Manufacturing Engineer

Halma plc

$90K — $120K *
Manufacturing & Automotive
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • B.S. in Manufacturing, Mechanical, or Industrial Engineering or equivalent experience.
  • 3-5 years of experience in medical device or hardware manufacturing supporting production environments.
  • Experience designing tools and fixtures for assembly and production.
  • Proven track record of troubleshooting real-time production issues, including non-conformances and bottlenecks.
  • Certified SolidWorks Associate or equivalent experience of at least 3 years.
  • Proficient with inspection tools and methods.
  • Strong understanding of FDA regulations and design change processes.

Responsibilities

  • Revise product designs for enhancements or new lines.
  • Design and improve tools and fixtures for testing and inspection.
  • Troubleshoot and analyze root causes of failures.
  • Document maintenance protocols for new equipment.
  • Create and maintain production procedures throughout the product lifecycle.
  • Establish verification and validation protocols for processes.
  • Lead quality improvement initiatives in production processes.
  • Develop automated methods for data collection and reporting.
  • Conduct training for assemblers and technicians on equipment operations.
  • Support product failure analysis for customer complaints.
  • Perform design change documentation and analysis.
  • Engage in workflow efficiency studies for waste reduction.

Benefits

  • Medical, dental, vision, life, and disability insurance.
  • 401(k) retirement plan.
  • Flexible spending and health savings accounts.
  • Paid holidays and paid time off.
  • Parental leave and employee assistance program.
Full Job Description
Job Title: Manufacturing Engineer

Company: MicroSurgical Technology
Location: On-siteRedmond, WA
Department: Manufacturing Engineering
Reports To: Sr. Manufacturing Engineering Manager

Job Summary:

Design and improve manufacturing production processes, including material selection, machine operations, automation and quality control, with a strong emphasis on supporting and optimizing day-to-day production line performance.

Key Responsibilities
  • Revise existing product designs for improvement or new line extensions.
  • Design new and revise existing tools and fixtures for assembly, test, and inspection
  • Troubleshoot and conduct failure root cause analysis.
  • Develop and document IQ, OQ, PQ and maintenance protocols for new equipment and fixtures.
  • Develop and maintain production assembly, test, and inspection procedures through product life cycle.
  • Develop verification and validation protocols for equipment and processes, including validation of cleaning, packaging, and sterilization.
  • Participate in Material Review Board (MRB) to evaluate and disposition discrepant material, conduct failure root cause analysis, develop rework and repair methods, identify and document corrective and preventative action.
  • Develop automated data collection and reporting methods.
  • Lead production process quality improvement.
  • Determine training and certification requirements for assemblers and technicians for production processes and equipmen.t
  • Provide product failure analysis support for customer complaints and returns.
  • Perform workflow design, yield improvement, waste reduction, time and motion efficiency studies.
  • Create engineering design and process change orders with required documentation, technical justification/change effects analysis, and impact to operations.
  • Create, document, and conduct training and certifications for fixture/equipment operation, and critical methods.
  • Perform other duties as assigned.


Qualifications:
  • B.S. in Manufacturing, Mechanical, or Industrial Engineering or equivalent experience.
  • 3-5 years of experience in medical device or hardware manufacturing, with direct support of production manufacturing environments.
  • Experience designing tools and fixtures for assembly, test and production.
  • Experience responding to real-time production issues (non-conformances, downtime, bottlenecks) and implementing corrective actions.
  • Certified SolidWorks Associate or 3+ years of equivalent experience.
  • Proficiency with inspection tools (micrometers, calipers, optical comparators) and methods.
  • Experience troubleshooting mechanical devices and performing root cause analysis.
  • Solid understanding of design change requirements and processes in FDA regulated manufacturing environment.
  • Ability to perform Gage R & R Analysis for equipment qualifications.


Pay Range: $90K-$120K per year. Compensation is determined based on job-related knowledge, skills, experience, education, certifications, internal equity, and market conditions. This position may also be eligible for a discretionary annual bonus and/or other incentive compensation.

This position is eligible for a benefits package that includes medical, dental, vision, life, and disability insurance; 401(k) retirement plan; flexible spending and health savings accounts; paid holidays; paid time off; parental leave; employee assistance program; and other company benefits.

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