ZipRecruiter

Log In

1

Medical Device Engineer Jobs (NOW HIRING)

nLIGHT

Device Engineer

Vancouver, WA

$103K - $130K/yr

Device Engineer II: $90,000 - $115,000 * Senior Device Engineer: $103,000 to $130,000 Other ... Medical, Dental and Vision Benefits, including prescription and orthodontia with employee-paid ...

nLIGHT

Device Engineer

Vancouver, WA · On-site

$103K - $130K/yr

Device Engineer II: $90,000 - $115,000 * Senior Device Engineer: $103,000 to $130,000 Other ... Medical, Dental and Vision Benefits, including prescription and orthodontia with employee-paid ...

Intel

Senior Foundry Device Engineer

Phoenix, AZ

$103K - $142K/yr

We provide benefits that promote a healthy, enjoyable life: excellent medical plans, wellness ... CMOS device engineering and device physics, and at least 1 of the following areas: logic ...

Murata Americas

Staff Device Engineer

San Mateo, CA · On-site

$260K/yr

Provide mentorship and technical guidance to engineers working on device modeling, characterization ... Comprehensive benefits package including medical, dental, and vision insurance. * Generous Paid ...

Power Integrations

Staff Device Engineer

Branchburg, NJ

$133K - $200K/yr

Staff Device Engineer Responsibilities * Design and qualify high-voltage GaN power devices ... medical benefits, ESPP, 401K, tuition reimbursement and time off programs. For additional benefits ...

Murata America

Staff Device Engineer

San Mateo, CA

$260K/yr

Provide mentorship and technical guidance to engineers working on device modeling, characterization ... Comprehensive benefits package including medical, dental, and vision insurance. * Generous Paid ...

Power Integrations

Staff Device Engineer

San Jose, CA · On-site

Staff Device Engineer Responsibilities * Design and qualify high-voltage GaN power devices ... medical benefits, ESPP, 401K, tuition reimbursement and time off programs. For additional benefits ...

Power Integrations

Staff Device Engineer

San Jose, CA

$133K - $200K/yr

Staff Device Engineer Responsibilities * Design and qualify high-voltage GaN power devices ... medical benefits, ESPP, 401K, tuition reimbursement and time off programs.For additional benefits ...

Power Integrations

Staff Device Engineer

Branchburg, NJ · On-site

$133K - $200K/yr

Staff Device Engineer Responsibilities * Design and qualify high-voltage GaN power devices ... medical benefits, ESPP, 401K, tuition reimbursement and time off programs.For additional benefits ...

next page

Showing results 1-20

All JobsMedical Device Engineer Jobs

Medical Device Engineer information

See salary details

$21

$49

$96

How much do medical device engineer jobs pay per hour?

As of Jun 8, 2026, the average hourly pay for medical device engineer in the United States is $49.84, according to ZipRecruiter salary data. Most workers in this role earn between $35.10 and $59.62 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Medical Device Engineer, and why are they important?

To thrive as a Medical Device Engineer, you need a solid background in biomedical, mechanical, or electrical engineering, often supported by a relevant bachelor's or master's degree. Familiarity with CAD software, regulatory standards (such as FDA or ISO 13485), and design validation tools is typically required. Strong problem-solving, communication, and teamwork skills are essential for collaborating on multidisciplinary projects and ensuring product safety. These competencies are crucial for developing innovative, compliant devices that improve patient outcomes and meet rigorous industry standards.

What does a Medical Device Engineer do?

A Medical Device Engineer is responsible for designing, developing, testing, and improving medical devices used in healthcare settings. They work closely with doctors, scientists, and regulatory bodies to ensure that devices are safe, effective, and compliant with industry standards. Their work includes creating prototypes, conducting risk assessments, and overseeing the manufacturing process. Medical Device Engineers play a crucial role in bringing innovative technologies to market that help diagnose, treat, or monitor medical conditions.

What are some common challenges Medical Device Engineers face when bringing a new product from concept to market?

Medical Device Engineers often encounter challenges such as navigating complex regulatory requirements, ensuring product safety and efficacy, and coordinating with cross-functional teams including design, manufacturing, and quality assurance. Balancing innovation with compliance, managing timelines, and addressing unforeseen technical issues are also typical hurdles. Successful engineers leverage strong project management and communication skills to collaborate effectively and bring devices to market efficiently.

What is the difference between Medical Device Engineer vs Biomedical Engineer?

AspectMedical Device EngineerBiomedical Engineer
CredentialsBachelor's or Master's in Engineering, certifications in medical device designBachelor's or Master's in Biomedical Engineering or related field
Work EnvironmentDesign, develop, test medical devices in labs or manufacturing settingsResearch, develop medical equipment, or work in clinical settings
Industry UsagePrimarily in medical device manufacturing companiesHospitals, research institutions, medical device companies

Medical Device Engineers focus on designing and testing specific medical devices, ensuring compliance and safety. Biomedical Engineers have a broader scope, working on medical equipment, implants, and research. Both roles require similar credentials and often overlap in industry settings, but their primary focus differs.

What Does a Medical Device Engineer Do?

A medical device engineer is an engineering professional who develops new medical equipment and medical devices. As a medical device engineer, your work will vary depending on your area of expertise and may include biomedical research, material research and sourcing, computer-aided design work, and teaming up with doctors and patients. You also must understand the manufacturing process and ensure the products you design are both useful and cost-effective. You look for innovative solutions to medical problems and design new equipment diagnoses and treatments.

