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Developing and Managing Supplier Quality Agreements: An Introduction

  June 05, 2013  
CfPA - The Center for Professional Advancement, 90 Minute Accredited Online Training
July 16, 2013 at 11:00 a.m.–12:30 p.m. (ET)

Who Should Attend
This online course is designed for Medical Device, Pharmaceutical and other Life Science professionals who develop or manage agreements with suppliers in the medical device industry. This includes, but is not limited to, professionals in Supplier Quality, Supply Chain Management, Procurement, and Supplier Quality Assurance.

You will gain valuable knowledge on developing and managing supplier quality agreements from two leading experts who have joined forces to present this 90 minute course. James Shore and John Freije have over 40 years combined working experience with suppliers and developing agreements.

This course will be available On Demand: July 17, 2013

This 90-minute accredited online training course provides comprehensive and up-to-date knowledge of developing and managing supplier agreements. The course covers regulatory expectations regarding supplier agreements contained in U.S. and International regulations and guidelines. This course will prepare attendees to effectively develop and manage supplier agreements.


Organized by: CfPA - The Center for Professional Advancement
Invited Speakers: John Freije, CQE, CMfgT, Freije Quality Engineering

John Freije, CQE, CMfgT has spearheaded Freije Quality Engineering’s consulting services since 2007. Freije Quality Engineering, LLC, is a fullservice consulting firm providing clients with quality system and regulatory affairs consulting.

Mr. Freije has over 30 years experience working for the government and the private sector, with 20 years in the medical device and pharmaceutical industries. Previously he helped revamp Roche Diagnostics’ purchasing process due to an unfavorable Warning Letter in 2004. Other experience includes supporting projects for the Special Forces and Direct Fire Control at Raytheon Technical Services Company and various Engineering and Quality positions at Eli Lilly supporting medical device commercialization, quality, and manufacturing, bulk manufacturing for injectables and dry products manufacturing for clinical trials.

Honorably discharged after serving eight years in the Ordnance Corps in the US Army as a Field Artillery Systems Mechanic, he is an active member of SME and ASQ and holds the position of Treasurer for the ASQ Biomedical Division.

James Shore, Operations Manager/Continuous Improvement Manager, Dynisco

James Shore has 25 years in Quality and Supplier Management working in medical devices as well as other various industries such as semiconductor capital equipment, aerospace/defense contractor. He is currently the Product/Process Improvement Leader at Dynisco in Franklin, MA responsible for the implementation of the global material replenishment program and the manufacturing of a new product line. Previously. he worked with Boston Scientific on new product development programs and with the Corporate Supplier Quality team on various medical device Product Development projects for the Endoscopy, Oncology and Cardio Divisions.

His professional certifications include ASQ Certified Six Sigma Black Belt (SSBB), ASQ Certified Quality Manager (CQM), Certified Quality Auditor (CQA) and Certified Mechanical Inspector (CMI) and ASQ Senior Member. A Certified Welding Inspector (CWI) from the American Welding Society, he now has Lean Bronze certification from the Association for Manufacturing Excellence (AME). Mr. Shore is a Desert Storm Veteran (1991) and was Honorably discharged at the rank of Gunnery Sergeant (E-7) from the US Marine Corps.
Deadline for Abstracts: n/a
Registration: Please click here for registration information.
E-mail: sberg@cfpa.com
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