Job description

Description oComplies with all PHMI Quality System procedures, Work Instructions and company Standard Operating Procedures (SOPs) oValidate developed process and recommend process improvement. oFamiliarize Production and QA personnel regarding assembly process for new products. oDevelop assembly processes on all areas of the Production for new products. oResponsible in generating assembly Process Flows and Work Instructions for assigned projects/product. oResponsible with the updating of Assembly Process Flows and Work Instructions based on released ECOs. PMD-JO, line balancing and process improvements. Coordinates with Project Manager for product changes oPrepares Qualification Report for new product and consumable materials. oCommunicates to the Lead Project Manager for the development of a new product. oWorks with PCD and Project Manager for the quotation of new and/or potential products. oConducts Failure Analysis on the top three rejects being encountered by production line. oConducts evaluations as may be assigned by the Project Manager. oResponsible in spearheading the generation and re-evaluation activity of HPRRs for medical device products. oConducts Plant Visit on suppliers that are for qualification upon providing sample parts of new products. oA time-to-time visit to PCBA sub-contractor/parts vendor while PCB assembly or fabrication is on-going. oResponsible for ensuring that all parts are complete on the production floor prior to commencement of the Pilot Run. oMakes suggestions for improvement to PHMI Quality system or operating procedures in constructive manner (when appropriate) oInvolves in the analysis or trouble-shooting of products for repair that are causing difficulty to repair technicians. oPerforms other related job as assigned. Requirements Minimum education level: Bachelor´s Degree Years of experience: 2 Language(s): English Knowledge: Engineering Availability for travel: No Availability for change of residence: No