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Intern Medical Device Engineer Jobs (NOW HIRING)

AngioSafe

Medical Device R&D Engineer

San Jose, CA · On-site

$115K - $175K/yr

Bachelor's degree in Mechanical Engineering or related engineering discipline preferred * Minimum 5 years of medical device R&D experience * Hands-on catheter prototyping and testing experience ...

Dexcom

Sr Medical Device Engineer

San Diego, CA · On-site

$110K - $152K/yr

Cpk, ANOVA, T-Test, MSA, GR&R, DOE You will work with vendors & diverse engineering teams to onboard new equipment and processes. You develop requirements and specifications for new equipment and ...

Dexcom, Inc.

Sr Medical Device Engineer

San Diego, CA · On-site

$110K - $152K/yr

Cpk, ANOVA, T-Test, MSA, GR&R, DOE You will work with vendors & diverse engineering teams to onboard new equipment and processes. You develop requirements and specifications for new equipment and ...

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 ...

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 ...

Intel

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 ...

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 ...

Gilead Sciences, Inc.

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 ...

Gilead

Device Engineer III

Foster City, CA

$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.

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 ...

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.

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

As of Jun 5, 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 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 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 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 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
Research and Development Senior Medical Device Engineer

Research and Development Senior Medical Device Engineer

Cresilon, Inc.

Brooklyn, NY • On-site

$109K - $150K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 24 days ago

Job description

Cresilon® is a Brooklyn-based biotechnology company that develops, manufactures, and markets hemostatic medical devices utilizing the company's proprietary hydrogel technology. The company's plant-based technology has revolutionized the current standard by stopping traumatic and surgical bleeds in seconds without the need for extended manual pressure. The company's current and future product lines target veterinary, human trauma, and human surgical applications. Cresilon's mission is to save lives. Learn more about the company at www.cresilon.com.
Description:
The Senior Medical Device Engineer is responsible for leading the design and development activities of new products and improving existing products in compliance with all quality and regulatory requirements. They will be responsible for authoring technical documents for the development of medical devices and combination products according to relevant Design Control regulations and standards. The person in this position will also be responsible for providing project-specific support, including technical analysis and review of supplier documentation as required. The position has a scientific focus that includes formulation development, product performance characterization, and implementation, including prototype design and fabrication, and data generation through designed experiments.
The Senior Medical Device Engineer is expected to aspire for excellence with a bias toward action, willing to roll up their sleeves, get hands-on, and do what's necessary to move projects forward in a fast-paced environment. They are committed to designing and developing products that dominate the marketplace and improve healthcare by partnering with our customers to drive purposeful innovation, resulting in best-in-class products. The Medical Device Engineer will work with a multidisciplinary team of researchers. This is a multi-faceted job in a highly collaborative environment across multiple functions that will require flexibility as well as an ability to learn about and develop new technologies and explore new techniques in pursuit of product innovation and robustness.
Role level is contingent on experience, but this is not an entry level role.. This is a full-time, on-site position, located in Brooklyn, New York.
Responsibilities
  • Create and lead experimentation for exploratory and/or product development research focusing on polymeric materials devices and their use.
  • Define new product functional requirements (design inputs/user needs) and evaluate the design's overall effectiveness, cost, reliability, and safety.
  • Lead cross-functional teams to develop new products, address design issues, and maintain existing designs.
  • Apply strong problem-solving skills to find solutions to complex problems.
  • Work independently to plan and schedule own activities necessary to meet project timelines.
  • Work cooperatively with, quality, manufacturing, regulatory, clinical, and marketing to ensure project success.
  • Lead the creation of design history file documentation through the new product development process.
  • Develop new implant and instrument designs utilizing Solidworks and modeling/detail design specifications.
  • Generate technical protocols/reports to support device safety and efficacy.
  • Invent/create concepts and designs and submit invention disclosures.
  • Ensure that all design activities adhere to FDA Quality System Regulations and ISO 13485 design control and risk management requirements. Lead material/design/process changes through a design control process, with well-documented research/analyses.
  • Author protocols and reports including development studies and design verification/validation activities.
  • Develop and execute test methods to aid in exploratory research, product development, and quality control; conduct chemical and mechanical property evaluation tests to assess the desirability of process or formulation changes.
  • Exercise technical judgment in the design, execution, and interpretation of experiments within the scope of project responsibilities and ensure the use of professional concepts to solve complex problems in creative and effective ways, in conformance with scientific methods and procedures.
  • Prepare samples as required for testing, or other evaluations and data analysis, including in voice-of-customer (VOC) labs.
  • Interface with customers, suppliers, and internal cross-functional team members to develop specifications and coordinate prototype fabrication.
  • Maintain a laboratory notebook and other technical documentation to required GLP/GMP guidelines.
  • Maintain active dialogue with Regulatory Affairs as subject matter expert on all product design elements/documentation pertaining to research towards FDA/regulated authority submissions,
  • Provide support to marketing and sales team, support the introduction of new technologies with the development of presentations, sales tools, formulations, and applications data
  • Communicate results to the scientific community via published papers. Present research at academic/industry symposia as an external representative of the company.
  • Manage part-time staff as a research leader and mentor for ongoing research projects.
  • Work with company leadership to evaluate existing research practices and contribute to a culture of ethical, high-quality research operations within the organization.
  • Provide other project or product support as needed in order to support Cresilon's business objective.
  • Responsibilities may include other duties as assigned and as required.

