Senior Manufacturing Engineer — Lean, Validation & Strategy

Laborie Medical Technologies Corp; Maple Grove (MN); On-site; USD 140,000 - 190,000; Full time

Benefits offered by this job

Paid time off

Medical, Dental, Vision

Job summary

Laborie Medical Technologies Corp in Minnesota seeks a Principal Manufacturing Engineer to shape strategies across all Laborie sites, guiding operations, enhancements, and new product transfers. The role demands deep expertise in manufacturing, quality, and product development within a medical device context.

You will lead cross-functional initiatives, mentor engineers, and drive Lean improvements to reduce cycle times while ensuring ISO and regulatory compliance.

Qualifications

• 12+ years' experience as Manufacturing/Production Engineer (or 8+ with Master's)
• Bachelor's in Mechanical, Electrical, or Manufacturing Engineering required
• Experience in medical device industry preferred
• Knowledge of ISO 13485/ISO 9000 and safety regulations
• Proven ability to lead cross-functional projects and meet deadlines

Responsibilities

• Act as corporate SME, providing technical leadership and advising on new product development
• Lead high-impact, cross-functional projects with executive leadership alignment
• Drive manufacturing excellence by Lean initiatives to reduce cycle time and stabilize production
• Own design transfer and production readiness with cross-functional collaboration
• Lead validation and qualification activities (IQ, OQ, PQ, MSA)
• Improve product and process quality to meet regulatory requirements
• Provide data-driven insights via costs analysis, production planning, and forecasting

Skills

ERP systems (SAP)

SolidWorks

Microsoft Office

Lean Manufacturing

Design for Manufacturability (DFM)

Education

Bachelor's in Mechanical, Electrical, or Manufacturing Engineering

Tools

SAP

SolidWorks

Job description

Laborie Medical Technologies Corp in Minnesota seeks a Principal Manufacturing Engineer to shape strategies across all Laborie sites, guiding operations, enhancements, and new product transfers. The role demands deep expertise in manufacturing, quality, and product development within a medical device context.

You will lead cross-functional initiatives, mentor engineers, and drive Lean improvements to reduce cycle times while ensuring ISO and regulatory compliance.