Microscale Electromechanical Assembly Specialist

Job Description

Job DescriptionBuild Precision. Power Outcomes.

Join a team that transforms components into life-impacting medical devices. As a Microscale Electromechanical Assembly Specialist, you’ll assemble, test, and document with cleanroom discipline and craftsmanship.

Status: Contract-to-Perm
Schedules: 1st, 2nd, and 3rd Shift

Why this role matters

• Your precision ensures device performance and patient safety.
• Your documentation keeps products compliant and traceable.
• Your problem-solving drives continuous improvement across lines.

Core responsibilities

• Uphold cleanroom standards through proper gowning and environmental protocols.
• Assemble plastic and metal parts into finished medical products following approved SOPs and work instructions.
• Use tools and equipment: manual/powered hand tools, manual presses, assembly fixtures, calibrated gauges, measurement instruments, microscopes, and test fixtures.
• Execute to documentation: BOMs, product flow charts, work orders, check sheets, visual aids, production reports, and assembly drawings.
• Perform processes such as soldering, crimping, mechanical fastening, sealing, ultrasonic welding, bonding, and adhesive application (Epoxy, RTV).
• Complete kitting using parts lists, barcode scanners, and inventory software.
• Carry out start-up and end-of-day equipment checks and verifications.
• Conduct in-process inspections; escalate quality or operational nonconformances promptly.
• Maintain a safe, orderly station; participate in safety training and report hazards.
• Engage in cross-functional Kaizen/continuous improvement activities.
• Achieve quality, throughput, and GMP targets aligned with customer and Regulatory Affairs requirements; read and apply product-specific operating procedures after training.
• Flag any deviation from process sheets immediately; maintain rigorous attention to detail.
• Collaborate with Engineers and line leads to resolve issues and optimize procedures.
• Record quality data, WIP status, test results, labor/timecards, and special project notes accurately.
• Comply with company policies, manufacturing procedures, and applicable ISO, QSR, and FDA regulations.

Qualifications

• 2+ years of hands-on manufacturing experience.
• Experience assembling, testing, and documenting mechanical and electrical devices.
• Clear, professional communication skills—written and verbal.
• Resilient, flexible, and ready to tackle unexpected tasks.
• Preferred: background in medical device manufacturing.
• Preferred: familiarity with medical device regulatory procedures, lean manufacturing, and production processes.
• Strong manual dexterity, excellent hand–eye coordination; adept with small parts under a microscope.
• Comfort using tweezers, torque drivers, magnifiers, and microscopes.

Impact starts at the bench

Bring your craftsmanship and compliance mindset—we’ll provide the platform to make a measurable difference.