Requirements
Required Qualifications
  • BS in Chemical Engineering, Polymer Engineering, Material Science, Biomedical Engineering, Mechanical Engineering, or related scientific discipline.
  • A minimum of 5+ years of product development experience is required.
  • A minimum of 4 years of hands-on experience in new product research and development in a cGMP-regulated industry is required (work experience in the Medical Device field is strongly preferred)
  • Adept experimentalist with hands-on experience in product development of medical devices and their safety/efficacy characterization in an R&D environment.
  • Experience gathering user needs, translating them to technical inputs, and developing viable V&V (Design Verification and Validation) plans.
  • Experience leading complex product development initiatives from concept through product launch/release.
  • Good working knowledge of anatomy and surgical procedures is required.
  • Demonstrated ability to solve difficult technical problems and deliver practical solutions that meet the application requirements is required. This includes strong analytical, problem-solving, and decision-making skills with the ability to be observant and to think creatively.
  • Demonstrated ability to design experiments and analyze data with appropriate quality and statistical methodologies.
  • Demonstrated ability to work independently as well as effectively be a strong team contributor and work cross-functionally to expedite the completion of critical project tasks
  • Ability to handle multiple project assignments of medium scope and complexity and able to prioritize and complete work with a sense of urgency in a timely manner.
  • Ability to lead directly and by influence, including strong problem-solving, conflict resolution, and analytical skills.
  • Requires strong leadership skills, excellent written and verbal communication and presentation skills.
  • Working knowledge of FDA requirements as per 21 CFR 820, ISO 9001, ISO 13485:2003, and ISO 14971:2007.
  • Working knowledge of Good Documentation Practices (GDP), and Good Manufacturing Practices (cGMP)
  • Good understanding of statistical tools and validation/verification techniques.
  • Proficiency in the use of Microsoft Excel, Microsoft Word, and Microsoft PowerPoint is required.
  • Legal authorization to work in the United States is required.

Preferred Qualifications
  • An advanced degree (MS or Ph.D.) is strongly preferred.
  • Hands-on experience in product development with Class II and Class III medical devices.
  • Experience developing test methods and protocols/reports for safety and efficacy testing of implant and instrument designs.
  • Experience with IDE and PMA submissions.
  • Six-Sigma green belt or black belt certification

Cresilon is an equal-opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, training, and apprenticeship. Cresilon makes hiring decisions based solely on qualifications, merit, and business needs at the time.
Benefits
  • Competitive annual base salary range of $100,000 - $160,000, depending upon job level and qualifications
  • Paid Vacation, Sick, & Holidays
  • Monthly MetroCard Reimbursement
  • 401(k) & Roth Retirement Savings Plan with company match up to 5%
  • Work/Life Employee Assistance Program
  • Company Paid Life and Short-Term Disability Coverage
  • Medical, Dental, and Vision Insurance, FSA: Dependent & Healthcare, Commuter & Parking Benefits, Long Term Disability Coverage

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