The risk of fraud is very real and unfortunately, happens often. Fraudulent activities have always been woven within the corporate fabric and cuts across industries, businesses and governmental establishments. History has shown that the impact of fraud can be catastrophic and have a lasting adverse effect. Fraud events have increased in recent years due to a variety of reasons including the financial benefit, opportunity, motive, justification or rationalization. Certainly, its awareness, prevention and early detection are very important in sustaining a quality management system. The discussion will include:
- Lessons Learned: Con Edison’s fight against fraud.
- The common areas of fraud risk and the key red flags to look for.
- A discussion of factors that create a perfect environment for fraud to thrive.
- An understanding of the components of quality management and how fraud hinders its achievement.
- Resourceful ways of combating fraud.
Continue reading Section Meeting: A Clog in the Wheel of Quality Management
Please join us for our April 2018 Section meeting where Corie LaRocco will lead an introduction to Quality in Aerospace Manufacturing. During the guided discussion we will explore various topics including:
- Company Quality Requirements for doing business
- Documentation & Flowdown
- Mfg – Working within standard requirements
- Special processes & certification
- Product approval
- Corrective / Preventative Action
- Continuous Improvement
Continue reading Program: Intro to Quality in Aerospace Manufacturing
This event is a General Section Meeting where attendees are invited to bring a spouse or significant other. The February 2018 Section Meeting and Singapore Culture Presentation will be preceded by an optional tour of Grand Central Terminal. A Tour Guide will lead a 75 minute tour of historic Grand Central Terminal, currently the home of Metro-North Railroad and soon to be a second Manhattan destination for the Long Island Railroad in addition to its current Penn Station destination. Tour Guide will lead the tour group through the Terminal describing its grand history and current operations. Following the tour, the group will walk to nearby Annie Moore’s Bar and Restaurant for the Section Meeting, including dinner and a very informative presentation on Singapore Culture and Quality.
Time & Place:
- Tour: 4:00-6:00pm, Grand Central Terminal Main Concourse at the Information Booth under the Historic Clock
- Section Meeting: 6:30-8:30 pm, Annie Moore’s Bar & Restaurant, 22 East 41st Street, New York, NY 10017 Phone: 212-986-7826
All attendees (members, non-members, spouses/significant others must register through Eventbrite. Please note for this event each attendee must have separate tickets for the tour and the Section Meeting/Presentation)
Continue reading Section Meeting: Singapore Culture and Quality Presentation and Grand Central Terminal Tour
Many of us work in a regulated environment. We may work on the manufacturing floor of a pharmaceutical company or we may work in a clinical laboratory in a hospital. Many of us may work in a government laboratory or in an academic laboratory in a university. There is a common thread impacting all these settings which is known as cGXP. cGXP is a set of regulations which impact an organization to stay within compliance so as not to harm the public and result in closure of the institution. Within cGXP there are three categories which impact most workplaces and they are; cGMP, cGCP and cGLP. I will explain how these categories differ and the consequences that occur by not following these regulations. I am hoping that after this presentation, if you see something that is incorrect at your work place you will be able to cleverly point it out to your QA/compliance manager.
Whether it is in the laboratory, manufacturing floor or in the clinic there are regulatory requirements to be met. cGXP for the most part are the guiding regulations and there is confusion how these regulations differ. Please attend this meeting to find out.
Continue reading Section Meeting: What Does cGXP Mean And What Are The Differences Between cGLP, CGMP and cGCP?
In 2015, ISO 9001 was not the only management system standard revised to include risk and opportunities requirements. The latest revision of ISO 14001 also now includes risk and opportunity requirements for an environmental management system (EMS). But how can your EMS meet these requirements? Join us for a presentation of one company’s efforts to incorporate risk in the EMS. Specific discussion points include: developing and managing an EMS risk assessment process as part of a larger risk portfolio, risk tools and techniques adopted for determining environmental aspect significance, developing tools to include sustainability efforts in the EMS risk assessment process, and developing tools to communicate EMS risk assessment results to stakeholders.
PRESENTED BY: Carl Johansen BSIT, MSTM, GRCP, GRCA, ISO 9001:2015 and ISO 14001:2015 Lead Auditor Certified, Section Manager Utility Shared Services Quality Management, Con Edison
In his current role at Con Edison Carl is the Section Manager for the Utility Shared Services Quality Management department and the program manager for the company-wide certification of its environmental management system to ISO 14001. Carl is applying quality management techniques honed in the manufacturing industry to the energy and utility sector at Con Edison. In his spare time, Carl is an automotive enthusiast who enjoys MINI Cooper rallies and shows with friends.
Carl is an active member of ASQ holding the marketing chair for the Design and Construction Division (DCD), the technology chair for the Customer-Supplier Division (CSD), and he’s a member of the environmental management sub-committee of ASQ’s Energy & Environment Division (EED) in the role of environmental management SME.
Continue reading Section Meeting: Got Risk? Risk Assessment Tools for ISO 14001: 2015
September 19th – Healthcare: Value based Payment Model @ the Spanish Tavern in Newark