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Sinead Egan Location
Ireland
Sinead Egan Work
Director of Regulatory Affairs @ (August 2026 - Present)
Director, Regulatory Affairs, CIRL @ (January 2021 - August 2026)
Senior Business Manager @ (September 2019 - January 2021)
Regulatory Affairs Manager @ (July 2015 - September 2019)
Project Manager (Technical Files) @ (September 2013 - July 2015)
Senior Post Market Surveillance Specialist @ (September 2011 - August 2013)
Regulatory Affairs Specialist @ (October 2006 - October 2011)
Study lead @ (May 2004 - September 2006)
Sinead Egan Education
National University of Ireland, Galway and IT Sligo
Master's degree (Medtech Regulatory Affairs)
2016-2018
Technological University Dublin
Physics and Physics Technology (Physics)
1996-2002
Sinead Egan Skills
Design Control
ISO 14971
Chemistry
GMP
IVD
Med Dev 2.12 1
Regulatory Affairs
Change Control
Validation
Medical Devices
Quality Assurance
Strategic Planning
Corrective And Preventive Action Capa
Medical Device Directive
Quality System
V&V
Cross Functional Team Leadership
Customer Service
U.S. Food And Drug Administration Fda
98/79/Ec
Regulatory Submissions
SQL
Ivdd
Project Management
Science
Marketing Strategy
CAPA
FDA
21 CFR Part 11
ISO 13485
Verification And Validation V&V
Regulatory Requirements
u.s. Food and Drug Administration
Corrective and Preventive Action
Verification and Validation
Sinead Egan Summary
Sinead Egan, based in Ireland, is currently a Director of Regulatory Affairs at Perfuze. Sinead Egan brings experience from previous roles at Cook Medical and Teleflex Incorporated. Sinead Egan holds a 2016 - 2018 Master's degree in Medtech Regulatory Affairs @ National University of Ireland, Galway and IT Sligo. With a robust skill set that includes Design Control, ISO 14971, Chemistry, GMP, IVD and more. Sinead Egan has 2 emails on RocketReach.
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