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Internship R&D Engineer Medical Device Jobs in California

Medical Device R&D Engineer

San Jose, CA ยท 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 ...

Medical Device R&D Engineer

San Jose, CA ยท 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 ...

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Medical Device Assembler

San Clemente, CA ยท On-site

$20.25 - $22.27/hr

Support engineering tests by executing defined test methods * Record and maintain documentation as ... Comfortable working in a regulated environment (medical device experience is a plus) * Ability to ...

Quality Engineer

Los Gatos, CA ยท On-site

$95K - $120K/yr

... medical device innovation hub focused on the development of novel medical products to address ... Collaborate closely with cross-functional teams, including Operations and R&D. * Support Operations ...

Medical Device Assembler

Irvine, CA ยท On-site

$18 - $19.67/hr

Come create your career with Volt Volt is immediately hiring a Medical Device Assembler in Irvine ... D, 401(k), Sick time, and other types of paid leaves (as required by law), Employee Assistance ...

Collaborate with multiple departments, including Q&R, R&;D, Engineering, and document control, to ... Pharmaceutical and/or medical device experience preferred. * Understanding of cGMP, ISO13485, and ...

Project Engineer - R.D. Olson Construction | SoCal Sedona, AZ & Southern California | Commercial GC | Hospitality + Multifamily This isn't just another construction job. It's your launchpad. At R.D.

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Internship R D Engineer Medical Device information

What does an Internship R&D Engineer in Medical Device do?

An Internship R&D Engineer in Medical Device assists in the research and development of new medical technologies and products. Their responsibilities typically include supporting senior engineers in designing, testing, and improving medical devices, conducting experiments, collecting and analyzing data, and preparing technical documentation. Interns also learn about regulatory standards and industry best practices while working as part of a multidisciplinary team. This role is ideal for students or recent graduates looking to gain hands-on experience in medical device innovation.

What are the key skills and qualifications needed to thrive as an Internship R&D Engineer in Medical Devices, and why are they important?

To thrive as an Internship R&D Engineer in Medical Devices, you generally need a background in biomedical engineering or a related field, with strong analytical and problem-solving abilities. Familiarity with CAD software, lab equipment, and basic knowledge of regulatory standards like ISO 13485 is important, and prior internships or relevant coursework can be advantageous. Attention to detail, effective communication, and collaborative teamwork skills help you contribute meaningfully to projects and navigate cross-functional environments. These skills ensure you can support innovative product development while adhering to strict safety and quality standards in the medical device industry.

What is the difference between Internship R&D Engineer Medical Device vs R&D Engineer Medical Device?

AspectInternship R&D Engineer Medical DeviceR&D Engineer Medical Device
QualificationsEnrolled in or recent graduate of engineering/biomedical programsBachelor's or Master's in engineering/biomedical fields
Work EnvironmentInternship programs, entry-level projects, supervised tasksFull-time, independent project work, team collaboration
ResponsibilitiesAssisting in research, testing, and documentationDesign, develop, and improve medical device products
Industry UsageCommonly used for training and entry-level experienceCore role in product development and innovation

In summary, the Internship R&D Engineer Medical Device is an entry-level position designed for students or recent graduates gaining initial industry experience. The R&D Engineer Medical Device is a full-time professional role with greater responsibilities in product development and innovation within the medical device industry.

What types of projects or tasks can an Internship R&D Engineer expect to work on in the medical device industry?

As an Internship R&D Engineer in the medical device industry, you can expect to be involved in a variety of projects such as prototyping new device concepts, conducting laboratory experiments, performing data analysis, and supporting design verification and validation activities. Interns often collaborate closely with multidisciplinary teams, including senior engineers, regulatory specialists, and clinicians, to help solve real-world problems and improve patient outcomes. This hands-on experience provides valuable insight into the product development lifecycle and offers opportunities to contribute to meaningful projects that can enhance your technical and professional skills.
What are the most commonly searched types of R&D Engineer Medical Device jobs in California? The most popular types of R&D Engineer Medical Device jobs in California are:
What cities in California are hiring for Internship R&D Engineer Medical Device jobs? Cities in California with the most Internship R&D Engineer Medical Device job openings:
Infographic showing various Internship R&D Engineer Medical Device job openings in California as of June 2026, with employment types broken down into 50% Full Time, and 50% Part Time. Highlights an 100% In-person job distribution.

