Steve Obolewicz

Senior Consultant and Laead Auditor at SAI Global Limited

Location:
680 George St, Sydney, New South Wales, Australia
Company:
SAI Global Limited
HQ Phone:
+61 2 8206 6010
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Last Updated 12/5/2016

General Information

Employment History

Certified Quality Systems Lead Auditor  - RAB

Education

BS  - Physics , University of New York

MBA  - Marist College

Affiliations

Member  - Project Management Institute , Inc.

Member  - ASQ

Member  - Institute for Environmental Sciences

Web References  

Steve Obolewicz

Steve Obolewicz Steve ObolewiczBackgroundSteve Obolewicz has over 30 years of in-depth experience within the military/ aerospace, automotive, consumer electronics, medical device and pharmaceutical industries in the areas of Quality/regulatory Management (FDA GMP/QSR and 21CFR820), Reliability Engineering, ISO 9000/QS-9000/TL 9000 Quality Systems, Quality Assurance, Total Quality Management and Malcolm Baldrige National Quality Award criteria. Prior to joining SAI Global, Steve worked as a Quality Officer for a Fortune 100 company, prior to that he was Director of Program Management responsible for product development process, and also a Quality/Reliability Engineer and Manager for military, government and aerospace industries.He was also a Quality/Regulatory Specialist for a Medical Device and Diagnostics (IVD) company. Steve led one of the first companies in the US to ISO 9001 registration, and he has been instrumental in developing and implementing total quality management initiatives in several major companies. SpecialtiesOne of Steve's strengths is his ability to link design engineering practices to manufacturing.He has implemented these links in both hardware and software development environments, helping to streamline the introduction of new products.In this role, Steve has provided customers with the direction how to integrate ISO 9001 or ISO13485 into business processes to create value and integrity. Further, for our Medical Device manufacturing customers, he has advocated the proper use of FDA QSR per the Safe Medical Device Act.Lately, he has assisted several Medical Device companies with Risk Management in accordance with ISO 14971:2000 Also, Steve is a subject matter expert (SME) in TL 9000.He is a participant in the QuEST Forum teams (since 1998) for both TL 9000 handbooks, is an active member on sub-teams, and has been the key developer of the QuEST Forum sanctioned TL 9000 training courses.He has trained registrars, telecom service providers, and suppliers, as well as providing consulting services for some of the industries top suppliers. ClientsAs a Senior Consultant with SAI Global and as a former tutor for the BSI Lead Auditor course, Steve has trained more than 4,000 people.Steve received his BS in Physics from the University of New York in New Paltz, NY and his MBA from Marist College in Poughkeepsie, NY.Steve is a member of the ASQ.In addition, he is a member of the Project Management Institute (PMI), and the Institute for Environmental Sciences (IES).He is also an RAB Certified Quality Systems Lead Auditor since 1993.

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Steve Obolewicz

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Steve Obolewicz
Steve Obolewicz Background Steve Obolewicz has over 30 years of in-depth experience within the military/ aerospace, automotive, consumer electronics, medical device and pharmaceutical industries in the areas of Quality/regulatory Management (FDA GMP/QSR and 21CFR820), Reliability Engineering, ISO 9000/QS-9000/TL 9000 Quality Systems, Quality Assurance, Total Quality Management and Malcolm Baldrige National Quality Award criteria. Prior to joining SAI Global, Steve worked as a Quality Officer for a Fortune 100 company, prior to that he was Director of Program Management responsible for product development process, and also a Quality/Reliability Engineer and Manager for military, government and aerospace industries. He was also a Quality/Regulatory Specialist for a Medical Device and Diagnostics (IVD) company. Steve led one of the first companies in the US to ISO 9001 registration, and he has been instrumental in developing and implementing total quality management initiatives in several major companies. Specialties One of Steve's strengths is his ability to link design engineering practices to manufacturing. He has implemented these links in both hardware and software development environments, helping to streamline the introduction of new products. In this role, Steve has provided customers with the direction how to integrate ISO 9001 or ISO13485 into business processes to create value and integrity. Further, for our Medical Device manufacturing customers, he has advocated the proper use of FDA QSR per the Safe Medical Device Act. Lately, he has assisted several Medical Device companies with Risk Management in accordance with ISO 14971:2000 Also, Steve is a subject matter expert (SME) in TL 9000. He is a participant in the QuEST Forum teams (since 1998) for both TL 9000 handbooks, is an active member on sub-teams, and has been the key developer of the QuEST Forum sanctioned TL 9000 training courses. He has trained registrars, telecom service providers, and suppliers, as well as providing consulting services for some of the industries top suppliers. Clients As a Senior Consultant with SAI Global and as a former tutor for the BSI Lead Auditor course, Steve has trained more than 4,000 people. Steve received his BS in Physics from the University of New York in New Paltz, NY and his MBA from Marist College in Poughkeepsie, NY. Steve is a member of the ASQ. In addition, he is a member of the Project Management Institute (PMI), and the Institute for Environmental Sciences (IES). He is also an RAB Certified Quality Systems Lead Auditor since 1993.

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