Job Title: MES Analyst
MES Analyst performs diversified duties including but not limited to: implement product Bill of Materials (BOM) and manufacturing flow configurations in Manufacturing Execution System (MES), ensuring that incoming materials are released for production, and maintains documentation of department policies and procedures and ensures compliance with FDA and MDT Quality Systems. MES Analyst also assists in the investigating/reconciling Work Order (WO) and material discrepancies in MES and ERP systems. During quality issues, MES Analyst preforms data mining to identify suspect materials and coordinates with production to contain suspect materials by executing Formal Quality Holds in FACTORY works.
Configure product BOM and manufacturing flow in MES based on product specifications to support Hybrid, IC Test, Die Prep and APF Wafer Operations across entire MTC campus
Review production specifications and documentation to configure systems (MES, ERP, ChemTrace, LIMS, ESV) to support manufacturing. Work with engineers on equipment change (ECA), task management (MEST) and engineering data collection (MESDC) documents to setup equipment configurations, tasks and engineering data collection in FACTORY works.
Work with Planning and Finance to investigate and reconcile material or Work Order discrepancies between MES and ERP systems
Work with engineering and sourcing team on setting up off-site processing flow at ASE and UTAC. Reconcile die count discrepancies on wafers against wafer maps in DMAS
Work with Manufacturing Operations to correct tracking errors
Perform device data mining to create device lot list to support quality issue investigation. Work with engineering and Quality Assurance (QA) teams to identify suspect device lots and coordinate with Planning and Ops teams to isolate non-conforming product during containment and assist in opening/closing Formal Quality Holds
Update DHR based on Non-Conforming Report (NCR) to support non-conforming product disposition. Implement appropriate system corrective action as needed to address NCR.
Run various MES data extract as required to support engineering evaluation or process improvement projects.
Provide Device History Record (DHR) to support audit activities
Review manufacturing specifications and process documentation and ensures compliance with FDA regulations and MDT internal quality policies.
Working with Product Development team on system enhancements needed to support the introduction of new manufacturing processes/products.
Provide user training on MES system.
Associate s degree required with 3+ years of experience in a manufacturing role preferred.
Working knowledge of MES (FACTORY works) or other MES systems.
Knowledge of Enterprise Resource Planning (ERP) system such as JDE or SAP
Proficient in MS Excel. Experience with data mining tool like Spotfire.
Ability to meet deadlines, self-motivated and shows initiative.
Good communication skills, both written and oral. Ability to communicate to all levels and advocate a team concept.
Continuous improvement focus, concern for quality
High degree in attention to detail
Lean Manufacturing and Medical device experience preferred but not required
Physical Job Requirements
The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
The work environment is an office setting with occasional floor time. This setting is noisy and may require hearing protection. Smocks, hairnets, and if necessary, beard covers must be worn in designated manufacturing areas. Occasional overtime is required.
Regularly Stand; Walk; Talk or Hear; Lift up to 10lbs
Frequently, Use Hand to Finger, Handle or Feel; Reach with Hands and Arms; Lift up to 25lbs
Occasionally Sit; Climb or Balance; Stoop, Kneel, Crouch or Crawl; Lift up to 50 pounds