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Injection Molding Engineer

United States, Cambridge · Job Posted March 20, 2026
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Job Description

Nanobiosym is on the cusp of rewriting the rules of personalized medicine, novel technologies, and healthcare delivery. Founded by a renowned MIT and Harvard trained Physician and Physicist, Nanobiosym's innovative pipeline of products leverage novel advances in physics, biomedicine, and nanotechnology. Awarded the first ever X-PRIZE for healthcare, and a recipient of multiple other prestigious peer-reviewed funding awards, Nanobiosym is currently adding to its talented team as it expands into a global commercial enterprise. We are currently seeking Engineering candidates to add to our growing team.

Job Responsibility

  • Collaborate with team members and management to develop and improve injection molded and assembled products and processing thru numerous manufacturing steps
  • Develop and implement validation protocols (IQ/OQ/PQ) that comply with FDA regulations
  • Provide troubleshooting focus and direction for the team with details of root cause analysis
  • Utilizes Lean principles to develop creative, thorough and practical technical solutions
  • This is a hands-on position where the requirement is to wear many hats where opportunities grow rapidly
  • Utilize Lean principles to develop creative, thorough and practical technical solutions
  • Responsible for debugging, packaging and sterilization
  • Document changes to processes and equipment using change management system
  • Participate in cross functional teams to improve safety, quality, efficiency and overall productivity
  • Monitor and validate existing injection molding processes and molds to develop and execute continuous improvement opportunities
  • Identify risks, technical options value propositions, and champion solutions

Requirements

  • M.S. or B.S. in Engineering (Plastics or Mechanical preferred)
  • Six Sigma Black Belt is preferred
  • 7+ years of experience in molding, micromolding, mold flow, mold-making and tooling in manufacturing environment
  • Experience in design improvements and solid works/CAD
  • 7+ years of experience in diverse technical, materials, manufacturing and product design
  • Experience in statistical analysis and statistical process control
  • Recent experience with medical device development, in an FDA regulated (21 CFR 820) and/or ISO 13485 environment
  • Strong written and verbal communication skills as well as documentation and organizational skills
  • Strong mechanical aptitude
  • A passion for problem solving and thrive on handling multiple priorities and working in a fast-paced environment

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