Job Description

Step Into the Cleanroom and Build What Matters

As a Cleanroom Medical Device Assembly Technician, you’ll own the end-to-end build of precision medical products—assembling, testing, and documenting electro-mechanical components with accuracy and care.

Employment type: Contract-to-Perm

Shifts available: 1st, 2nd, and 3rd

A day in the life

You suit up, enter a controlled environment, and move efficiently between stations. You follow approved procedures to assemble plastic and metal components, verify quality under a microscope, and record results as you go. Throughout the day, you collaborate with line leads and engineers to troubleshoot, contribute ideas to continuous improvement, and wrap up with end-of-day equipment checks so the next shift starts strong.

What you’ll do

• Protect cleanroom integrity by wearing proper garments and following all environmental controls.
• Assemble plastic and metal parts into finished medical devices per approved manufacturing procedures.
• Operate and handle small hand tools (manual and powered), manual presses, assembly fixtures, calibrated instruments, measurement devices, microscopes, and test fixtures.
• Follow and complete documentation such as BOMs, product flow charts, work orders, check sheets, visual aids, production reports, and assembly drawings.
• Perform operations such as soldering, crimping, mechanical assembly, sealing, ultrasonic welding, bonding, and adhesive work (including Epoxy and RTV) as needed.
• Kit assemblies using a parts list, scanner, and inventory software.
• Conduct routine start-up and end-of-day equipment inspections or verifications.
• Inspect work in-process; promptly escalate quality or operational issues to the appropriate leader.
• Keep your station organized and hazard-free; participate in safety programs, meetings, and training, and raise any safety concerns.
• Contribute to cross-functional continuous improvement initiatives.
• Meet quality, throughput, and Good Manufacturing Practice expectations to satisfy customer and Regulatory Affairs requirements; understand operating procedures for products you’re trained on.
• Maintain sharp attention to detail; report anything that deviates from approved process sheets immediately.
• Partner with Engineers and line leads to resolve issues and refine procedures for quality and efficiency.
• Accurately document quality checks, WIP status, test results, labor/timecards, and special projects.
• Follow general safety rules, manufacturing procedures, company policies, and comply with ISO, QSR, and FDA regulations.

What you’ll bring

• At least 2 years of hands-on experience in a manufacturing environment.
• Proven capability in assembly, testing, and documentation of mechanical and electrical devices.
• Strong interpersonal, verbal, and written communication skills.
• Adaptability and willingness to take on varied tasks in a dynamic setting.
• Preferred: prior medical device manufacturing experience.
• Preferred: working knowledge of medical device regulatory procedures, lean manufacturing, and production processes.
• Excellent hand–eye coordination and manual dexterity; comfortable with small parts assembly under a microscope.
• Proficiency with tweezers, torque drivers, magnifiers, and microscopes.

If you’re meticulous, safety-minded, and motivated by building devices that help people, you’ll thrive here.

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