COMPLIANCE TRAINING WEBINAR ON LEAN DOCUMENTS, DOC 2015 - An Advanced Course on Lean Documents, Lean Configuration and Document Control

Website http://bit.ly/1DRObl7 | Edit Freely

Category FDA Compliance;

Deadline: February 27, 2015 | Date: February 27, 2015

Venue/Country: Palo Alto, U.S.A

Updated: 2015-02-25 15:02:30 (GMT+9)

Call For Papers - CFP

Why Should You Attend:

Just as a manufacturing process produces a product, controlled documents are the product of a business process. Just as in manufacturing, a product cannot move forward if it is waiting for component parts, a document cannot move forward if it is waiting for information, or if its use is constrained by other documents.

Who Will Benefit:

This webinar will provide valuable insights to:

Design engineers

Manufacturing engineers

Operations managers

Quality system managers

Document control managers

Instructor Profile:

Jose Mora, is a Principal Consultant specializing in Manufacturing Engineering and Quality Systems. For over 30 years he has worked in the medical device and life sciences industry specializing in manufacturing, process development, tooling, and quality systems. Prior to working full time as a consulting partner for Atzari Consulting, Jose served as Director of Manufacturing Engineering at Boston Scientific and as Quality Systems Manager at Stryker Orthopedics, where he introduced process performance, problem solving, and quality system methodologies.

Use coupon code 232082 and get 10% off on registration.