Leadership Effectiveness Training (L.E.T.) Webinar

Leader Effectiveness Training (L.E.T.) is a workshop designed to help participants learn the principles and skills needed to increase their effectiveness in their leadership roles. L.E.T. places a very heavy emphasis upon skill practice and mastery. The basic learning model includes presentation of a concept, discussion, demonstration, practice, feedback and discussion/application. This sequence is followed […]

APQP 3rd Edition and Control Plan 1st Edition Overview

Advanced Product Quality Planning (APQP) is a structured stage-gate process for new product development used by many companies from the automotive sector. In the last few years, the APQP process has been adopted by many industry segments, including the Aerospace/Defense, Medical and other industries. APQP extends beyond new product development, involving cross-functional collaboration from understanding […]

Embrace the Power of ISO 27001

In today’s digital age, information is a prized asset for businesses. As cyber threats evolve in frequency and sophistication, safeguarding sensitive data has become paramount. Enter ISO 27001 – a beacon of assurance and guidance in the realm of information security. ISO 27001 isn’t just compliance regulations; it’s a comprehensive framework by the International Organization […]

Introduction to ISO 13485

This one hour session will give employees an introduction to using, implementing ISO 13485:2016 and the GMP requirements for use in the Medical Device Industry. We will review what are some of the current requirements, some of the necessary training that employees should have and how to use ISO 13485:2016 and the GMP requirements to […]

Where do 7 Wastes (TIMWOOD) fit in the Toyota Trilogy of Wastes (Muda, Mura, & Mira)?

In the early 1950s, Eiji Toyoda and Taichi Ohno of the Toyota Motor Corporation visited the Ford River Rouge Complex in Dearborn, Michigan. They subsequently defined three different types of waste – Muda (waste), Mura (unevenness), and Muri (overburden) – that impact the flow of products and services and upon their return to Japan waste […]

So, How Will You Audit a Risk Assessment?

A sound approach to quality risk management utilizes the knowledge and experience of the entire team in your organization. The Team includes the people participating in the risk assessment, the people executing the mitigations as well as the internal auditors who need to evaluate the effectiveness of the process. Everyone needs to work together to […]

Principles of Lean Office

In the beginning of a Lean journey, the tools and concepts are typically applied on the factory floor. Since administrative inefficiencies can be more difficult to see than those in the manufacturing process and bottlenecks are not as obvious as they are on the shop floor. Too often, organizations ignore the waste and delays built […]

ISO 13485 and QSR Effective Implementation

In this seminar we will outline steps needed to meet the ISO 13485:2016 and QSR requirements for the medical industry and what changes are on the horizon. The ISO 13485:2016 requires numerous additional requirements to ISO 9001 that can impact a companies QMS. The seminar is geared to helping employees understand what is needed.

How to Increase the VALUE of Your Supplier Auditing Program

In a world of ever-increasing costs and price pressures from customers, companies are focusing on cost-control and streamlining efficiencies more than ever. Supply chains are continuing to expand, making it increasingly difficult and expensive for companies to effectively manage their supplier base. In addition, companies are being held to higher accountability for quality of product […]

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