Scott Cameron

Skills

Quality System Implementation, ISO 13485 Certification, Supplier Relations, Supplier Contracts, Project Management, Budget Forecasting, Transfer Products to Manufacturing, Commercial Manufacturing Process Development, Risk Analysis, Hazard Analysis, Manufacturing Process Definition, Manufacturing Process Qualification and Validation, Root Cause Analysis, Design Controls, Risk Management

About

With 30 years of product design in the Medical Device, Bio-Tech and Pharma-Tech industries, I am an SME in device design, development and product lifecycle management. I have 20 years of management experience in device engineering, manufacturing operations, quality and regulatory which provides a well-rounded perspective working with cross-functional teams. As a result, I’ve been an effective leader and mentor in delivering technical data driven solutions to these areas of expertise.