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Intern Medical Device Engineer Jobs (NOW HIRING)

Intel

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 ...

GlaxoSmithKline

Device Engineer

Zebulon, NC

Experience with design controls, risk management and quality processes used in medical device ... Master's degree in engineering or related field and additional device development experience.

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 ...

Intel

Device Engineer

Hillsboro, OR · On-site

$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 ...

kindeva

Senior Device Engineer

Maryland Heights, MO

$101K - $138K/yr

Experience in Medical Device or Combination Products Design Controls, Production, Sustaining Engineering role or related field * B.S. Degree in Engineering discipline with 7 - 9 years experience * M.

Intel Corporation

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 ...

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 ...

Gilead

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 ...

kindeva

Senior Device Engineer

Maryland Heights, MO

$101K - $138K/yr

Experience in Medical Device or Combination Products Design Controls, Production, Sustaining Engineering role or related field * B.S. Degree in Engineering discipline with 7 - 9 years experience * M.

kindeva

Senior Device Engineer

Maryland Heights, MO

$101K - $138K/yr

Experience in Medical Device or Combination Products Design Controls, Production, Sustaining Engineering role or related field * B.S. Degree in Engineering discipline with 7 - 9 years experience * M.

kindeva

Senior Device Engineer

Maryland Heights, MO · On-site

$101K - $138K/yr

Experience in Medical Device or Combination Products Design Controls, Production, Sustaining Engineering role or related field * B.S. Degree in Engineering discipline with 7 - 9 years experience * M.

nLIGHT

Device Engineer

Vancouver, WA

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 ...

Kellton Tech

Medical Device Assembler

Madison, WI · On-site

$23 - $24/hr

Job Title: Medical Device Assembler Location: Madison, WI (Onsite) Pay Rate: $23-24/hr on W2 ... Engineering group as required. Working Conditions: Clean, temperature controlled environment.

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All JobsIntern Medical Device Engineer Jobs

Intern Medical Device Engineer information

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How much do intern medical device engineer jobs pay per hour?

As of Jul 17, 2026, the average hourly pay for intern medical device engineer in the United States is $19.31, according to ZipRecruiter salary data. Most workers in this role earn between $16.11 and $20.91 per hour, depending on experience, location, and employer.

What is the difference between Intern Medical Device Engineer vs Junior Medical Device Engineer?

AspectIntern Medical Device EngineerJunior Medical Device Engineer
CredentialsTypically pursuing or recently completed a relevant degreeBachelor's or Master's in biomedical, mechanical, or related engineering
Work EnvironmentInternship setting, supervised, learning-focusedEntry-level professional role, more independent tasks
Employer & Industry UsageMedical device companies, research labs, internshipsMedical device companies, manufacturing, R&D teams

Intern Medical Device Engineers are usually students or recent graduates gaining hands-on experience, while Junior Medical Device Engineers are entry-level professionals with some work experience. The internship focuses on learning and support, whereas the junior role involves more responsibility in product development and testing.

What types of projects and responsibilities can an Intern Medical Device Engineer expect to be involved with during their internship?

As an Intern Medical Device Engineer, you can expect to participate in hands-on projects such as assisting in prototype development, performing laboratory testing, and collecting and analyzing data for product improvement. You'll often work closely with senior engineers, quality assurance teams, and regulatory specialists to ensure devices meet safety and compliance standards. Interns may also help prepare technical documentation and contribute to brainstorming sessions for new product features, providing a well-rounded exposure to the medical device development process. This collaborative environment offers valuable experience and networking opportunities for future career growth.

What does an Intern Medical Device Engineer do?

An Intern Medical Device Engineer assists in the design, development, and testing of medical devices under the supervision of experienced engineers. Their responsibilities may include conducting research, creating prototypes, analyzing data, and ensuring products meet regulatory standards. Interns often collaborate with cross-functional teams and gain hands-on experience in the medical device industry. This role provides valuable exposure to engineering processes and helps interns build skills required for a future career in biomedical engineering.

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

To thrive as an Intern Medical Device Engineer, you need a solid background in biomedical engineering or a related field, along with foundational knowledge of device design and regulatory standards. Familiarity with CAD software, prototyping tools, and basic laboratory testing equipment is typically required, and coursework or certification in medical device regulations can be advantageous. Strong problem-solving, teamwork, and communication skills help interns contribute effectively to multidisciplinary projects and adapt to feedback. These competencies are crucial for ensuring safe, innovative device development and successful collaboration in a regulated industry.
What cities are hiring for Intern Medical Device Engineer jobs? Cities with the most Intern 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 Intern Medical Device Engineer jobs? States with the most job openings for Intern Medical Device Engineer jobs include:
Intern Medical Device Engineer jobs near you
Senior Device Engineer - Electromechanical Combination Products (Lifecycle Management, Design Contro

