Eric Davis

About Eric Davis

Quality Engineering. Regulatory Affairs. Software and Hardware Testing. Technical Writing and Editing. The majority of my career has been in the medical device industry. Complaint handling and audit preparation. Software quality assurance and testing experience in a wide variety of environments. Functionality, compatibility, reliability, usability, installation, Comfortable working solo and in a team environment. Extensive training in software testing theories and procedures. Technical writing user, service, and marketing documentation. Communicate well with all levels of personnel. Superior organizational skills and ability to handle many projects simultaneously.

Experience

1. Associate Director, Quality Systems at Exact Sciences

   Exact Sciences

   Dec 2020 — Present

   Responsible for management and continuous improvement of the Global Quality System. The position is also responsible for working collaboratively with teams that Quality supports to ensure appropriate establishment and maintenance of technical processes, procedures and work instruction, and administration in the implementation and maintenance of documentation processes in accordance with Good Manufacturing Practices. Primary responsibilities include the implementation and administration of quality processes, records, and data projects, such as assurance of proper record control. Additional responsibilities include system administration for eQMS, eLMS, and management of the training program.

Education

• Madison Area Technical College

  AA, Liberal arts

  1993 — 1995

• University of Wisconsin-Madison

  BA, English

  1996 — 1998

Skills

• Medical Devices
• Software Documentation
• Quality Assurance
• Testing
• Quality System
• Fda
• Technical Writing
• Iso 13485
• Validation
• Process Improvement
• Cross-Functional Team Leadership
• Product Development
• Design Control
• Calibration
• Electronics
• Regulatory Affairs
• Capa
• Software Quality Assurance
• V&V
• Field Service
• Manufacturing
• Medical Imaging
• Hardware Diagnostics
• R&D
• Six Sigma
• Change Control
• Visio
• Product Launch
• Biomedical Engineering
• Training
• 21 Cfr Part 11
• Continuous Improvement
• Design of Experiments
• Dmaic
• Databases
• Technical Support
• Quality Control
• Fmea
• Quality Management
• Iso