Qualifications:

• Advanced knowledge of and experience in merology, CMM operationand MCC manager software program bad Qcalc program
• Ability to manage, delegate, facilitate and train others.
• Excellent communications and organizational skills.

Responsibility:

• Develop PPAP (Production Part Approval Process) documentation for submission to customer for customer approval.
• Maintain appropriate module(s) in the database, in order to develop and or update as appropriate the changing needs of the customer,
• Maintain master samples of the approval PPAP (one part from each cavity)
• Develop and maintain a matrix identifying all special characteristics as referenced on the customer.
• Engineering drawings to include measurement methods.
• Champion and maintain the Gage calibration program.
• Conduct MSAa (Measurement System Analysis) Studies on all measurements methods used to verify special characteristics
• Notify management immediately if measuring methods become non-capable or unstable for immediate corrective action.
• Initiate Gage RandR studies (repeatability and Reproducibility) on gauging methods of special characteristics for PPAP.
• Maintain work area in a clean, neat and orderly manner
• Have understanding of root cause analysis and corrective actions process
• Effectively complete internal audit corrective action request in a timely manner.
• Ensure that the Quality Management Systems (QMS) is maintained in area of responsibility
• Conduct layered and process audits as scheduled
• Perform dimensional layout on components as directed by the Quality Manager.
• Shall be knowledgeable of and utilized advanced statistical concepts, such as variation control (stability)
• Process capability and over-adjustment when conducting analysis
• Track the status of the suspect product and distribute report to the Quality Manager
• Open and champion a corrective action until closed.
• Have authority to stop production to correct quality problems.
• Generate approved quality alerts memos for customer issues and post at the appropriate workstation including work instructions as necessary
• Review all documents in IQMS as per auto generate reminders and schedule
• Ensure quality records maintained within the quality lab are filed correctly and are easily retrievable.
• Conduct analysis on returned products and report date to the Quality Manager as appropriate
• Assist with other projects as requested by the Quality Manager
• Have flexibility to perform other tasks as required by the Quality Manager.