Updated to the latest standard changes including ISO 9001:2015, ISO 14001:2015, and ISO 45001.
Includes guidance on integrating Corporate Responsibility and Sustainability.
Organizations today are implementing stand-alone systems for their Quality Management Systems (ISO 9001, ISO/TS 16949, or AS9100), Environmental Management System (ISO 14001), Occupational Health & Safety (ISO 18001), and Food Safety Management Systems (FSSC 22000). Stand-alone systems refer to the use of isolated document management structures resulting in the duplication of processes within one site for each of the management standards-QMS, EMS, OHSAS, and FSMS. In other words, the stand-alone systems duplicate training processes, document control, and internal audit processes for each standard within the company. While the confusion and lack of efficiency resulting from this decision may not be readily apparent to the uninitiated, this book will show the reader that there is a tremendous loss of value associated with stand-alone management systems within an organization.
This book expands the understanding of an integrated management system (IMS) globally. It not only saves money, but more importantly it contributes to the maintenance and efficiency of business processes and conformance standards such as ISO 9001, AS9100, ISO/TS 16949, ISO 14001, OHSAS 18001 / ISO 45001, FSSC 22000, or other GFSI
Standards.
Giới thiệu về tác giả
R. Dan Reid, the Omnex Director of Consulting, is best known as an author of QS-9000, ISO Technical Specification (TS) 16949, ISO 9001:2000, the first ISO International Workshop Agreement (IWA 1), which applies ISO 9001 to healthcare and its replacement, AIAG’s Business Operating Systems for Healthcare Organizations (HF-2). He also worked on the Chrysler, Ford, and GM Potential Failure Mode and Effects Analysis, Production Part Approval Process, and Advanced Product Quality Planning manuals.
While at AIAG, Dan led successful projects for Effective Problem Solving, Cost of Poor Quality, and Supplier Management. While at General Motors, among other assignments, he led the Supplier Development Administration, served on the Chrysler, Ford, GM Supplier Quality Requirements Task Force, which was responsible for QS-9000 and later ISO/TS 16949, and he established a Supplier Quality function at GM Service Parts. He later established a Supplier Quality function at Baxter Bio Science Division’s Los Angeles plant before serving as the Bio Science Divisional Supplier Quality Director.
Dan, an ASQ Fellow and ASQ Certified Quality Engineer (CQE), has received numerous awards and is recognized for a number of accomplishments:
• The first Delegation Leader of the International Automotive Task Force (IATF)
• A member of the Parenteral Drug Association
• A member of the American College of Health Care Executives
• A published author with Mc Graw Hill, ASQ Quality Press, and others
• A member of the ASQ Administrative Committee and Technical Reviewer
• On the A2LA Board of Directors
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