About The Position

InnoTECH Staffing is partnering with a cutting-edge neurostimulation startup in Boston that is developing next-generation implantable technology designed to make a real difference for patients. This is a rare opportunity to join early, work side-by-side with leadership, and directly shape a Class III active implantable device from prototype through commercialization. The role is a Senior Manufacturing Engineer. Must be able to work onsite in Boston and be able to travel to CM partners. This isn’t a maintenance manufacturing job. You’ll be at the center of innovation—owning how a complex, miniaturized implantable lead is actually built, scaled, and perfected. You’ll work hands-on at the bench, in close collaboration with R&D, and directly with the CTO to bring a breakthrough device to life.

Requirements

  • B.S. or M.S. in Mechanical, Materials, or related engineering field
  • 2–5+ years of medtech manufacturing experience
  • Hands-on experience with miniature implantable assemblies , including at least two of the following: Polymer overmolding / insert molding around fine wires, Multi-lumen extrusion handling, Centerless grinding, Laser welding of fine-gauge components, Polyurethane reflow
  • Working knowledge of FDA Design Controls (21 CFR 820.30) and ISO 13485

Nice To Haves

  • Experience with Class III implantable devices (neuro, cardiac, cochlear, etc.)
  • Micro-scale manufacturing or micro-injection molding
  • Advanced failure analysis (cross-sectioning, metallography, micro-CT/X-ray)
  • Knowledge of implantable materials and ISO 10993
  • Startup or early-stage company experience

Responsibilities

  • Own manufacturing process development and qualification from early builds through commercialization
  • Embed with contract manufacturers during critical builds to dial in processes in real time
  • Lead root-cause investigations on device failures (bench, aging, in vivo)—including cross-sectioning and failure analysis
  • Design and execute DOEs to characterize and optimize new processes
  • Develop and author pFMEAs, validation protocols (IQ/OQ/PQ), process specs, and change orders
  • Collaborate cross-functionally with R&D and suppliers to improve manufacturability and robustness
  • Establish the Manufacturing Quality Plan for a next-gen implantable lead

Benefits

  • Full medical, dental, and vision coverage
  • Generous PTO + company holidays
  • Paid parental leave
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