LeMaitre
A Regulatory Affairs Manager develops and implements documentation policies for cardiovascular devices, ensuring compliance with US and international regulatory agencies. The role involves preparing regulatory submissions, guiding product development teams on filing activities, and maintaining knowledge of new regulatory developments.
Headquarters
Burlington, Massachusetts, United States
Company Size
501-1000 employees
Founded
1983
LeMaitre is a medical device company that develops, manufactures, and supplies specialized products for vascular surgeons and endovascular interventions. Their portfolio includes surgical instruments, catheters, vascular grafts and related accessories—built through ongoing research and clinician collaboration to address the needs of modern vascular care. Serving hospitals and clinics globally, LeMaitre emphasizes innovation, clinical evidence, and surgeon-focused solutions to improve patient outcomes.
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
View leadership team, funding history,
and employee contacts for LeMaitre.
16% below the average for this role
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