Engineer: Injection Molding Engineer

Injection Molding Engineer

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 leverages advances in physics, biomedicine, and nanotechnology. Awarded the first ever X-PRIZE for healthcare, and a recipient of multiple prestigious peer-reviewed funding awards, Nanobiosym is expanding its talented team into a global enterprise.

We are currently seeking Engineering candidates to join our growing team.

DUTIES

• Collaborate with team members and management to develop and improve injection molded and assembled products and processes through various manufacturing steps.
• Develop and implement validation protocols (IQ/OQ/PQ) compliant with FDA regulations.
• Provide troubleshooting guidance with root cause analysis.
• Utilize Lean principles to develop creative, thorough, and practical technical solutions.
• This is a hands-on position requiring versatility and rapid growth opportunities.
• Responsible for debugging, packaging, and sterilization processes.
• Document process and equipment changes using the change management system.
• Participate in cross-functional teams to improve safety, quality, efficiency, and productivity.
• Monitor and validate existing injection molding processes and molds, and develop continuous improvement initiatives.
• Identify risks, evaluate technical options, and champion solutions.

QUALIFICATIONS

• S. or B.S. in Engineering (Plastics or Mechanical preferred).
• Six Sigma Black Belt certification is preferred.
• 7+ years of experience in molding, micromolding, mold flow, mold-making, and tooling in a manufacturing environment.
• Experience in design improvements and proficiency with Solid Works/CAD.
• 7+ years of diverse technical experience in materials, manufacturing, and product design.
• Experience in statistical analysis and process control.
• Recent experience with medical device development in FDA (21 CFR 820) and/or ISO 13485 regulated environments.
• Strong written and verbal communication skills, along with documentation and organizational abilities.
• Strong mechanical aptitude.
• A passion for problem-solving and ability to handle multiple priorities in a fast-paced environment.