Gene David Redig

Director Quality and Regulatory Consulting

We found the following information about Gene David Redig at MyRAQA, where this professional has worked as a Sr. Director since 2010. Gene's total work experience is over 14 years, during which time Gene David Redig had at least nine jobs at different companies to develop professional skills. Gene studied at the University of Minnesota - Carlson School of Management to 1989. This person received the following certifications: Certified Quality Manager (Cqm), Certified Software Quality Engineer (Csqe), and Certified Quality Auditor (Cqa). Gene David Redig is proficient in English. Currently, Gene David Redig lives in Novato, California. You can contact with Gene by searching for phone or email or get additional info by requesting access to this professional's additional details.
Name variants:
Eugene Redig, Eugenia Redig, Genevieve Redig

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Contact Information

Last Update
Jun 30, 2022
Email
ge**@comcast.net, eu**@excite.com
Location
Novato, CA
Company

Workplace

Myraqa, Inc.
Sr. Director

Industry

Medical Devices

Work History

Sr. Director

Myraqa is a full-service IVD Regulatory consulting firm. Founded in 1998 as a solo practice, Myraqa has grown to include leading experts in RA, QA, Design Control, Process Development, Syst...
from Oct 2010

Consultant

While consulting for Volcano Corporation, I helped manage the quality and regulatory aspects for this medical device company to ensure that the operational business was in compliance with cG...
Oct 2009 — Oct 2010

Consultant

While consulting for J-PAC, LLC, I helped manage the quality and regulatory aspects for this medical device company to ensure that the operational business was in compliance with cGMP, regul...
Jun 2009 — Oct 2009

Consultant

While consulting for Medtronic CoreValve, I helped manage the quality and regulatory aspects for this medical device company to ensure that the operational business was in compliance with cG...
May 2009 — Jun 2009

Director, Regulatory Compliance

Intuitive Surgical, Inc. (Nasdaq: ISRG) is the global technology leader in robotic-assisted minimally invasive surgery (MIS). The Company's da Vinci® Surgical System offers surgeons superio...
Aug 2008 — Jan 2009

VP, Quality and Regulatory Affairs

Circle Medical Devices (CMD) is a Medical Device Engineering Services and Contract Manufacturing firm with extensive experience in bringing medical devices to market. CMD offers expertise i...
Jan 2008 — Jul 2008

Director of Quality

Integrated Biosystems, now part of Sartorius Stedim Biotech, supplies Controlled Freeze-Thaw technology solutions to the biopharmaceutical manufacturing industry. Sartorius Stedim Biotech i...
May 2004 — Oct 2007

Quality Manager

Mallinckrodt, now part of Tyco Healthcare, manufactures and markets medical products.
May 1996 — Oct 2000

Corporate Quality Sr. Staff Specialist

A leader in medical technology - alleviating pain, restoring health, and extending life for people around the world.
Sep 1991 — May 1996

Occupations

Executive
Director
Counselor
Operations Manager
Advisor

Skills

Fda
Medical Devices
Quality System
Quality Assurance
Cross Functional Team Leadership
Design Control
Iso 13485
V&V
Regulatory Affairs
Biotechnology
Product Development
Gmp
R&D
Quality Management
Iso
Validation
Commercialization
Testing
Six Sigma
Capa
Process Improvement
21 Cfr Part 11
Lean Manufacturing
Healthcare
Fmea
User Acceptance Testing
Continuous Improvement
Documentation
Auditing
Compliance
Risk Management
Test Planning
System Testing
Problem Solving
Usability Engineering
Test Cases
Test Strategy
Test Automation
Regression Testing
Manual Testing
Test Management
Quality Engineering
Quality Systems
Specs
Action Plans
Process Development
Cgmp
Process Validation
Qsr
Diagnostics
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