Manufacturing Engineer
Job in
Cambridge, Middlesex County, Massachusetts, 02140, USA
Listed on 2026-01-07
Listing for:
Nanobiosym
Full Time
position Listed on 2026-01-07
Job specializations:
-
Engineering
Manufacturing Engineer, Quality Engineering, Process Engineer -
Manufacturing / Production
Manufacturing Engineer, Quality Engineering
Job Description & How to Apply Below
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.
DUTIES- Coordinate a production and Engineering Team in a variety of manufacturing processes.
- Collaborate with team members and management to develop and improve injection molded and assembled products and processing thru numerous manufacturing steps.
- Develop and assist in the process and product monitoring, including the creation of a validation protocol (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 in a growing organization and an opportunity which will grow rapidly
- MS. or B.S. in Engineering (Plastics or Mechanical preferred) or equivalent experience
- Six Sigma Black Belt, a plus
- 2+ years of experience in molding, mold-making and tooling in manufacturing environment
- 2+ years of experience in diverse technical, materials, manufacturing and product design
- 2+ years expiernce with CAD
- Understanding of statistical analysis and statistical process control
- Electromechanical experience is required
- Recent experience with an FDA regulated (21 CFR 820) and/or ISO 13485 environment
- Good communication and organization skills
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