Global Q, Inc. is a computer software company offering a cloud-based Quality Management Platform as a Service (PaaS). As Co-founder, John applied his years of experience in medical device Quality Management Systems to design and optimize the Optiqs360 eQMS Platform.

Responsible for the Design Quality Assurance and Health Hazard Evaluation processes at Zimmer Biomet for the Knee, Hip, Biologics, Extremities, Sports Medicine and Trauma business segments. He lead an organization fo 50+ Quality Managers, Engineers and Technicians across 6 global sites.

Proven leadership of Medical Device Quality Management in positions of increasing scope andresponsibility.Fiscal authority and responsibility for a $24M+ budget managing an organization of 220+ teammembers spanning 6 global sites.Front room Audit Leader for numerous FDA / ISO inspections with hundreds of hours of Auditorinteraction experience.Co-author of the Corporate Design Control / Risk Management System policies and procedures forthe merger of Zimmer and Biomet Quality Management Systems.Zimmer Biomet merger Integration Leader for Global Quality / Regulatory / Clinical organizationalstructure optimization.Quorum member of the Product Safety Review Board and Global Recall Committee with hundreds ofhours of experience making critical product safety decisions relating to fielded products.Quality Systems Due Diligence Leader on multiple due diligence audits of potential acquisitiontargets.Executive Steering Committee Member of multiple FDA 483 response remediation projects spanningDesign History Files, Complaint Files and Corrective and Preventive Actions.

Upon promotion to Director, John assumed responsibility for Design, Operations and Supplier Quality Assurance of the Knee, Hip, Bone Cement, Biologics, Sports Medicine, Extremities, Foot and Ankle and Trauma Business Units. He lead department of 125+ Quality Managers, Engineers, Supervisors, Technicians and Inspectors Team in the execution of all Quality Management System requirements. John also lead front room audit facing for 2 FDA and multiple ISO inspections, and lead Product Safety Review Board and Recall Committee meetings.

In this role, John was responsible for Quality Engineering of the Knee, Hip, Bone Cement, Biologics, Sports Medicine, Extremities, Foot and Ankle and Trauma business units. He lead a department of 12+ Quality Engineers in the execution of Design Control, Risk Management, and CAPA processes.

Upon promotion to Quality Assurance Manager, John assumed responsibility for Plant Quality Assurance of the Needle and Syringe business unit. He lead a department of 60+ Quality Engineers, Supervisors, Technicians and Inspectors in the execution of all Quality Management System requirements in the production and on-site gamma sterilization of over 1 Billion needles annually. John also ran the front room audit for 2 FDA and multiple ISO inspections.

In this role, John was responsible for Quality Engineering of the Kendall Sharps Container and Magellan Safety Needle business units. He lead a team of Quality Technicians to execute all Quality Management System requirements.

SunEdison is a renewable energy company that develops, builds, owns, and operates solar power plants and wind energy plants. It also manufactures high purity polysilicon, monocrystalline silicon ingots, silicon wafers, solar modules, solar energy systems, and solar module racking systems. John was responsible for product development and process optimization of the 300mm silicon wafer line. In his role as Senior Development Engineer, he developed an optimized wire saw process and launched a new manufacturing facility in Japan, resulting in an 8% reduction in 300mm wafer scrap from wire saw defects.