Med-Device Manufacturing Engineer: Process Improvement & DFM

Domico Med Device LLC; Mundy Charter Township (MI); On-site; USD 85,000 - 110,000; Full time

Job summary

Domico Med-Device LLC is seeking a Manufacturing Engineer in Fenton, MI. The role focuses on driving continuous improvement, manufacturing process development, and design for manufacturability.

You will collaborate with cross‑functional teams to resolve production issues and ensure compliance with QMS, FDA 21 CFR Part 820, and ISO 13485. The ideal candidate has a mechanical/industrial engineering background, experience with SolidWorks, and strong communication and problem‑solving skills.

Qualifications

• Bachelor’s degree in mechanical or industrial engineering or equivalent.
• Experience with SolidWorks or equivalent.
• Proficiency in Microsoft Word and Excel.
• Strong communication skills and able to interface with multiple departments.
• Focus on quality work and results orientation.
• Team player with ability to collaborate across disciplines.
• Proficient in problem solving and analytical thinking.
• Effective time management and workload organization.

Responsibilities

• Drive continuous improvement to increase efficiency and reduce scrap.
• Coordinate cross‑functional activities to support manufacturing.
• Assist in design for manufacturability and PFMEA risk reviews.
• Develop and document manufacturing processes and work instructions.
• Collaborate on DFMEA, process capability, and qualification activities.
• Provide production floor support and mentor operators.

Skills

SolidWorks

MS Word

MS Excel

Problem solving

Analytical thinking

Time management

Team player

Communication skills

Education

Bachelor’s degree in mechanical or industrial engineering

Tools

ERP systems

Global Shop

Technical writing

Job description

Domico Med-Device LLC is seeking a Manufacturing Engineer in Fenton, MI. The role focuses on driving continuous improvement, manufacturing process development, and design for manufacturability.

You will collaborate with cross‑functional teams to resolve production issues and ensure compliance with QMS, FDA 21 CFR Part 820, and ISO 13485. The ideal candidate has a mechanical/industrial engineering background, experience with SolidWorks, and strong communication and problem‑solving skills.