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Robotic Medical Device Engineer Jobs (NOW HIRING)

Cresilon

$77K - $105K/yr

The Senior Medical Device R&D Engineer is responsible for leading the design and development activities of new products and improving existing products in compliance with all quality and regulatory ...

Intel

Device Engineer

Santa Clara, CA · On-site

$85K - $110K/yr

You will work closely with a team of engineers to push the boundaries of device performance, power ... Candidates should never be required to pay recruitment fees, medical examination fees, or any other ...

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Robotic Medical Device Engineer information

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$29K

$105.6K

$169K

How much do robotic medical device engineer jobs pay per year?

As of Sep 12, 2026, the average yearly pay for robotic medical device engineer in the United States is $105,605.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,500.00 and $127,000.00 per year, depending on experience, location, and employer.

What are popular job titles related to Robotic Medical Device Engineer jobs?

For Robotic Medical Device Engineer jobs, the most frequently searched job titles are:

Sr Staff Device Engineer

Lexington, MA • On-site

Scorpion Therapeutics
51 - 200 employees
Learn more about Scorpion Therapeuticsexternal

Other

Posted 14 days ago

Job description

Sr. Staff Device Engineer (Commercial Device Engineering - CDE)Responsibilities:
  • Serve as device SME for combination product device lifecycle management for on-market products.
  • Lead change controls, manufacturing process validation, device product complaint handling, and regular review of DHF.
  • Support post-market surveillance and provide input to MDR and post-market surveillance reports.
  • Act as commercial device technical lead with cross-functional teams to manage lifecycle of commercial combination products.
  • Conduct technical investigations; analyze manufacturing and commercial expansion technical aspects.
  • Oversee commercial device qualification; coordinate tech transfer (verification/validation) for new drug delivery devices; solve technical issues.
  • Lead gap assessments/remediation and guide risk management activities; lead projects within budget.
  • Manage design control activities: specifications, design verification/validation, design transfer, test protocols/reports.
  • Support manufacturing expansion and process validation; ensure quality regulation system alignment (DHF, MDR, ISO13485, ISO14971).
Minimum Qualifications:
  • PhD (3+ yrs), MS (5+ yrs), or BS (8+ yrs) in Mechanical/Electrical/Biomedical Engineering or related.
  • SME in medical devices, especially drug delivery systems (e.g., PFS, pen injectors, autoinjectors, needle safety devices) with technical leadership.
  • Knowledge of design controls and quality system requirements; cGMP and combination product guidance.
  • Strong understanding of manufacturing/process and packaging; experience drafting technical content; author URS, protocols, reports, and assessments.
  • Experience with technology transfer and test method development/validation; technical leadership in cross-functional settings.
  • Experience with medical device LCM change controls, complaint investigations, and post-market surveillance.
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