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
We have officially launched our LinkedIn page for our ASQ NY/NJ Metro Section! Stay updated on our events and news through our page.
ASQ North Jersey Section is hosting a preparation course and workshop for Certified Quality Engineer (CQE) starting on January 6th, 2018
Please register before December 25th if you are interested. To register please send the completed registration form to Carl Perini at firstname.lastname@example.org
Location: Saint Paul’s Congregational Church, 10 St. Paul’s Place, Nutley, NJ
CERTIFIED QUALITY ENGINEER (CQE) – Public classes are held on consecutive Saturdays starting about 9 AM Course length: 40 hours
This course helps prepare the student for the Certified Quality Engineer examination. It offers a detailed review of the body of knowledge which is covered in this examination. The amount of material covered is extensive and students are expected to have a firm basic background in most areas of Quality Engineering.
Review the instructor’s profile on LinkedIn – Mike Parrillo – https://www.linkedin.com/in/parrilloasq
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
Infinite Consulting Corp (ICC), a program and construction management consulting firm, is in need of a full-time Quality Manager for a major New York City Transit station enhancement project.
The Quality Manager must possess the following qualifications:
• ISO 9000 or ASQ certified
• At least 5 years of experience
• Rail/transit experience preferred (particularly New York City Transit)
Interested candidates should send their resume and desired salary rate to email@example.com.
Job Function Summary:
Responsible for providing leadership, managing, planning, executing and reporting on regulated Quality Assurance activities for internal/external audits. This individual is responsible for performing Internal, domestic and international audits(as appropriate) that ensure compliance with the FDA QSR, ISO, MDD, CMDR requirements, and other worldwide health authority regulations/guidelines, site SOPs, protocols, and industry standards, as applicable. The Auditor acts as a compliance resource and provides recommendations for corrective action and tracks corrective action commitments until closure.
Continue reading Senior Quality Engineer – Healthcare company