Elizabeth Vultaggio
Global Quality Manager at SK GC Americas- Claim this Profile
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Bio
Credentials
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Certified IATF 16949 Supplier Auditor
AIAGMar, 2018- Oct, 2024 -
Six Sigma Green Belt
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Experience
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SK GC Americas
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United States
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Chemicals
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1 - 100 Employee
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Global Quality Manager
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Sep 2020 - Present
• Continued all the responsibilities and duties of the Business Quality Manager and added site specific operations responsibilities to ensure the continued certification and compliance to ISO 9001:2015• Scheduled, Coordinated, and prepared sites for external and internal audits• Collected, reported, and drove the improvement of global quality metrics • Drove the improvement of complaint management handling, reduction of times to cause, implementation of corrective action, and closure rates at a global level
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Business Quality Manager
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Apr 2020 - Sep 2020
• Drove the alignment, implementation and maintenance of the business quality programs and management system at a global level. • Represented the “Voice of Customer” for global sites.• Focal point for Product Stewardship and Regulatory needs within the Americas.• Lead cross functional teams to define the fundamental understanding of the organization’s critical process conditions with respect to the Quality Management System• Key interface to build and enhance relationships, services and flow of information between the global site and the customer, purchasing, supply chain, research, product stewardship and commercial organization related to the product quality, stewardship and regulatory requirements related to the quality management system.
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Quality Engineer
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Jan 2019 - Apr 2020
• Lead implementation and maintenance of the business quality programs and systems• Established auditing program, trained new auditors, and lead internal audit and process audits• Lead root cause investigations to drive resolution of customer product quality complaints• Lead quality and related management system plant training• Identified and lead improvement opportunities • Lead implementation and maintenance of the business quality programs and systems• Established auditing program, trained new auditors, and lead internal audit and process audits• Lead root cause investigations to drive resolution of customer product quality complaints• Lead quality and related management system plant training• Identified and lead improvement opportunities
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Oetiker Group
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Switzerland
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Motor Vehicle Manufacturing
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500 - 600 Employee
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Quality Engineer
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Sep 2017 - Jan 2019
• Lead & Manage Health & Safety team agenda, activities, investigations, and audits• Lead Internal auditor for internal audit team• Document Control Manager for Marlette’s local procedures and work instructions• Primary contact for customer quality complaints• Drive resolution of 8D’s and corrective actions throughout the organization• Provide support for PPAP & new product and process validation activities • Lead & Manage Health & Safety team agenda, activities, investigations, and audits• Lead Internal auditor for internal audit team• Document Control Manager for Marlette’s local procedures and work instructions• Primary contact for customer quality complaints• Drive resolution of 8D’s and corrective actions throughout the organization• Provide support for PPAP & new product and process validation activities
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Legal Intern
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Feb 2017 - Sep 2017
• Research federal law applications and locate avenues for clients to reduce or avoid prison and substantial fines• Draft legal documents and papers to negotiate terms and argue legal standing with the prosecutor• Meet with clients • Research federal law applications and locate avenues for clients to reduce or avoid prison and substantial fines• Draft legal documents and papers to negotiate terms and argue legal standing with the prosecutor• Meet with clients
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MB Aerospace
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United Kingdom
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Aviation and Aerospace Component Manufacturing
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300 - 400 Employee
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Quality Manager
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May 2016 - Oct 2016
• Managed the Quality Supervisor, Quality Engineers, CMM Programmers, NDT level 3’s, Calibration department, and PPAP Administrator• Implemented an aggressive Internal Audit Program• Resolved Customer complaints & Non-conformances• Quality Management representative in NADCAP audits, AS 9100 audit, and Customer audits• Maintained relationships with key suppliers to quickly resolve quality shortfalls• Restructured multiple QMS procedures to better align with quality standards and to improve compliance• Interfaced with other managers & departments regarding current and planned quality initiatives• Ensured all PPAP submissions were accurate, complete, and submitted to customers on schedule
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Cameron, a Schlumberger company
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United States
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Oil and Gas
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700 & Above Employee
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Quality Engineer
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Dec 2012 - May 2016
Regional Quality Engineer in the Rocky Mountains for Cameron's surface division• The face of Quality for 10 Cameron Surface facilities.• Manage the implementation and compliance to the Quality Management System for 10 Cameron Surface facilities• Supervise and train inspectors on performance requirements to SP, QP, and other BOM requirements as they relate to repair and inspection of equipment• Handle testing & certification of inspectors• Assist facilities in compliance to API Q2 and ISO requirements• Create new facility manual procedures, facility work instructions, and facility quality forms• Provide extensive support, e.g. root cause analysis and investigation activities for all my facilities to address & complete Corrective and Preventive Actions, Non conformances, and Field Performance Reports• Perform annual management reviews • Lead auditor on internal audits • Lead auditor on vendor audits to add Machine Shops and NDT vendors to Cameron’s Approved Vendor List• Set up vendors in SAP for Cameron’s Approved Vendor List• Participate in Customer Audits and third party audits as required• Train and educate facilities on SAP • Perform QIRs, correct QM lot errors, Modify Material Master Quality Inspection &procurement keys
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Milestone AV Technologies
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United States
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Appliances, Electrical, and Electronics Manufacturing
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1 - 100 Employee
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Quality Engineer
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Apr 2007 - Nov 2012
Quality Engineer• Trained employees during Business System Transition to SAP in both domestic and foreign offices & continued to support SAP through the creation of work instructions and testing of SAP applications• Subject matter expert for SAP Receiving Inspection activities (e.g. set up & management)• Created the Corrective and Preventive Action (CAPA) procedure& trained the organization • Lead and drove inter department CAPAs in both the US and China offices• Responsible for identifying & resolving quality issues with both foreign and domestic suppliers• Collaborated with manufacture engineers, quality representatives, and management teams to create and improve existing process controls for the manufacture of Milestone products• Coordinated with the University of St. Thomas for Six Sigma Green Belt training at Milestone • Audited the process controls of Chinese vendors • Active in Supplier selection and first article inspections• Analyzed and reported technical data to upper management for CAPAs & process capabilities
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Boston Scientific
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United States
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Medical Equipment Manufacturing
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700 & Above Employee
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Quality Engineer
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Sep 2004 - Feb 2007
Quality Engineer• Sole cross shift quality engineer providing extended onsite support for 2 manufacturing floors and a drug mixing room.• Lead process improvements & successfully drove numerous cross department CAPAs utilizing numerous six sigma tools, risk analysis, process monitoring, and trending analysis • Actively lead and organized cross department investigations into critical field complaints. • Mentored and trained engineers new to the organization and/or quality engineering on CAPAs and also on the mixing of the Taxus® drug component.• Participated in FDA audits• Participated in submission to Japan for releasing Boston Scientific products in the Japanese market
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Education
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2006 - 2010
Hamline University School of Law
Doctor of Law (JD) -
1998 - 2003
Michigan State University
Bachelor's degree, Biosystems Engineering
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