Zachary Woodson

Vice President of Regulatory Affairs and Quality

We found the following information about Zachary Woodson at Claret Medical, where Zachary Woodson has worked as a Vice President of Quality Assurance and Regulatory Affairs since 2015. Zachary's total work experience is over 19 years, during which time they had at least eight jobs at different companies to develop skills. Zachary attended school at the Sonoma State University from 1997 to 2001. Zachary Woodson can be found in San Francisco, California – where this expert is currently located. You can search for the professional's phone and email. We can also provide you detailed contact information upon request.
Name variants:
Zachariah Woodson, Zacharias Woodson, Zackary Woodson, Zack Woodson, Zacky Woodson, Zach Woodson
Last updated Jun 26, 2024

Contact Information

Last Update
Jul 13, 2022
Email
za**@medtronic.com
Location
San Francisco, CA
Company

Workplace

Vice President of Quality Assurance and Regulatory Affairs

Santa Rosa, CA

Industry

Medical Devices, Health/Allied Services, Whol Medical/Hospital Equipment

Work History

Vice President of Quality Assurance and Regulatory Affairs

3633 Westwind Blvd, Santa Rosa, CA 95403
Claret Medical is a Medical Device company located in 3633 Westwind Blvd, Santa Rosa, CA, United States.
Oct 2015 — Oct 2017

Vice President of Regulatory Affairs and Quality

from Oct 2017

Director of Regulatory Affairs

710 Medtronic Pkwy, Minneapolis, MN 55432
May 2013 — Oct 2015

Senior Regulatory Affairs Manager

710 Medtronic Pkwy, Minneapolis, MN 55432
Jun 2007 — Apr 2013

Senior Regulatory Affairs Manager

Feb 2005 — Jun 2007

Qa and Ra Consultant

Feb 2003 — Feb 2005

Regulatory Affairs Specialist

Jan 2000 — Feb 2003

Document Control Supervisor

1997 — 1999

Education

1997 — 2001
1973 — 1979

Occupations

Executive
Vice President
IT Professional
Software Tester
Chief Executive
Computer Specialist

Skills

Regulatory Affairs
Fda
Medical Devices
Iso 13485
Regulatory Submissions
Quality System
Design Control
Capa
Validation
V&V
Clinical Trials
Gmp
Commercialization
R&D
Iso 14971
Biotechnology
Biomedical Engineering
Clinical Development
U.s. Food and Drug Administration
Pharmaceutical Industry
Corrective and Preventive Action
Ce Marking
Pma
Verification and Validation
Regulatory Requirements
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