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Manager, Product Life Cycle Engineering

Lemaitre Vascular INC - Burlington, MA, US

Posted May 5, 2026

Benefits

Parental leave
Not verified
Non-birth-parent leave
Not verified
Family-building benefits
  • Fertility benefits: Not verified
  • Adoption assistance: Not verified
  • Surrogacy assistance: Not verified
Mental health support
Not verified
Relocation assistance
Not verified
Childcare support
Not verified
Learning budget
Not verified
Verification
Not verified checked Jun 13, 2026
Salary
$130K-$175K From the posting source checked Jun 20, 2026
401(k) match
Reported from DOL Form 5500 industry filing (not employer-specific)

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Market context

U.S. role benchmark (BLS OEWS)
$102,662 U.S. median for this role
Projected growth (BLS Employment Projections)
+5.4% - Faster than average

49% above the BLS role benchmark for product management aggregate.

Matched to SOC 11-1021 - Product Management aggregate by role bucket.

Source: U.S. Bureau of Labor Statistics, OEWS, May 2024 and Employment Projections, 2024-2034.

Role

Role function
Product From the posting source checked Jun 20, 2026
Seniority
Mid From the posting source checked Jun 20, 2026

Schedule

Shift type
Not verified
Weekend work
Not verified

Company

Equity
Offered Verified - SEC 10-K source checked Jun 20, 2026

Application

Cover letter
Not verified
Assessment
Not verified
Deadline
Not stated

Where they hire

State eligibility is not yet verified.

About this role

Manager, Product Life Cycle Engineering Burlington, MA, US Overview Serve as a hands on Engineer responsible for development or revision of testing protocols and reports aimed at continued regulatory compliance with existing and revised industry standards related to Class I, II and III medical devices. Responsibilities Have management responsibilities over Product Life Cycle Engineers (Currently 2 direct reports). Have hands on development or revision responsibility of testing protocols and reports aimed at continued regulatory compliance with existing and revised industry standards related to Class I, II and III medical devices. Continuously engage with Regulatory Affairs and Quality affairs teams to ensure that all standards are current and fully applied to our products. Conduct Gap assessments on product technical documentation and make recommendations for improvement. Initiate change orders for implementation of changes or guide cross-functional groups to do the same. Participate in CAPA process as it relates to product conformance Develop strong partnerships with multi-functional leaders to ensure that alignment, efficiency, and execution meet business requirements Ensure that the voice of the customer is present in all decisions and that all design requirements are translated into practical design changes that can be verified and ultimately validated in manufacturing Ensure projects are carried out in compliance with regulatory requirements (GMP, ISO, MDD/MDR) & LeMaitre policy & procedure requirements Capture & disseminate knowledge acquired during projects to improve LeMaitre product development processes & systems Acquire resources from functional organizations, support groups & outside sources to ensure project success Provide assistance in related areas

Read the full description at careers-lemaitre.icims.com. FewerJobs shows a preview and links to the original posting.

Apply at careers-lemaitre.icims.com

Apply link not verified; last alive Jul 27, 2026.

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