Principal Manufacturing Engineer
$145,000–$155,000 year
On-siteSalt Lake City, Utah, United States or Plymouth, Minnesota, United States
Job Summary
Act as corporate SME, providing technical leadership, guiding operational strategy, and advising on new product development and design changes. Lead high-impact, cross-functional projects, partnering with executive leadership to align manufacturing initiatives with business objectives and growth strategies, including acquisition evaluations. Drive manufacturing excellence and efficiency by optimizing workflows, conducting time studies, improving line layouts, implementing Lean initiatives to reduce cycle time and stabilize production. Own design transfer and production readiness, collaborating cross-functionally to implement new products and updates while training and mentoring technicians and engineering teams. Lead validation and qualification activities (IQ, OQ, PQ, MSA) ensuring compliance with ISO standards and robust process capability. Improve product and process quality by defining testing methods, establishing standards, and ensuring manufacturing processes meet regulatory and performance requirements. Provide data-driven insights through costs analysis, production planning, and reporting, including labor/material forecasting and performance trend analysis. 25% travel required.
Required Qualifications
- 12+ years' experience as Manufacturing/Production Engineer (or 8+ with Master's)
- Bachelor's in Mechanical, Electrical, or Manufacturing Engineering
- Proven expertise in manufacturing operations, quality, and product development, including Design for Manufacturability (DFM) principles
- Hands-on experience with ERP systems (SAP preferred)
- Hands-on experience with SolidWorks
- Hands-on experience with Microsoft Office tools
- Strong background in Lean Manufacturing methodologies and continuous improvement practices
- Demonstrated ability to lead projects, meet tight deadlines, and collaborate effectively with cross-functional teams
- Working knowledge of ISO 13485/ISO 9000 standards
- Working knowledge of health & safety regulations
- Strong organizational/time management skills
- Ability to travel 25%
Desired Qualifications
- Medical device industry experience
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