Software Engineer/ Medical Device Development- Product Development - Remote

MILLENNIUMSOFT

San Diego, CA โ€ข On-site, Remote

Other

Posted 25 days ago


Job description

Position : Softwareย Engineer/ย Medical Device Development- Product Development - Remote

Location : San Diego, CA

Duration : 12 Months

Total Hours/week : 40.00

1st Shift

Client : Medical Devices Company

Job Category : Professional

Level of Experience : Senior Level

Employment Type : Contract on W2 (Need US Citizens or GC Holders or GC EAD or OPT or EAD or CPT)

Job Description:

  • We are seeking a highly skilled, drive, and experienced Staff Process Engineer (Software) with expertise in defining and implementing software design and development processes and design control deliverables that adhere to regulatory standards within the medical device industry.
  • This role requires a strong technical background in Software Engineering, leadership capabilities, and extensive experience in product design and development.
  • Experience in Quality and/or Systems Engineering is also a plus.
  • The engineer will play a critical role in shaping the process for defining and documenting software-centric design control elements and deliverables, as well as the software development process itself, ensuring alignment with regulatory requirements such as FDA guidance, and meeting both user and business needs.
  • They will also be remediating the design control documentation for accuracy, completeness, and clear upstream and downstream traceability from software-centric design control elements.
  • The ideal candidate will lead continuous improvement efforts, collaborate across multi-disciplinary teams, and provide technical expertise to ensure successful project outcomes.

Key Responsibilities

  • Software Process Definition: Develop and implement software processes that comply with industry standards and regulations (e.g., IEC 62304, FDA guidance, IEEE standards), with a focus on the complete software development life cycle.
  • Software Design Documentation Remediation: Develop or modify and implement software design documentation templates within the Quality Management System that comply with industry standards and regulations. Clearly demonstrate end-to-end traceability where software design control elements are included, and remediate gaps and errors as needed.
  • Leadership: Translate business and regulatory requirements into comprehensive software development processes. Conduct back testing and work collaboratively to ensure alignment with additional stakeholders, development teams, and business objectives. Maintain frequent and clear communication with team members and leaders working in all areas of the project. Identify risks and issues early on and implement mitigations as necessary.
  • Cross-Functional Collaboration: Facilitate effective knowledge sharing and collaboration across departments (e.g., Systems Engineering, Hardware Engineering, Test Engineering, Quality, and others) to resolve alignment or feasibility issues. Communicate relevant project information effectively (verbal and written) including project status, technical concepts and design details, and functional demonstrations to key internal and external stakeholders of varying technical abilities.
  • Continuous Improvement: Identify and drive opportunities for process improvement within the Software Engineering function to enhance efficiency, quality, clarity, and compliance.
  • Technical Expertise: Serve as a resource for addressing and resolving issues of process and documentation. Apply best practices from methodologies like DFSS (Design for Six Sigma) and Critical Parameter Management to all projects. Review and remediate software design control documentation.

Minimum Qualifications

Education & Experience

  • Bachelorโ€™s degree in Science or Engineering is required; a postgraduate degree is preferred
  • Minimum of 5 years of related work experience in software engineering, medical device development, or similar fields; experience with regulatory standards (e.g., IEC 62304, FDA guidance, IEEE standards) in a regulated industry is highly preferred
  • Demonstrated ability to lead multi-disciplinary engineering teams and serve as a technical leader within the organization
  • Positive attitude with an aptitude for critical thinking
  • Willingness to learn and adapt to new challenges
  • Strong organizational skills, ability to work independently and with a group
  • Ability to handle multiple tasks simultaneously and prioritize workload

Technical Skills

  • Strong background in software engineering and test, and requirements management
  • Experience in software product development, including user needs assessment, software system analysis, architectural design, integration and testing, Reliability Engineering, Project Management, and Failure Modes Effects Analysis
  • Extensive experience in the creation and maintenance of design and development documentation is preferred
  • Knowledge and experience with methodologies like DFSS or statistical test design and analysis is preferred
  • Experience in Quality engineering and design control management is a plus
  • Experience with ALM/PLM tools is a plus
  • Exceptional communication skills, both interdepartmental and cross-functional
  • Strong writing abilities and attention to detail are essential
  • Experience working in an agile development environment is a plus
  • The candidate must be legally authorized to work in the United States without limitations and require no sponsorship for visa status now or in the future (e.g. H1-B status)

This is a hybrid position. Remote work may be considered on a case-by-case basis.