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Full Time Medical Device Engineer Jobs (NOW HIRING)

Device Engineer

Phoenix, AZ · On-site

$72K - $93K/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 ...

Device Engineer

Hillsboro, OR

$79K - $102K/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 ...

Device Engineer

Santa Clara, CA

$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 ...

Device Engineer

Phoenix, AZ

$72K - $93K/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 ...

Device Engineer III

Foster City, CA · On-site

$117K - $152K/yr

We are seeking a highly skilled and proactive Device Engineer III to support testing, method ... Experience in combination product development , medical device testing, or pharmaceutical/biotech ...

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 ...

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 ...

**Job Title: **Med-Device Assembler (x2) **Pay Rate: **$21-$23/hr. ($21/hr. without soldering $23/hr ... Collaborate with Manufacturing Engineering to support lean manufacturing processes **Qualifications:

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Medical Device Assembler

Milpitas, CA · On-site

$25 - $27/hr

We are seeking a Medical Device Assembler to support the build and integration of capital medical ... Read and interpret assembly drawings; use computers for basic programming, menu navigation, and ...

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 ...

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Full Time Medical Device Engineer information

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$21

$49

$96

How much do full time medical device engineer jobs pay per hour?

As of Jun 21, 2026, the average hourly pay for full time 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 is the difference between Full Time Medical Device Engineer vs Medical Device Quality Engineer?

AspectFull Time Medical Device EngineerMedical Device Quality Engineer
Required CredentialsBachelor's in Engineering, certifications like CQA or Six Sigma beneficialBachelor's in Engineering or Life Sciences, certifications like CQE or ISO auditor
Work EnvironmentDesign labs, R&D departments, manufacturing facilitiesQuality assurance labs, compliance departments, manufacturing sites
Employer & Industry UsageMedical device companies, biotech firms, healthcare device manufacturersMedical device companies, regulatory agencies, compliance firms
Common Search & ComparisonYesYes

Full Time Medical Device Engineers focus on designing, developing, and testing medical devices, working closely with R&D teams. Medical Device Quality Engineers concentrate on ensuring products meet quality standards and regulatory requirements. Both roles are essential in the medical device industry but differ in their primary responsibilities and work environments.

More about Full Time Medical Device Engineer jobs
What cities are hiring for Full Time Medical Device Engineer jobs? Cities with the most Full Time 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 Full Time Medical Device Engineer jobs? States with the most job openings for Full Time Medical Device Engineer jobs include:
Infographic showing various Full Time Medical Device Engineer job openings in the United States as of June 2026, with employment types broken down into 74% Full Time, 25% Part Time, and 1% Contract. Highlights an 87% Physical, 5% Hybrid, and 8% Remote job distribution, with an average salary of $103,662 per year, or $49.8 per hour.
Senior Device Engineer, Pharmaceutical R&D

Senior Device Engineer, Pharmaceutical R&D

Transpire BIO Inc.

Weston, FL

$99K - $136K/yr

Full-time

Posted 8 days ago


Job description

Position Summary

The Senior Device Engineer is responsible for device engineering activities in the context of pharmaceutical research and development (R&D). The device mechanical engineer will be responsible for early to late-stage device development activities and commercialization of drug-device combination products. The Device engineer will be responsible for design, prototyping, technical analysis, and testing of orally inhaled and nasal drug products (OINDPs). Provide device engineering leadership in the direction, initiation, planning, coordination, implementation, execution, control, and completion of specific device project(s) ensuring consistency with organizational strategy, commitments, and goals. The device engineer will need to ensure that the device designs meet user needs, regulatory and quality requirements, and consider manufacturability. This is a hands-on position which requires daily tactical responsibilities leading up to strategic decisions.

Essential Duties and Responsibilities

  • In support of the Product Development Teams, provide technical leadership in the device development area.
  • Execute design and development of orally inhaled and nasal drug products (OINDPs) following design controls.
  • Lead and execute analysis for device and product characterization, design feasibility, and design verification.
  • Lead and execute technical analyses including statistical analysis and tolerance analysis.
  • Lead root cause investigations.
  • Support scale-up and commercialization efforts.
  • Document studies and author documents per US FDA, EMA, MHRA and other global health authority requirements.
  • Interface and lead activities with third party contract research, development, and manufacturing organizations.
  • Contribute towards and maintain device design history files (DHF).
  • Document standard operating procedures (SOPs) for design controls in the context of pharmaceutical drug-device combination products.
  • Provide project updates/reporting through program governance.
  • Provide leadership and support for inter-site best practices (technology transfer, process validation, etc.) and phase appropriate guidelines and policies.
  • Execute project strategy, priorities, and milestones ensuring visibility and accountability.
  • Proactively lead with integrity and engage cross functional project teams and stakeholders.
  • Support organizational / departmental initiatives.
  • Prepare and conduct presentations to all levels of the organization which may include project technical and budgetary information.

Required Qualifications

  • A M.S, in Mechanical Engineering, Electrical Engineering, Material Sciences or related discipline with 7 to 10 years, B.S. with 10 to 14 years device development experience in pharmaceutical or related field.
  • Experience with device development in the context of pharmaceutical R&D and product development is a must to have.
  • Must possess expert knowledge of mechanical design with preference for SolidWorks.
  • Must possess expert knowledge of tools to conduct statistical and tolerance analysis.
  • Must possess knowledge of manufacturing processes including injection molding and metal machining processes.
  • Must possess knowledge of regulations and standards including US 21 CFR Part 820, ISO 13485, ISO 14971, ISO 10993, EU MDR etc.
  • Experience with device assembly processes including manual, semi-automated and/or commercial scale automated processes is a plus.
  • Experience in development of orally inhaled and nasal drug products (OINDPs) is a plus.
  • Experience in mold tool design, optimization and qualification is a plus to have.
  • Experience with Notified Bodies and CE marking is a plus.
  • Strong English language skills including writing ability and oral communication.
  • Demonstrates good judgment as well as cultural, social, and environmental awareness.

Preferred Qualifications

  • Experience in a regulated laboratory (pharma, biotech, medical device, mechanical, or environmental)
  • Knowledge of GMP, GLP, or ISO standards

Why Join Us?

We are a fast-growing pharmaceutical startup dedicated to innovation and improving patient outcomes. Join us to gain hands-on experience in a growing pharmaceutical business, get exposure to various functions with opportunities for career development and work in a collaborative and supportive work environment.