LeMaitre Vascular in Burlington, MA is seeking an Engineer to lead Product Life Cycle activities for medical devices, including development and revision of testing protocols to ensure GMP, ISO13485 and FDA compliance. The role oversees 2 direct reports, collaborates with Regulatory and Quality teams, drives change management, and translates customer needs into verifiable design changes for manufacturing.
The position emphasizes cross-functional leadership, CAPA participation, risk management,
#J-18808-LjbffrLead Product Lifecycle Engineer, Regulated Medical Devices in burlington at Unknown Company
This position is listed as full time and onsite.