMaintain training compliance & ensure a safe working environment for all the staff.Performed a weekly, monthly, or semi-annual cleaning after each batch run according to SOP`s Stock the gowning area on a daily basis with supplies gowns, booties, hairnets, beard coverings & glovesInventory check to ensure supplies was available for restock etc...,

o Operate Dispensing ,Componding ,Filling EquipmentOperate Klurring, ACM, DFP ,Smart Scope, and Packaging Equipment on a rotating basis o Monitor and audit work processes to ensure compliance and completion of targetso Sample product for release testing & special jobs require Water Bath testingo Clean and maintain all equipmento Dispense raw materials & components for manufactureCollecting samples for in-process testing and complete test and inspection activitieso Conduct preventative maintenance activities, where appropriate and monitored HMI and POC control systemso Assist in maintaining equipment records pertaining to PM and calibration activities, and equipment warrantiesPerform good documentation of processes; maintain and prepare production documentation; maintain good documentation on Master Batch Record, Electronic Batch Record and logbooks• Communicate production issues to Manufacturing management to improve manufacturing operations.• Assist in creating and revising SOPs, investigations, and all forms of cGMP documentation• Document production activities per Pearl SOPs, cGMP ,& OSHA policies and procedures.• Maintain the inventory of consumables and supplies required for GMP production.• Participate in staff meetings and special project teams where required• Maintain a safe working environmento Observe and follow all safe GMP`S operation practiceso Routinely inspect facility safety equipmento Maintain in a Cleanroom & clutter free production environment Perform daily biomanufacturing operations under strict adherence to cGMP, OSHA, and AstraZeneca policies and regulations

⦁ Assembled, fit and mount sub-assemblies, components, and standard assemblies in electrical control equipment. ⦁ Assembled & wire units, relay panels, panel boards, space heaters, and control panels. ⦁ Bend and install power cable and MTB harnesses & power leads. ⦁ Used established power checking procedure(s)to test according to Schematic - Blue Print to verify electrical or mechanical integrity of units assembled.⦁ Installs,troubleshoots,repairs & calibrate low voltage AC/DC electrical and instrumentation.⦁ Interfaces with OEM`s & Vendors as necessary .⦁ Requisitions equipment as needed .⦁ Performs repairs & modifications as directed by maintenances supervisor / plant management.⦁ Supports or leads failure analysis process by discussing the causes for equipment failure with maintenance/ engineer.⦁ Accurately completes all requried paperwork,forms,calibration reports (ICIR) & PM checklists .⦁ Assist in staging department to perform inventory cycle count of parts in stock and need to be ordered .