Philip Davis Email & Phone Number

Indiana, United States

Auburn Hills, Mi, Us

Position Summary:The position will be responsible for supporting all Quality Assurance activities in the Global Powertrain scope.The position will be in support of the Global Quality Director and includes issue follow-up, training, TI Automotive Directed initiatives such as S/R, QBIC, 6S and cleanliness.Responsibilities of Position:1. Provides at will support of all Powertrain Quality/Operations Personnel globally.2. Roll-out/training of TI Automotive Powertrain facilities worldwide to ensure global adherence to best practices.3. Spearhead specific initiatives as directed by the Global Quality Director.4. Support the prescreening of supplier candidates for technical and feasibility before sourcing meeting as required.5. Participates in global sourcing committee reviews as required by the Quality Director.6. Drives, where necessary, Top Focus and supplier scorecard improvement activities. Including follow up monitoring supplier’s effectiveness to established goal and objectives.7. Champions’ resolution of chronic customer quality issues when requested: identifies, prioritizes, charts occurrences/trends, implements and manages corrective action plans, reports on corrective actions/problem resolution.8. Lead workshops to develop and mentor plant quality staffs and other key plant personnel in problem resolution (PPS), controls plans, 6S, QBIC, and Cleanliness.9. Drives the mandated “zero defects expectations.10. Facilitate global change management as required in supporting supplier change request.11. Performs monthly Divisional quality reporting roll-up and analysis. Will follow-up with key individuals in each PT location on specific customer and supplier issues in order to drive closure of the problem.

Vaughan, Ontario, Ca

South Bend, In, Us

Auburn Hills, Michigan, Us

Quality Engineering

Us

Quality Assurance/Environmental Health and Safety Manager (2004-2009) Administrated Quality Management System company wide in accordance with ISO/TS 16949:2002. Establish, document, implement, maintain and continually improve the QMS system and reducing rejects.  Established 15 QMS process procedures which includes: manufacturing assembly department, internal audit, control plans, FMEA’s, product audit, corrective/preventative action, root cause analysis, management review, customer expectations (PPM), material control, supplier development, and performance, receiving, shipping, and document control. Administrated Environmental Management System ISO 14001:2004. Establish, document, implement, and continually improve the EMS system plant wide.  Achieving the Chairman's Award: Accuride Corporation zero OSHA recordable injury

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Customer Service/Production Control (2000-2004/ 2008-2009) Facilitated all customer orders from initial order through delivery.  Managed million dollar inventory levels plant wide. Consisting of 35 components for the assembly process. Served as liaison between sales staff and customer.  Resolved all customer questions and concerns in a timely manner.  Tracked all order customer deliveries with a 100% on time delivery rating Guided customers of new and/or alternative products. To streamline their ordering process to help reduce costs.  Scheduled assembly lines. Determine customer requirements and to meet customer deadlines. Maintaining a 100% on time delivery

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 Performed all aspects of Quality Engineering. Performed machine and process capability studies and analysis for any potential process improvement Performed Internal Quality Audits. Planned and conducted quality management process procedure internal audits reporting results and retained associated records..  Supervised gauge repeatability and reproducibility studies in compliance with AIAG. Q.S. 9000 process manuals. Organized gauge and guided personnel to conduct studies and report results and corrective actions as necessary.  Supervised Q.S. 9000 Document and Data Control, work instructions, operations and QMS procedures. Maintaining and updating quality management system procedures as required.

Us

Monitoring and measurement of the manufacturing process to specific measurement techniques, sampling plans, acceptance criteria and reaction plans when criteria was not in accordance to control plans and process flow diagrams.Performed machine and process capability studies to measure performance and analyze characteristics for any process improvements.Planned and conducted quality management system internal audits to ensure the QMS is effectively implemented and maintained. Documented results and retained associated records.Planned and supervised gauge repeatability and reproducibility (GR&R) studies in compliance with AIAG Q.S. 9000 Measurement System Analysis manual.Supervised Q.S. 9000 control documents. Approved documents for adequacy prior to issue, reviewing and updating, as necessary, to ensure correct revision levels for Control Plans, Work Instructions, and Level III documents.Performed inspection on incoming purchased material including dimensional inspection, destructive, tensile strength, Rockwell hardness and non-destructive Magnetic Particle (Magnaflux) testing.Trained new employees in blueprint reading, basic mathematics, and Statistical Process Control. Performed all Production Part Approval Process (PPAP) and controlled all elements requirements for supplier and customers PPAP package.Performed dimensional inspection on in-process product. Inspected product using all types of precision instruments, micrometers, calipers, height, dial indicators, and surface indictors.Managed company gauge calibration program. Calibrated all company and employee gauges traceable to NIST.Managed operator certification program training operator on how to read blueprint, in-process dimensional inspection, SPC, basic math, and document control.