More about Medical Device Engineer jobs
What cities are hiring for Medical Device Engineer jobs? Cities with the most Medical Device Engineer job openings:
What are the most commonly searched types of Medical Device Engineer jobs? The most popular types of Medical Device Engineer jobs are:
What states have the most Medical Device Engineer jobs? States with the most job openings for Medical Device Engineer jobs include:
What job categories do people searching Medical Device Engineer jobs look for? The top searched job categories for Medical Device Engineer jobs are:
What are popular job titles related to Medical Device Engineer jobs? For Medical Device Engineer jobs, the most frequently searched job titles are:
Medical Device Engineer jobs near you
Principal Device Development Engineer - CONTRACT

Principal Device Development Engineer - CONTRACT

Ocular Therapeutix

Bedford, MA • On-site

Full-time

Posted yesterday

Job description

Ocular Therapeutix, Inc. (NASDAQ:OCUL) is a biopharmaceutical company focused on the formulation, development, and commercialization of innovative therapies for diseases and conditions of the eye using its proprietary bioresorbable hydrogel-based formulation technology, ELUTYX™. Ocular Therapeutix has built a robust product pipeline of drug delivery solutions developed to reduce the complexity and burden of the current standard of care and position itself to become a leader in the ophthalmic space.
Outside of the ophthalmic realm and behind the doors of our headquarters in Bedford, MA, we strive to build a strong culture where employees can flourish and achieve their career goals. We encourage out of the box thinking, cross-functional collaboration, and creativity.
Position Summary:
The Principal Medical Device Engineer is a highly experienced and strategic leader in coordinating the ideation, assessment, and development of drug delivery technologies and medical devices. This role focuses on long-term technical vision, innovation, and team leadership while also remaining hands-on with complex technical challenges. The engineer is responsible for managing projects, ensuring compliance, and contributing to the overall success of the company's medical device portfolio.
Principal Duties and Responsibilities include the following:
  • Leads the design and development of new or improved medical devices, ensuring they meet regulatory requirements, quality standards, and user needs.
  • Ensure high-quality science, technology, and deliverables while ensuring compliance with global regulatory and quality requirements to support development and lifecycle management of Ocular drug delivery systems.
  • Oversees design verification testing and validation of prototypes and final products to ensure safety, effectiveness, and performance.
  • Operates with a high degree of autonomy to lead and conduct research and development activities to invent/improve drug delivery systems, with direct input to strategic decision-making.
  • Mentors and guides junior engineers, providing technical direction and support.
  • Manages project timelines, budgets, and resources to ensure timely and cost-effective delivery of medical devices.
  • Research device clinical use, standards, and other relevant regulatory guidance documents to support new product development and regulatory submissions with compliance to governing procedures, 21CFR 820.30 Design Control, CFR Part 4 Combination Products, and ISO 14971 Risk Management for medical devices and/or combination products.
  • Assist in writing IND/NDA regulatory responses as needed.
  • Identifies and explores new technologies and materials for medical device development.
  • Collaborates with various teams, including manufacturing, marketing, and other product stakeholders to develop design requirements and ensure product success.
  • Identifies and resolves technical issues, ensuring product quality and performance.
  • Analyzes data from testing, research, and manufacturing processes to identify trends and areas for improvement.
  • Develops and implements change management plans for existing products, ensuring compliance and minimizing disruption.
  • Partner with other functions, including Manufacturing, Safety/Clinical, Human Factors, Quality, Regulatory, and Design Engineering, to lead and perform risk assessments.

Qualification Requirements:
  • Bachelor's or Master's degree in Mechanical Engineering, Biomedical Engineering or a related field.
  • 15+ years of experience in medical device design, development, and testing.
  • 5+ years of experience with combination product development (injectable or ophthalmic products preferred).
  • Experience with all phases of product development from initial concept through commercialization.
  • Experience in third party management (manufacturers, labs, and consultants)
  • Experience creating, maintaining, and remediating Design History Files (DHFs) and ensuring compliance with regulatory requirements for parenteral combination products is preferred (21 CFR parts 4 & 820, ISO 13485, 14971 & IEC 62366).
  • Experience mentoring and guiding junior engineers; leading other engineering disciplines to execute and overcome product development technical challenges.
  • Experience with Project Management, Gantt Charts, (PMP certification a plus).
  • Experience with CAD software, drafting standards, materials science, and tolerance analysis.
  • Prior experience with generating human factors deliverables to comply with IEC 62366 and FDA Human Factor guidance.
  • Strong communication, leadership, problem-solving, and collaboration skills are essential.
  • Experience developing and implementing new testing methods for medical devices to ensure safety and effectiveness. Experience conducting Measurement System Analysis.
  • Experience performing a risk assessment on a new medical device and developing mitigation strategies. Knowledge of ISO 14971 and FMEA standards. Experience conducting user risk assessments.
  • Experience with statistical techniques used in product development as well as manufacturing. Six Sigma Greenbelt or equivalent a plus.

Hourly Pay
$88-$95 USD
Ocular Therapeutix is an Equal Opportunity Employer and complies with all applicable federal, state, and local laws regarding nondiscrimination. Ocular Therapeutix provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, or status as a veteran. For information on how Ocular Therapeutix collects, stores, and utilizes candidate information please see our privacy policy found at https://www.ocutx.com/privacy-policy/. For the Privacy Notice for California Job Applicants, please see CCPA Applicant Notice.

Apply