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Gary Barrett Email & Phone Number

Head of Global Regulatory Affairs | VP Regulatory Affairs, at Convatec
Location: Minneapolis, Minnesota, United States 8 work roles 1 school
1 work email found @convatec.com LinkedIn matched
✓ Verified August 2026 4 data sources Profile completeness 100%

Contact Signals · 1 work email

Work email g****@convatec.com
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Current company
Role
Head of Global Regulatory Affairs | VP Regulatory Affairs,
Location
Minneapolis, Minnesota, United States

Who is Gary Barrett? Overview

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Quick answer

Gary Barrett is listed as Head of Global Regulatory Affairs | VP Regulatory Affairs, at Convatec, based in Minneapolis, Minnesota, United States. AeroLeads shows a work email signal at convatec.com and a matched LinkedIn profile for Gary Barrett.

Gary Barrett previously worked as Head of Global Regulatory Affars at Convatec and VP Regulatory Affairs, Quality Systems and Compliance at Smiths Medical Limited. Gary Barrett holds Phd, Biotechnology - Biosensor Development from Cranfield University.

Company email context

Email format at Convatec

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{first}.{last}@convatec.com
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AeroLeads found 1 current-domain work email signal for Gary Barrett. Compare company email patterns before reaching out.

Profile bio

About Gary Barrett

Leading the Global Regulatory Affairs at Convatec, my role is centered around deploying my expertise in international regulatory affairs and analytical skills to navigate complex regulatory landscapes. Our team's efforts have been pivotal in ensuring compliance and market access for cutting-edge medical devices, positively impacting patient care internationally. Previously, as VP of Regulatory Affairs at Smiths Medical, I honed my skills in new business development while managing quality systems and compliance. There, we succeeded in remediating multiple critical regulatory challenges, safeguarding $100 million in sales and closing out six warning letters, thanks to our collective dedication and strategic approach.

Listed skills include Medical Devices, Iso 13485, Regulatory Affairs, Ce Marking, and 20 others.

Current workplace

Gary Barrett's current company

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Convatec
Convatec
Head of Global Regulatory Affairs | VP Regulatory Affairs,
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8 roles

Gary Barrett work experience

A career timeline built from the work history available for this profile.

Head Of Global Regulatory Affars

Current

London, England, Gb

Nov 2020 - Present

Vp Regulatory Affairs, Quality Systems And Compliance

Head of regulatory affairs and quality systems.

Apr 2018 - Nov 2020

Snr Vp Qa Ra

Latham, New York, Us

Jun 2015 - Apr 2018

Vp Ra Qa

Latham, New York, Us

May 2014 - Jun 2015

Snr Project Manager

Milan, It

Notified Body auditor for CE marking of medical devices. Medical Device Directive, ISO 13485, CMDCAS.

Mar 2006 - Sep 2010
1 education record

Gary Barrett education

  • Cranfield University
    Cranfield University
    Biotechnology - Biosensor Development
FAQ

Frequently asked questions about Gary Barrett

Quick answers generated from the profile data available on this page.

What company does Gary Barrett work for?

Gary Barrett works for Convatec.

What is Gary Barrett's role at Convatec?

Gary Barrett is listed as Head of Global Regulatory Affairs | VP Regulatory Affairs, at Convatec.

What is Gary Barrett's email address?

AeroLeads has found 1 work email signal at @convatec.com for Gary Barrett at Convatec.

Where is Gary Barrett based?

Gary Barrett is based in Minneapolis, Minnesota, United States while working with Convatec.

What companies has Gary Barrett worked for?

Gary Barrett has worked for Convatec, Smiths Medical Limited, Angiodynamics, Dekra Certification B.V., and Merit Medical Systems, Inc..

How can I contact Gary Barrett?

You can use AeroLeads to view verified contact signals for Gary Barrett at Convatec, including work email, phone, and LinkedIn data when available.

What schools did Gary Barrett attend?

Gary Barrett holds Phd, Biotechnology - Biosensor Development from Cranfield University.

What skills is Gary Barrett known for?

Gary Barrett is listed with skills including Medical Devices, Iso 13485, Regulatory Affairs, Ce Marking, Medical Device Directive, Quality Assurance, Quality System, and Fda.

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