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Eugene Helsel
Eugene Helsel
Senior Vice President, Regulatory Affairs | Artiva Biotherapeutics
Del Mar, California, United States
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.
Eugene Helsel
Work Experience
Senior Vice President, Regulatory Affairs at
Artiva Biotherapeutics
February 2024 - Present
Vice President, Regulatory Affairs and Quality at
Artiva Biotherapeutics
August 2019 - February 2024
Principal Consultant at
Halloran Consulting Group, Inc.
September 2018 - August 2019
Senior Director, Regulatory Affairs at
Capricor Therapeutics, Inc.
January 2018 - June 2018
Executive Director, Regulatory Affairs and Quality at
Fate Therapeutics Inc.
December 2015 - October 2017
Senior Director, Regulatory Affairs at
Fate Therapeutics Inc.
June 2014 - December 2015
Regulatory Affairs Consultant at
Anjon Biologics
June 2013 - June 2014
Regulatory Affairs Consultant at
Celavet Biosciences
January 2013 - June 2014
Regulatory Affairs and Quality Consultant at
VTI
February 2014 - May 2014
Quality Consultant at
Pyramid Labs
October 2013 - December 2013
Quality Consultant at
Crisi Medical Systems
June 2013 - August 2013
Regulatory Affairs Consultant at
Evofem Biosciences
January 2013 - June 2013
Vice President, Regulatory Affairs and Quality at
Evofem Biosciences
August 2011 - January 2013
Senior Director, Quality at
Stemedica Cell Technologies, Inc
April 2009 - August 2011
Regulatory Affairs and Quality Assurance Consultant at
Biomed
July 2008 - April 2009
Director, Quality Assurance at
SANG.art
May 2006 - July 2008
Senior Director of Quality and Regulatory Compliance at
Validation Technologies
December 2002 - March 2006
Regulatory Affairs and Quality Consultant at
SeQual Technologies
February 2001 - April 2002
Eugene Helsel
Education
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
*******@artivabio.com
*******@raps.org
Colleagues
Vice President of Corporate Development & AlloNK Program Lead
Chief Medical Officer
Chief Technical Operations Officer
Executive Director of Quality
Senior Vice President, Research and Early Development
Chief Operating Officer
Executive Director, Process, Analytical Development and Manufacturing