Joby George

Product manager

Joby George is a product manager at Sparta Systems, developer of quality management software solutions. George has been with Sparta for more than 11 years with experience in the support, services, and pre-sales organizations. He has lead the effort on various TrackWise solutions, such as the Electronic Regulatory Report and TrackWise Analytics. Currently his primary responsibility is leading and defining the product and development efforts for  Stratas SaaS-based solutions. George has bachelor of science degrees in computer science and economics from Rutgers University in New Brunswick, New Jersey.

Tue, 11/03/2009 - 07:32
Don’t Let Ineffective Quality Management Drag You Down Take these first three steps toward an EQMS solution
Fri, 10/28/2016 - 14:51
Having difficulty managing quality and quality-related data? You’re not alone. Many manufacturers struggle with this these issues due to paper-based or other disparate systems being used to track, manage, and report on quality events. Walk about a…
Ensuring Quality and Efficiency Across the Supply Chain Once again, Deming’s philosophy rings true
Thu, 09/22/2016 - 11:56
Manufacturing has changed dramatically during the past several years. Where once original equipment manufacturers made products primarily within their own four walls, now those companies must manage a complex global supply chain. In an effort to…
Four Steps to Build a Quality Network Through Improved Supplier Management Linking suppliers increases visibility, efficiency, and safety
Wed, 04/13/2016 - 10:06
Driven by market expansion, financial pressures, and the need to accelerate innovation, today’s manufacturers have expanded their global operations and supply partners. This evolution has only amplified the manufacturer and supply-chain…
Electronic Medical Device Reporting Best Practices Steps for a smooth transition from paper-based reporting
Tue, 11/03/2009 - 07:32
The FDA’s Center for Devices and Radiological Health (CDRH) posted a notice of draft guidance that will require all medical device adverse-event reports to be submitted electronically. While the process of electronic submission of data is a more…