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Manufacturing Technician

Job in Canton, Norfolk County, Massachusetts, 02021, USA
Listing for: Cambridge Recruiters
Full Time position
Listed on 2026-06-19
Job specializations:
  • Manufacturing / Production
    Manufacturing Production, Manufacturing Engineer, Medical Device Industry, Quality Engineering
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

30-person commercial-stage medical device startup seeking a hands‑on Manufacturing Technician to support the production, testing, and assembly of our innovative gastrointestinal implant and delivery system. This individual will play a critical role in building medical devices, supporting manufacturing process development, troubleshooting production issues, and helping scale operations as the company continues commercial growth.

The ideal candidate enjoys working in a fast‑paced startup environment, takes pride in producing high‑quality products, and is comfortable working closely with Manufacturing, Engineering, and Quality teams.

Responsibilities
  • Perform assembly, inspection, testing, packaging, and labeling of medical device components and finished products according to approved procedures and work instructions.
  • Support manufacturing operations for both implantable devices and catheter/delivery system products.
  • Maintain accurate production records, Device History Records (DHRs), travelers, and associated manufacturing documentation.
  • Operate and maintain production equipment, fixtures, tools, and test systems.
  • Assist Manufacturing Engineers with process development, validation activities, and continuous improvement initiatives.
  • Identify, troubleshoot, and communicate manufacturing issues, non‑conformances, and equipment problems.
  • Ensure compliance with FDA Quality System Regulations, ISO 13485 requirements, and company quality procedures.
  • Assist with inventory management, material handling, and production scheduling activities as needed.
  • Support manufacturing scale‑up efforts as production volumes increase.
Required Qualifications
  • 4 - 6+ years of experience in medical device, life sciences, or other regulated manufacturing environments.
  • Medical device manufacturing experience.
  • Experience working in an ISO 13485 and/or FDA‑regulated environment.
  • Strong mechanical aptitude and experience using hand tools, fixtures, and manufacturing equipment.
  • Ability to read and follow detailed work instructions, drawings, and assembly procedures.
  • Experience documenting work accurately and maintaining production records.
  • Strong attention to detail and commitment to quality.
  • Comfortable working in a team‑oriented startup environment.
  • Ability to stand for extended periods and perform repetitive assembly tasks.
Preferred Qualifications
  • Experience with catheter assembly, implantable devices, or precision mechanical assemblies.
  • Familiarity with cleanroom manufacturing practices.
  • Experience supporting IQ/OQ/PQ validations and process verification activities.
  • Basic understanding of GMP, Design Controls, and manufacturing documentation requirements.
  • Soldering, adhesive bonding, crimping, laser marking, or similar precision assembly skills.
Key Attributes
  • Hands‑on and mechanically inclined.
  • Detail‑oriented with strong quality focus.
  • Self‑motivated and dependable.
  • Able to work effectively in a growing startup environment.
  • Strong English communication and teamwork skills.
  • Eager to learn new processes and technologies.

Local Candidates only

Must Have US Work Authorization, no VISA sponsor ships

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