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Founding Manufacturing Engineer – Medical Devices

Job in Los Angeles, Los Angeles County, California, 90079, USA
Listing for: Mydentalwig
Full Time position
Listed on 2026-07-31
Job specializations:
  • Engineering
    Manufacturing Engineer, Quality Engineering, Process Engineer
Salary/Wage Range or Industry Benchmark: 140000 - 190000 USD Yearly USD 140000.00 190000.00 YEAR
Job Description & How to Apply Below
Position: Founding Manufacturing Engineer – Medical Devices | MyDentalWig

MYDENTALWIG
Advanced Manufacturing. AI-Driven Healthcare. Preventive Innovation.

Building the future of intelligent manufacturing systems across healthcare, semiconductors, and AI infrastructure.

Employment Type: Full-Time

Reports To: Founder & CEO

Equity Eligible: Yes – Eligible to participate in the Company’s Equity Incentive Plan, subject to Board approval and applicable vesting provisions.

Compensation: $140,000–$190,000 annually, depending on qualifications and experience, plus benefits and equity participation.

About MYDENTALWIG

MYDENTALWIG is a privately capitalized advanced manufacturing company developing AI-integrated healthcare technologies as the first operational phase of Sainte Lydie City
, a long-term vision to build a vertically integrated industrial ecosystem in the United States valued at approximately $200 billion.

Our first platform,
AI²™ (Artificial Ingestive Intelligence), combines proprietary biosensing, artificial intelligence, and predictive metabolic modeling to help transform healthcare from reactive disease treatment to proactive disease prevention.

We are assembling a founding team of exceptional engineers and innovators to build technology that has never existed before.

About the Opportunity

This is not a traditional manufacturing engineering position.

As our Founding Manufacturing Engineer
, you will design the manufacturing processes that transform innovative prototypes into reliable, repeatable products.

Working closely with the Biomedical Engineer, Software Engineer, ML Engineer, FDA Regulatory Consultant, and Founder, you will establish MYDENTALWIG’s pilot manufacturing capability and lay the groundwork for future production scale-up.

This role combines engineering, process development, quality systems, equipment selection, supplier collaboration, and continuous improvement.

Primary Responsibilities
  • Design and implement pilot manufacturing processes for AI²™.
  • Develop assembly procedures, work instructions, and production documentation.
  • Collaborate with engineering teams to optimize products for manufacturability (Design for Manufacturing/Assembly).
  • Select, qualify, and support manufacturing equipment and tooling.
  • Assist with laboratory and pilot production facility layout.
  • Develop manufacturing workflows that support quality, efficiency, and traceability.
  • Work with suppliers to source components and evaluate manufacturing partners.
  • Establish production testing and inspection procedures.
  • Support process validation and continuous improvement activities.
  • Collaborate with the FDA Regulatory Consultant to ensure manufacturing processes align with applicable quality system requirements.
  • Assist in implementing inventory, material handling, and production planning systems.
  • Support pilot builds, engineering verification, and design validation activities.
  • Work closely with the Sales and Business Development teams to ensure manufacturing readiness aligns with commercialization objectives.
Preferred Technical Experience

Experience in several of the following:

  • Electronics assembly
  • Precision manufacturing
  • Lean Manufacturing
  • Six Sigma methodologies
  • Design for Manufacturing (DFM)
  • Design for Assembly (DFA)
  • Process validation
  • Root cause analysis
  • Failure Mode and Effects Analysis (FMEA)
  • Statistical Process Control (SPC)
  • CAD software (Solid Works, Fusion 360, Creo, or equivalent)
  • Manufacturing Execution Systems (MES)
  • ERP systems
  • Quality Management Systems (QMS)

Experience with sensor-based products, wearable technology, or regulated manufacturing environments is highly desirable.

Qualifications
  • Bachelor’s or Master’s degree in Manufacturing Engineering, Mechanical Engineering, Industrial Engineering, Biomedical Engineering, or a related field.
  • 5+ years of experience in manufacturing engineering or process development.
  • Experience transitioning products from prototype to production.
  • Strong understanding of manufacturing processes and quality systems.
  • Excellent problem-solving and analytical skills.
  • Strong communication and cross-functional collaboration abilities.
Preferred Qualifications
  • Experience with medical devices or healthcare technologies.
  • Experience in startup or high-growth environments.
  • Familiarity with FDA Quality System…
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