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Manufacturing Engineer

Job in Sunnyvale, Santa Clara County, California, 94086, USA
Listing for: Intuitive
Full Time position
Listed on 2026-09-03
Job specializations:
  • Engineering
    Manufacturing Engineer, Quality Engineering, Process Engineer, Mechanical Engineer
  • Manufacturing / Production
    Manufacturing Engineer, Quality Engineering
Job Description & How to Apply Below

Manufacturing Engineer

This entry level manufacturing engineer will support multiple manufacturing lines for both mature and new instruments and accessories for the Ion platform. This engineer must be able to support existing manufacturing lines, recommend and implement improved manufacturing processes, and lead manufacturing line transfers. The role requires the ability to collaborate effectively across functions ranging from Quality and Design to Manufacturing in the US and Mexico.

Essential Job Duties

  • Lead manufacturing line transfer projects, including:
    • Lead project management effectively, including monitoring schedules for multiple functions across two plants
    • Procure, assemble, and qualify custom mechanical and electromechanical equipment
    • Improve equipment documentation and design as needed for continuous improvement in preparation for further transfers
    • Develop an in-depth understanding of our manufacturing processes, and transfer knowledge to new engineers and assemblers from a remote location to facilitate an effective transfer
    • Troubleshoot electromechanical equipment problems, including collaboration with third party equipment makers as needed, e.g. braiders, laminators, or testing equipment
  • Support several Ion manufacturing lines including:
    • Establish regular communication with the production team to ensure they have the best support possible for both short and long term needs
    • Manage product reliability improvements from concept to implementation
    • Identify, design, qualify, document and introduce assembly/test fixtures and equipment
    • Improve process flows of Ion instrument manufacturing lines to optimize for reliability, efficiency, capacity, cost, and technician safety
    • Execute and mentor others in manufacturing process validations, process FMEAs, and other elements associated with production Master Validation Plans
    • Provide product and process Design for Manufacturing/Assembly (DFX) input to enhance manufacturability, and lead improvement implementations
    • Manage manufacturing strategy and production capability for Ion Instrument lines to minimize customer backorders
    • Maintain compliance with medical device quality system including corrective action closure, discrepant material disposition and Engineering Change Order (ECO) implementation
    • Provide technical support for failure analyses and root cause investigations of product failures
  • Contribute to the establishment of group and individual objectives consistent with overall product development goals, including priority setting, establishment of metrics, and effectively communicating progress
  • Provide resource budget estimates for product and process improvements, tooling development, and testing
  • Works with Quality and Regulatory to ensure that the team follows appropriate GMP, design history file (DHF), and device history record (DHR) guidelines per FDA requirements

Qualifications

Required Skills and Experience

  • Strong technical problem solving and analytical skills
  • Familiar with various component manufacturing processes (machining, injection molding & MIM, stamping, coining, extrusion)
  • Familiar with mechanical CAD software (Solid Works)
  • Familiar with Process and Equipment Qualifications (IQ/OQ/PQ/PPQ)
  • Strong organizational skills and ability to work on several fast-paced projects simultaneously
  • Mechanical design and analysis skills, including statics, dynamics, kinematics, strength of materials, and stress analysis is a plus
  • Able to communicate effectively and professionally with cross-functional peers, executive leadership, internal customers, and external suppliers
  • Prior experience with Design Control processes for medical devices and/or clinical applications of the surgical instruments, and/or automated equipment design is a plus
  • 25% travel (including international) is required

Required Education and Training

  • B.S. degree in engineering discipline, with 5 years of experience in the manufacturing engineering space. Or M.S. in engineering discipline, with 3 years of experience in the manufacturing engineering space.

Additional Information

  • Due to the nature of our business and the role, please note that Intuitive and/or your customer(s) may require that you show current…
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