Manufacturing Engineer Intern, Implant

Capstan Medical, Inc.Santa Cruz, CA
Onsite

About The Position

The Manufacturing Engineering Intern will support the development and optimization of scalable manufacturing processes for heart valve production. This role provides hands-on exposure to implant manufacturing in a fast-paced structural heart medical device startup. The intern will work closely with Manufacturing Engineering, R&D, Quality, and Operations teams to support process improvements, documentation activities, and new product introduction efforts.

Requirements

  • Currently pursuing a Bachelor’s or Master’s degree in Mechanical Engineering, Biomedical Engineering, Manufacturing Engineering, or related engineering field
  • Interest in medical devices, implantable technologies, or regulated manufacturing environments
  • Ability to work independently while taking direction from experienced engineers
  • Strong organizational skills and attention to detail
  • Process Development & Optimization – Ability to design, document, and refine scalable manufacturing processes for medical devices.
  • CAD & Engineering Tools – Experience in tools like SolidWorks or AutoCAD for fixture/tooling design.
  • Root Cause Analysis – Resourceful and proactive in identifying, analyzing, and resolving manufacturing issues.
  • Fixture & Equipment Design – Ability to design and troubleshoot jigs, fixtures, and semi automated equipment.
  • Document Control – Ability to work within a QMS and manage engineering change orders

Nice To Haves

  • Junior, Senior, or Graduate student preferred
  • Assembly Techniques – Familiarity with precision assembly or laboratory techniques is helpful

Responsibilities

  • Support development and improvement of manufacturing processes for heart valve components and assemblies.
  • Help collect and analyze manufacturing data to support yield, throughput, and continuous improvement initiatives.
  • Participate in root cause investigations and help implement corrective and preventive actions.
  • Draft and update work instructions, process documentation, and engineering change records under supervision.
  • Assist with fixture, tooling, or simple equipment design using CAD tools.
  • Support equipment qualification and process characterization activities.
  • Observe and help facilitate operator training activities for new processes or equipment.
  • Contribute to cleanroom manufacturing support tasks and documentation readiness for audits.
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