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Eugene Helsel

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Eugene Helsel

Senior Vice President, Regulatory Affairs | Artiva Biotherapeutics

Del Mar, California, United States

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Eugene Helsel

Summary

Eugene Helsel is a seasoned professional with over 30 years of experience in the biotech industry, specializing in regulatory affairs and quality assurance. As the Senior Vice President of Regulatory Affairs at Artiva Biotherapeutics, he leads teams that support clinical development for innovative cell and gene therapies. His extensive expertise includes navigating complex regulatory environments and ensuring compliance with FDA and international standards. Eugene has a strong educational background in Manufacturing Engineering and Psychology, which complements his analytical and leadership skills. He has worked with various biotech firms, enhancing their regulatory strategies and ensuring successful product submissions. His career reflects a commitment to advancing therapeutic technologies while maintaining rigorous quality standards. Eugene is passionate about mentoring the next generation of regulatory professionals and is actively involved in industry discussions on best practices. His ability to adapt to evolving regulatory landscapes makes him a valuable asset in the biotech sector.

General

Specialist

Technical Background

Leadership Experience

Long-Term Tenure

Professional interests

Emerging Technologies

Leadership Development

Innovation

Organisational experience

Startup Experience

Corporate Experience

Consulting Experience

Eugene Helsel

Work Experience

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Senior Vice President, Regulatory Affairs at

Artiva Biotherapeutics

February 2024 - Present

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Vice President, Regulatory Affairs and Quality at

Artiva Biotherapeutics

August 2019 - February 2024

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Principal Consultant at

Halloran Consulting Group, Inc.

September 2018 - August 2019

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Senior Director, Regulatory Affairs at

Capricor Therapeutics, Inc.

January 2018 - June 2018

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Executive Director, Regulatory Affairs and Quality at

Fate Therapeutics Inc.

December 2015 - October 2017

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Senior Director, Regulatory Affairs at

Fate Therapeutics Inc.

June 2014 - December 2015

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Regulatory Affairs Consultant at

Anjon Biologics

June 2013 - June 2014

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Regulatory Affairs Consultant at

Celavet Biosciences

January 2013 - June 2014

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Regulatory Affairs and Quality Consultant at

VTI

February 2014 - May 2014

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Quality Consultant at

Pyramid Labs

October 2013 - December 2013

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Quality Consultant at

Crisi Medical Systems

June 2013 - August 2013

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Regulatory Affairs Consultant at

Evofem Biosciences

January 2013 - June 2013

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Vice President, Regulatory Affairs and Quality at

Evofem Biosciences

August 2011 - January 2013

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Senior Director, Quality at

Stemedica Cell Technologies, Inc

April 2009 - August 2011

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Regulatory Affairs and Quality Assurance Consultant at

Biomed

July 2008 - April 2009

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Director, Quality Assurance at

SANG.art

May 2006 - July 2008

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Senior Director of Quality and Regulatory Compliance at

Validation Technologies

December 2002 - March 2006

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Regulatory Affairs and Quality Consultant at

SeQual Technologies

February 2001 - April 2002

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Eugene Helsel

Education

, Bs

January 1988 - January 1990

University of California, San Diego, Ba

January 1980 - January 1983

De Anza Junior College

January 1977 - January 1979

Abington Friends School

January 1971 - January 1977

Frequently Asked Questions about Eugene Helsel

What is Eugene Helsel email address?

Eugene Helsel's primary email address is *******@artivabio.com. To view the full verified email and additional contact details, sign up for free with Muraena.

What company does Eugene Helsel work for?

Eugene Helsel is a Senior Vice President, Regulatory Affairs at Artiva Biotherapeutics, a company specializing in Commercial physical research.

Where Eugene Helsel graduated from?

Eugene Helsel holds a degree in Manufacturing Engineering from null.

How can I directly contact Eugene Helsel?

To contact Eugene Helsel directly, you can use the email address *******@artivabio.com. Complete contact information is available upon registration with Muraena.

Who is Eugene Helsel?

Eugene Helsel is a seasoned professional with over 30 years of experience in the biotech industry, specializing in regulatory affairs and quality assurance. As the Senior Vice President of Regulatory Affairs at Artiva Biotherapeutics, he leads teams that support clinical development for innovative cell and gene therapies. His extensive expertise includes navigating complex regulatory environments and ensuring compliance with FDA and international standards. Eugene has a strong educational background in Manufacturing Engineering and Psychology, which complements his analytical and leadership skills. He has worked with various biotech firms, enhancing their regulatory strategies and ensuring successful product submissions. His career reflects a commitment to advancing therapeutic technologies while maintaining rigorous quality standards. Eugene is passionate about mentoring the next generation of regulatory professionals and is actively involved in industry discussions on best practices. His ability to adapt to evolving regulatory landscapes makes him a valuable asset in the biotech sector.

Eugene`s contact details

mail

*******@artivabio.com

*******@raps.org

Colleagues

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Nicholas Veomett

Vice President of Corporate Development & AlloNK Program Lead

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Thorsten Graef

Chief Medical Officer

Chris Horan

Chief Technical Operations Officer

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Cliff Wallace

Executive Director of Quality

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Heather Raymon

Senior Vice President, Research and Early Development

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Jennifer Bush

Chief Operating Officer

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Amanda Medcalf Conerty

Executive Director, Process, Analytical Development and Manufacturing

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