Rod Rylands Email & Phone Number

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Vice President Quality Assurance and Regulatory Affairs @ (March 2026 - Present)
Sr. Director Quality Assurance and Regulatory Affairs @ (April 2019 - November 2025)
QA and RA CONSULTANT @ Quality Assurance and Regulatory Affairs Consulting (January 2017 - October 2018)
VICE PRESIDENT - GLOBAL QUALITY ASSURANCE | COMPLIANCE @ (January 2014 - January 2017)
VICE PRESIDENT - GLOBAL QUALITY ASSURANCE - REGULATORY AFFAIRS | COMPLIANCE @ Verathon Medical (January 2013 - January 2014)
VICE PRESIDENT - GLOBAL QUALITY | COMPLIANCE @ (January 2010 - January 2013)
VICE PRESIDENT - GLOBAL QUALITY | REGULATORY AFFAIRS @ Roche Tissue Diagnostics (January 2009 - January 2010)

Carnegie Mellon University
Graduate School of Industrial Administration (Program for Executives)
University of Pittsburgh
BS (Biology)

Global Regulatory Compliance – 21 CFR, ISO 9000, 13485, 14971, IEC 62304, EU MDD and MDR, etc.
Quality System Excellence
Quality System Development
Quality Assurance
ISO 13485
Regulatory Affairs
FDA
Medical Devices
CAPA
Quality System
Design Control
V&V
21 CFR Part 11
Validation
Change Control
Strategic Planning
GMP
Quality Management
Sop
Quality Control
Biotechnology
Regulatory Submissions
ISO
R&D
Regulatory Requirements
Biopharmaceuticals
Lifesciences
Clinical Trials
Life Sciences
Quality Auditing
Pharmaceutical Industry
U.S. Food and Drug Administration (FDA)
GLP
Root Cause Analysis
Research and Development (R&D)
Corrective and Preventive Action (CAPA)
Verification and Validation (V&V)
Technology Transfer
Clinical Development
LIMS
Cross-functional Team Leadership
PMA
ISO 14971
FDA GMP
Computer System Validation
CE marking
Medical Device Directive
21 CFR
Complaint Management
GxP
Verification And Validation V&V
Corrective And Preventive Action Capa
Strategy
Research And Development R&D
Microsoft Office
Microsoft Excel
Cross Functional Team Leadership
U.S. Food And Drug Administration Fda
Sales
Research and Development
Corrective and Preventive Action
u.s. Food and Drug Administration
Verification and Validation

Rod Rylands, based in Denver, CO, US, is currently a Vice President Quality Assurance and Regulatory Affairs at Vaporox Inc.. Rod Rylands brings experience from previous roles at Henry Schein, Quality Assurance and Regulatory Affairs Consulting, Physio-Control, now part of Stryker and Verathon Medical. Rod Rylands holds a Graduate School of Industrial Administration in Program for Executives @ Carnegie Mellon University. With a robust skill set that includes Global Regulatory Compliance – 21 CFR, ISO 9000, 13485, 14971, IEC 62304, EU MDD and MDR, etc., Quality System Excellence, Quality System Development, Quality Assurance, ISO 13485 and more. Rod Rylands has 3 emails and 2 mobile phone numbers on RocketReach.