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LeMaitre

Global provider of vascular surgery devices.

Manager – Product Life Cycle Engineering

Biomedical Engineering & Medical DevicesPosted on Nov 5
Full-timeBurlington, MA, USA

About the Job

Requirements

  • A Bachelor's degree in a technical field is required; a focus in Biomedical Engineering is preferred.
  • At least four years of relevant work experience is required.
  • At least three years of product development experience is required, with a proven track record directly associated with or leading efforts to develop technically sophisticated products from concept to market.
  • Strong problem-solving and execution skills are required to develop creative solutions and meet project objectives.
  • Ability to balance schedule, cost, and quality is required.
  • Detailed knowledge of new product development processes and/or change management methodologies in a medical device setting is required.
  • A consistent track record of delivering project outcomes in an ambiguous environment is required.
  • Experience leading self-directed work teams is required.
  • Working knowledge of ISO 13485, ISO 14971, and FDA GMP/QSR is required.
  • The employee is required to work onsite at the Burlington, Massachusetts office.
  • Up to 10% domestic and international travel is required.

Responsibilities

  • Manage Product Life Cycle Engineers, currently two direct reports.
  • Develop or revise testing protocols and reports to support continued regulatory compliance with existing and revised industry standards for Class I, II, and III medical devices.
  • Engage with Regulatory Affairs and Quality Affairs teams to ensure all standards are current and fully applied to products.
  • Conduct gap assessments on product technical documentation and recommend improvements.
  • Initiate change orders or guide cross-functional groups in implementing changes.
  • Participate in the CAPA process as it relates to product conformance.
  • Partner with multifunctional leaders to ensure alignment, efficiency, and execution meet business requirements.
  • Ensure the voice of the customer is represented in decisions and design requirements are translated into practical design changes that can be verified and validated in manufacturing.
  • Ensure projects comply with regulatory requirements, including GMP, ISO, and MDD/MDR, and with company policies and procedures.
  • Capture and disseminate knowledge gained during projects to improve product development processes and systems.
  • Acquire resources from functional organizations, support groups, and outside sources to ensure project success.
  • Provide assistance in related areas when needed.

Desired Qualifications

  • Strong communication, teamwork, and influencing skills.

About the Company

LeMaitre

Global provider of vascular surgery devices.

LeMaitre develops and sells vascular surgery medical devices worldwide, focusing on treatments for peripheral vascular disease. Its LeMaitre Valvulotome lets surgeons cut valves in peripheral veins without direct vision, while its broader portfolio includes aortic grafts, vascular allografts, occlusion catheters, AV access systems, and collagen grafts. The company differentiates itself through a focused vascular-device portfolio, a global footprint in 90 countries, and a track record of clinically useful, high-quality products trusted by surgeons. Its goal is to improve vascular treatment outcomes by expanding access to reliable devices and advancing surgical tools through ongoing research and development.

Company size
501-1,000
Company stage
IPO
Headquarters
Burlington, MA
Founded
1983

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