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Robotic Medical Device Engineer Jobs (NOW HIRING)

Collabera

Medical device engineer

North Chicago, IL · On-site

... days, Medical, Dental and Vision insurance, 401K retirement savings plan, Life Insurance ... Evaluate and integrate relevant engineering advances for improving or solving problems Understand ...

iTech US, Inc.

Senior Medical Device Engineer

Blue Ash, OH · On-site

$96K - $131K/yr

Senior Medical Device Engineer PLM / Lifecycle Management Location: Blue Ash, OH Duration: 6+ Months Contract 7+ years of engineering experience in medical device or other regulated industries.

NAM Info Inc

Senior Medical Device Engineer

Blue Ash, OH · On-site

$96K - $131K/yr

Senior Medical Device Lifecycle Engineer Location: Blue Ash, OH Duration: 6 Months Contract We are seeking an experienced Senior Medical Device Lifecycle Engineer to lead product lifecycle and ...

Conflux Systems

Medical Device Test Engineer

Newton, MA · On-site

Develop and implement test methods for verification of complex medical robotic systems . * Execute ... Engineering . * 5+ years of experience in medical device testing , preferably with medical or ...

RXinsider LTD.

Medical Device Engineer 2

San Diego, CA · On-site

S. in Physics, Chemistry, Chemical Engineering, Materials Science and Engineering, Biomedical Engineering, Electrical Engineering, or a related discipline. * You have a technical background in ...

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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 10, 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.

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

Senior Medical Device Engineer

Fort Lauderdale, FL

ttg Talent Solutions
Recruiting and Staffing Services • 11 - 50 employees
Learn more about ttg Talent Solutionsexternal

$110K - $130K/yr (+ commission)

Full-time

Retirement, PTO

Posted 13 days ago

Job description

Senior Medical Device Engineer
Well-established U.S. pharmaceutical R&D - Global
Western Broward County - South Florida
Relocation assistance 
On-site | Full-time
 
ttg Talent Solutions is conducting a confidential search for a Senior Medical Device Engineer for a well-established U.S. pharmaceutical R&D center that is part of a global organization with a broad portfolio spanning generic, complex generic, and branded drug products. This hands-on role sits at the intersection of medical device engineering and pharmaceutical science, with a particular focus on inhalation and nasal drug-delivery systems, including dry powder inhalers (DPIs), metered-dose inhalers (MDIs), nasal sprays, and nebulizers.
Position Summary
The Senior Device Engineer will serve as the primary device and primary-packaging subject-matter expert within a cross-functional drug-product development organization, owning device development from early concept through commercial launch. The role requires technical depth, strong design-control and risk-management discipline, and the ability to challenge external partners, coach junior colleagues, and support regulatory interactions.
Key Responsibilities
Device Development and Engineering
  • Serve as the primary device and primary-packaging subject-matter expert across drug-product development programs from early concept through commercial launch.
  • Define and own product requirements for medical devices and drug-device combination products.
  • Recommend and defend strategies for material selection, design concepts, cost reduction, high-volume manufacturability, and process efficiency, supported by data.
  • Design, execute, interpret, and report device-development studies with emphasis on reliability testing, quality systems, and documentation rigor.
  • Develop robust devices and manufacturing and analytical processes for combination products, including injection-molded plastic components.
Design Controls, Risk, and Quality
  • Lead FMEA and FMECA risk-management activities and critically evaluate proposed technical solutions.
  • Lead and monitor Design Control documentation activities, including development of high-quality Design History Files (DHF).
  • Oversee human factors studies and related activities from planning through reporting.
  • Apply strong quality-system discipline and ensure development activities align with cGMP requirements and applicable ISO, ASTM, and ICH standards.
Cross-Functional, External, and Regulatory Leadership
  • Lead collaboration with internal teams and external development partners by setting expectations, monitoring progress against plan, and providing substantive technical challenge where needed.
  • Support Regulatory Affairs in preparing pre-registration submissions for medical devices and combination products and contribute to responses to Health Authority questions.
  • Lead or support direct interactions with regulatory bodies and relevant industry accreditation organizations.
  • Coach and develop team members and contribute meaningfully to project sub-teams, broader departmental strategy, and organizational goals.
Required Qualifications
  • Education: A relevant engineering degree at minimum (BSc or equivalent); an advanced degree in engineering or a scientific discipline (MSc or equivalent) is highly desirable.
  • Experience: At least five years in the medical device industry, with pharmaceutical development exposure strongly preferred. Hands-on experience with DPIs, MDIs, nasal sprays, and/or nebulizers is a meaningful differentiator.
  • Design and Manufacturing Depth: Demonstrated experience in product design, injection molding of plastic components, and equipment qualification. Proficiency with force-measurement and metrology tools. A background in electrical engineering or materials science is a plus.
  • Regulatory and Quality Fluency: Working knowledge of Design Control processes, cGMP requirements, and applicable ISO, ASTM, and ICH standards. Experience conducting FMEA, FMECA, and Human Factors Analysis.
  • Tools: Proficiency with SolidWorks, CAD platforms, and standard technical software environments used in medical device development.
  • Leadership: Proven ability to lead in a matrix organization by setting direction, building alignment, and developing people without relying on direct authority.
  • Communication: Strong written and verbal communication skills, including technical and scientific writing and the ability to present complex information clearly to cross-functional and regulatory audiences.
  • Work Location: Ability and willingness to work full-time on-site in the  Broward County  in South Florida. - easy access from Fort Lauderdale, Boca and Miami.  ( no state income tax ) 
Core Competencies
  • Cross-functional collaboration and stakeholder management.
  • Customer and patient centricity.
  • Developing talent and coaching others.
  • Innovation, creative problem-solving, and strategic agility in a regulated environment.
  • Process discipline, technical rigor, and result orientation.
Why This Opportunity
This is an opportunity to join a technically sophisticated R&D environment and lead device engineering across high-value drug-device combination products, with meaningful ownership from concept through commercialization and direct influence on product quality, manufacturability, regulatory readiness, and patient experience.
Compensation 
Base Salary: $110,000 – $130,000 per year (could be more for the right candidate) + full corporate benefits package, 401K, PTO and more .  Relocation assistance provided
Please apply on-line for immediate consideration. If you are match, you will be contacted by email, phone or text. Monitor your inbox, VM and spam for messages from the recruiter!!