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Medical Device Engineer - Product Development & Manufacturing

Job in Township of Hampshire, Kane County, Illinois, USA
Listing for: Trident Manufacturing, Inc
Full Time position
Listed on 2026-10-14
Job specializations:
  • Engineering
    Manufacturing Engineer, Quality Engineering, Mechanical Engineer, Product Engineer
  • Manufacturing / Production
    Manufacturing Engineer, Quality Engineering, Product Engineer
Salary/Wage Range or Industry Benchmark: 60000 - 90000 USD Yearly USD 60000.00 90000.00 YEAR
Job Description & How to Apply Below
Location: Township of Hampshire

Medical Device Engineer - Product Development & Manufacturing

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Trident is seeking a skilled Engineer to join our rapidly growing team. As a contract manufacturer of medical devices, we collaborate with startups, leading OEMs, and top-tier component manufacturers to develop innovative manufacturing processes, bringing medical devices to market and enhancing healthcare outcomes. Our expertise in medical device manufacturing, combined with our automotive heritage and continuous improvement mindset, positions us uniquely to help our customers reduce costs and manufacturing risks before design freeze and prepare for successful routine production.

This role offers an excellent opportunity for a technically proficient engineer eager to gain diverse experience in medical device product development and manufacturing. We value candidates who can apply their technical skills and contribute directly to our engineering efforts.



Note:

This is a 100% on-site position in Pingree Grove, IL, with minimal travel. Only local candidates will be considered.

Responsibilities
  • Collaborate with customers and internal teams to design, develop, and manufacture medical devices from concept through production launch.
  • Review customer requirements and design specifications, providing feedback on design for manufacturing to reduce costs and complexity while improving manufacturability.
  • Review product designs for manufacturability, provide detailed DFM feedback, and design custom assembly fixtures and simple automation solutions.
  • Work closely with Quality Engineering to establish and document quality control measures, including test methods and process validation (IQ/OQ/PQ).
  • Engage with suppliers to ensure high-quality components and processes, from initial quotation through PPAP approval and ramp-up.
  • Develop and maintain process documentation, including manufacturing instructions and validation studies.
  • Participate in quality improvement initiatives and cost-saving projects post-launch.
  • Provide technical support and troubleshooting for manufacturing processes and equipment.
  • Qualifications
    • Bachelor's degree in Mechanical Engineering or related field.
    • 1-4 years of experience in design, development, or manufacturing of mechanical products or equipment, preferably in medical devices.
    • Strong problem-solving skills with a hands-on engineering approach.
    • Proficiency in Solid Works or similar CAD software for product and fixture design.
    • Effective communication of complex technical concepts, both verbally and in writing.
    • Experience managing detailed technical documentation.
    • Knowledge of manufacturing processes such as injection molding, die cutting, metal forming, machining, sterile packaging, thermoforming, ultrasonic welding, and UV curing adhesives.
    Seniority level

    Entry level

    Employment type

    Full-time

    Job function

    Quality Assurance

    Industries

    Medical Device

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