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Sarah Deegan
Sarah Deegan
VP QA/RA | Johnson & Johnson
Ireland
Sarah Deegan
Summary
Sarah Deegan is a seasoned executive with over two decades of experience in quality assurance and regulatory affairs within the medical device industry. Currently serving as the Worldwide Vice President of Quality and Regulatory at DePuy, she has a proven track record of leadership in high-stakes environments. Her expertise spans a range of critical areas including FDA regulations, ISO standards, and continuous improvement methodologies. Sarah's career includes significant roles at industry giants such as Johnson & Johnson and Medtronic, where she has driven quality and compliance initiatives. Her educational background from Regis College has equipped her with a strong foundation in biomedical engineering principles. Passionate about advancing healthcare technology, she is committed to ensuring that products meet the highest quality standards. Sarah is known for her strategic thinking and ability to foster cross-functional collaboration. She is also an advocate for innovation in regulatory practices, aiming to streamline processes while maintaining safety and efficacy. Outside of her professional pursuits, she enjoys mentoring emerging leaders in the field.
Sarah Deegan
Work Experience
VP QA/RA at
Johnson & Johnson
January 1997 - Present
WW VP Quality and Regulatory at
DEPUY SA
Present
Director QA/RA/CA at
Medtronic
January 1992 - January 1997
Sarah Deegan
Education
January 1979 - January 1983
Frequently Asked Questions about Sarah Deegan
What company does Sarah Deegan work for?
Sarah Deegan is a VP QA/RA at Johnson & Johnson, a company specializing in Specialty hospitals, except psychiatric.
Where Sarah Deegan graduated from?
Sarah Deegan holds a degree in from Regis College.
Who is Sarah Deegan?
Sarah Deegan is a seasoned executive with over two decades of experience in quality assurance and regulatory affairs within the medical device industry. Currently serving as the Worldwide Vice President of Quality and Regulatory at DePuy, she has a proven track record of leadership in high-stakes environments. Her expertise spans a range of critical areas including FDA regulations, ISO standards, and continuous improvement methodologies. Sarah's career includes significant roles at industry giants such as Johnson & Johnson and Medtronic, where she has driven quality and compliance initiatives. Her educational background from Regis College has equipped her with a strong foundation in biomedical engineering principles. Passionate about advancing healthcare technology, she is committed to ensuring that products meet the highest quality standards. Sarah is known for her strategic thinking and ability to foster cross-functional collaboration. She is also an advocate for innovation in regulatory practices, aiming to streamline processes while maintaining safety and efficacy. Outside of her professional pursuits, she enjoys mentoring emerging leaders in the field.
Sarah`s contact details
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