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Manufacturing Engineer

  • Redmond, WA, United States

$92,000 to $112,000 USD / year

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Job details

Pay
$92,000 to $112,000 USD / year
Experience
5+ years of hands-on manufacturing, test, or process engineering experience in a high-reliability hardware environment.
Posting language
English
Posted

Original job description

About the Role

We are seeking a hands-on Manufacturing Engineer to own the assembly, test, and continuous improvement of our ultrasound probe cell. In this on-site role, you will be the technical authority on the probe production floor, bridging R&D (mechanical, electrical, and software engineering) and factory operations.

You will define, document, and optimize processes for complex electromechanical medical devices across both sustaining production and new product introduction (NPI). If you are a strong root-cause problem solver who is comfortable with a soldering iron, an oscilloscope, and a technician's questions on the line, we want to hear from you.

Key Responsibilities

Process Engineering & Floor Support

  • Probe Cell Ownership: Own probe assembly and test processes for both sustaining production and NPI builds.
  • Assembly Line Engagement: Work directly alongside assembly technicians and operators to resolve daily technical issues, train on new processes, and streamline workflows.
  • Process Optimization: Design, implement, and continuously improve assembly procedures, fixtures, tooling, test equipment, and cell layout to maximize yield, quality, and throughput.
  • Special Builds: Build and rework engineering and test assemblies to support NPI, validation, and design engineering activities.

Troubleshooting & Failure Analysis

  • Root Cause Analysis: Lead structured root cause investigations (e.g., 5 Whys, Fishbone, 8D, fault tree) on production failures and drive effective, verified corrective actions.
  • Electrical Debug: Diagnose complex electromechanical failures at the component, sub-assembly, and system levels using schematics, multimeters, oscilloscopes, and other test equipment.
  • Failure Analysis: Perform failure analysis on production rejects and customer returns, including teardown and cable dissection to isolate failure locations, in support of Service and Engineering.

Test & Production Systems

  • Production Test: Support and troubleshoot production test systems, including acoustic output testing and reference data collection, in line with applicable standards.
  • Production Software & Tools: Partner with software and electrical engineering to improve production software tools, test automation, and the transfer of new tools into production.
  • Validation: Support equipment, process, and test method validation (IQ/OQ/PQ) and verification activities.

Continuous Improvement

  • Data-Driven Focus: Analyze yield, defect, and NCR trend data to prioritize improvement efforts.
  • Statistical Methods: Apply DOE and SPC to characterize, control, and improve processes.
  • Cost & Capability: Identify, justify (ROI), and implement new fabrication or test methods and equipment that improve capability and reduce unit cost.

Documentation & Compliance

  • Work Instructions: Author, edit, and maintain clear, visual Assembly Instructions (AIs), test and rework instructions, and Manufacturing Process Specifications (MPS) for mechanical housings, cabling, acoustic transducers, and PCB integration.
  • DFM / DFT: Participate in NPI design reviews, advocating for Design for Manufacturability, Assembly, and Testability with design engineers and suppliers.
  • Change Management: Prepare and manage Engineering Change Orders (ECOs), BOMs, and deviations in PLM to transfer designs and process changes into production.
  • Quality & Regulatory: Maintain compliance with FDA QMSR (21 CFR Part 820), ISO 13485, and internal quality standards. Support NCRs and Corrective/Preventive Actions (CAPA).

Qualifications

Qualifications & Skill Requirements

Education & Experience (one of the following)

  • Bachelor's degree in Mechanical, Electrical, Manufacturing, or Biomedical Engineering (or a related discipline) plus 3+ years of manufacturing, test, or process engineering experience; or
  • 5+ years of hands-on manufacturing, test, or process engineering experience in a high-reliability hardware environment.

Required Skills

  • Root Cause Analysis: Demonstrated track record of solving complex production problems with structured RCA methods and verifying the fix.
  • Electrical Debug & Soldering: Strong hands-on electrical troubleshooting skills, including reading schematics and using a multimeter and oscilloscope; proficient in fine-pitch soldering and rework of PCBAs, wire harnesses, and cables.
  • Electromechanical Fundamentals: Working knowledge of electrical systems (PCBAs, harnesses, sensors, power distribution) and mechanical assemblies (precision tolerances, enclosure fit, structural hardware).
  • Lean & Quality Tools: Experience applying Lean Manufacturing (5S, Kaizen, Value Stream Mapping, Kanban), pFMEA, DOE, and SPC.
  • Data Analysis: Advanced Excel skills and comfort with statistical software for analyzing yield and defect data.
  • Regulated Environment: Experience in an ISO 13485 / FDA-regulated medical device environment is highly preferred; experience with other regulated or high-reliability electromechanical products will be considered.

Preferred Skills (a Plus)

  • Python Scripting: Ability to write or modify Python scripts for test automation, data collection, or analysis.
  • Linux / Ubuntu: Familiarity with Ubuntu or other Linux environments, including the command line, as used on production test stations.
  • 3D CAD: Proficiency in SolidWorks, Creo, or similar for designing fixtures and jigs and creating visual assembly illustrations.
  • Ultrasound Knowledge: Experience with transducer/probe assembly, acoustic shielding, coaxial cabling, high-frequency signal integrity, or acoustic output testing.
  • Mobile Platforms: Familiarity with Android or iOS devices and applications used in production or test.
  • PLM Systems: Experience managing change orders and BOMs in a Product Lifecycle Management system.
  • Certifications: IPC J-STD-001 or IPC-A-610 certification.

Soft Skills & Working Style

  • Excellent written and verbal communication, with a proven ability to write crisp, unambiguous visual work instructions.
  • High emotional intelligence and the interpersonal skills to build trust with assembly technicians, quality engineers, and R&D designers.
  • Ability to prioritize and manage multiple assignments while maintaining a high level of quality.
More about this job

Skills

  • Assembly
  • Process improvement
  • Medical devices
  • Process engineering
  • Troubleshooting
  • Root cause analysis
  • Troubleshoot
  • Industrial software
  • Electrical engineering
  • Test automation
  • SPC
  • Improve business processes
  • Documentation
  • Regulatory compliance
  • Manufacturing processes
  • MPS
  • Printed circuit boards
  • DFT
  • Change management
  • PLM
  • Transfer designs
  • Biomedical engineering
  • Troubleshooting electrical systems
  • Wire harnesses
  • Lean manufacturing
  • Kanban
  • Data analysis
  • Microsoft Excel
  • Python
  • Linux
  • Ubuntu
  • Dassault Systemes SolidWorks
  • PTC Creo
  • Communication skills
  • Interpersonal skills

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