Manufacturing Engineer, Medical Devices & Process

Marmon Holdings, Inc.; Charlottesville (VA); On-site; USD 75,000 - 110,000; Full time

Benefits offered by this job

Competitive compensation

401K with company match

Medical/Dental/Vision

Vacation & Paid Holidays

Company-wide Marmon initiatives

Job summary

MicroAire, part of Marmon Holdings, Inc., seeks a Manufacturing Engineer to support sustaining products and design transfers in a regulated medical-device environment. You will lead process development, fixture/tooling design, validation, and continuous improvement, serving as a bridge across design, manufacturing, quality, and suppliers.

You will contribute to design transfer activities, process validation, and manufacturing documentation while collaborating with cross‑functional teams to

Qualifications

• Bachelor’s degree in Mechanical, Manufacturing, or Biomedical Engineering.
• Experience in manufacturing engineering within medical devices or regulated industries (open to new grads with internship experience).
• Experience with design control, process validation, and manufacturing documentation.

Responsibilities

• Design, develop, and optimize manufacturing processes, fixtures, tooling, and equipment.
• Support Design Transfer from development through production.
• Participate and/or lead design and manufacturing change control activities.
• Troubleshoot production issues using root cause and failure analysis.
• Support process validation, equipment qualification, and regulatory compliance.
• Collaborate with Quality, Supply Chain, Operations, and suppliers on improvements.
• Lead DFM/DFA activities to ensure efficient, high-quality manufacturing.

Skills

Problem solving

Communication

Collaboration

Education

Mechanical Engineering

Manufacturing Engineering

Biomedical Engineering

Tools

Design Controls

Process Documentation

Job description

MicroAire, part of Marmon Holdings, Inc., seeks a Manufacturing Engineer to support sustaining products and design transfers in a regulated medical-device environment. You will lead process development, fixture/tooling design, validation, and continuous improvement, serving as a bridge across design, manufacturing, quality, and suppliers.

You will contribute to design transfer activities, process validation, and manufacturing documentation while collaborating with cross‑functional teams to