Senior Device Engineer - Electromechanical Combination Products (Lifecycle Management, Design Contro

3 Key Consulting

Thousand Oaks, CA

$44 - $48/hr

Full-time

Re-posted 17 days ago

Job description

Job Title: Senior Device Engineer – Electromechanical Combination Products (Lifecycle Management, Design Control, CAPA) - (JP15488)
Location: Thousand Oaks, CA. 91320
Employment Type: Contract
Business Unit: Electromechanical Platform
Duration: 1+ year with likely extensions and/or conversion to permanent
Posting Date: 06/15/2026
Pay Rate: $44 - $48/hour W2 with benefits
Notes: 3-5 days onsite depending on business needs - Standard hours - Local Candidates Only.
3 Key Consulting is hiring an Senior Device Engineer – Electromechanical Combination Products (Lifecycle Management, Design Control, CAPA) for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
Ideal candidate: Seeking candidates with experience in combination products, electromechanical systems, or medical devices, a background in pharma, and hands-on expertise in design control and testing.
Our client is seeking a contract electromechanical combination product Device Engineer. The Device Engineer will participate in design development and lifecycle management-related activities for commercialized drug delivery devices and devices under development.
Why is the Position Open?
Supplement additional workload on team
Top Must Have Skills:
  • Lifecycle Management Experience with electromechanical platforms
  • Root Cause Analysis and Technical Problem Solving
  • Proven success in cross-functional engagement and being a team player
  • Nice to have: Early device development experience

Day to Day Responsibilities:
  • Provide ongoing lifecycle management (LCM) support for electromechanical combination products, including post-market activities, design improvements, and cross-functional issue resolution to ensure product reliability and compliance.
  • Lead complaint investigations by performing detailed failure analysis, identifying root causes, and developing data-driven action plans in collaboration with quality, manufacturing, and regulatory teams.
  • Drive and manage quality system processes including CAPAs, deviations, and change controls, ensuring timely closure, robust documentation, and alignment with regulatory and internal requirements.
  • Collaborate closely with external suppliers to support LCM activities, including issue resolution, component updates, root cause analysis, CAPAs and continuous improvement initiatives to maintain supply continuity and product performance.
  • Manage change assessments driven by internal and external changes during the life cycle of the combination product
  • Participate in and support cross-functional design reviews for combination product development.
  • Provide design verification support for combination products, ensuring compliance with Quality System Requirements, Design Control (21 CFR 820.30), and ISO 13485.
  • Lead and execute on-site testing and verification activities for electromechanical delivery systems and related platforms.
  • Develop, review, and execute test protocols, reports, and technical documentation in accordance with design control and regulatory expectations.
  • Perform data verification, analysis, and traceability reviews to ensure product performance meets user needs and design inputs.
  • Partner cross-functionally with R&D, Human Factors, Quality, Regulatory, and Manufacturing teams to drive design robustness, risk mitigation, and design transfer readiness.

Basic Qualifications:
  • Doctorate degree OR Masters degree and 2 years of experience OR Bachelors degree and 4 years of experience OR Associates degree and 8 years of experience OR High school diploma / GED and 10 years of experience

Preferred Qualifications:
    • Master’s or Bachelor’s Degree in Engineering Discipline (Mechanical, Biomedical, Electrical) with 3-5 years (or 2 years with Masters) of professional experience in highly regulated environment (strong preference for medical device, biopharma and/or combination product experience).
    • Experience with electromechanical systems, injection devices, medical devices or delivery platforms preferred.
    • Demonstrated expertise in lifecycle management, data analysis, and protocol/report generation under design control.
    • Strong understanding of materials coordination, supplier interaction, and lab testing logistics.
    • Proven ability to work in cross-functional project teams, communicate technical results clearly, and lead execution to meet program milestones.
    • Working proficiency in statistical analysis software (Minitab)
    • Smartsheets proficiency is a plus.
    • Ability to work independently and dynamically across functional teams
    • Excellent written and verbal communication skills
    • Must be capable of working on multiple projects in a deadline driven environment.
    • The position is designed for candidates at a mid-career stage, with scope and responsibilities aligned to that level of experience.

Red Flags:
  • Unable to be consistently on-site in Thousand Oaks
  • Low motivation/engagement at prospect of working with medical device and/or combination products
  • Poor written and verbal communication
  • Candidates looking to be in a management role. Too much experience 10+ YOE.

Interview process:
  • 1:1 with hiring manager
  • 1:2 or 1:3 with prospective team members
  • Remote video Interviews

We invite qualified candidates to send your resume to resumes@3keyconsulting.com.  If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.