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Internship R&D Engineer Medical Device Jobs in Riverside, CA

Alcon

Principal, Software Engineer

Lake Forest, CA · On-site

$143K - $192K/yr

The Principal Software Engineer, Medical Device Systems is responsible for maintaining, enhancing, and supporting software for Alcon's on-market ophthalmic medical devices and imaging platforms. This ...

VOLT

Medical Device Assembler - 2nd Shift

Irvine, CA · On-site

$18 - $19.75/hr

Come create your career with Volt Volt is immediately hiring a Medical Device Assembler - 2nd Shift ... D, 401(k), Sick time, and other types of paid leaves (as required by law), Employee Assistance ...

Techlink Systems

Be Seen First

Medical Device Assembler DN2025

Irvine, CA · On-site

$19 - $19.75/hr

Hand soldering. d. Cleanroom environment. e. Maintain written and electronic documentation. * This ... medical device assemblies. * Performs routine assignments according to specified and/or ...

Intellectt INC

Medical device Assembler

Irvine, CA · On-site

$19.25 - $23.50/hr

... assembly of medical devices as well as setting up, operating, performing maintenance on and ... engineering with equipment maintenance. · Supports R&D builds. · Maintains organization of ...

Techlink Systems

Be Seen First

Medical Device Assembler - CM2025

Irvine, CA · On-site

$19.75/hr

Hand soldering. d. Cleanroom environment. e. Maintain written and electronic documentation. * This ... medical device assemblies. * Performs routine assignments according to specified and/or ...

New

R.D. Olson

Project Manager

Irvine, CA · On-site

Project Manager - R.D. Olson Construction | SoCal Southern California | Commercial GC | Hospitality ... engineering wins and track profitability ✔ Mentor PEs and APMs -- grow the next generation ✔ ...

R D Olson Construction

Project Manager

Irvine, CA · On-site

$96K - $140K/yr

Project Manager - R.D. Olson Construction | SoCal Southern California | Commercial GC | Hospitality ... engineering wins and track profitability • Mentor PEs and APMs - grow the next generation • ...

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All JobsR&D Engineer Medical Device JobsInternship R&D Engineer Medical Device JobsInternship R&D Engineer Medical Device Jobs in Riverside, CA

Internship R D Engineer Medical Device information

See Riverside, CA salary details

$11

$20

$30

How much do internship r&d engineer medical device jobs pay per hour?

As of Jul 23, 2026, the average hourly pay for internship r&d engineer medical device in Riverside, CA is $20.15, according to ZipRecruiter salary data. Most workers in this role earn between $16.78 and $21.83 per hour, depending on experience, location, and employer.

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 cities near Riverside, CA are hiring for Internship R&D Engineer Medical Device jobs? Cities near Riverside, CA with the most Internship R&D Engineer Medical Device job openings:
Internship R D Engineer Medical Device jobs near you
Principal, Software Engineer

Principal, Software Engineer

Alcon

Lake Forest, CA • On-site

$143K - $192K/yr

Full-time

Medical, Life, Retirement

Posted 7 days ago

Alcon rating

7.5

Company rating: 7.5 out of 10

Based on 67 frontline employees who took The Breakroom Quiz

260th of 535 rated manufacturers

Job description

At Alcon, we're passionate about enhancing sight and helping people see brilliantly. With more than 25,000 associates, we innovate fearlessly, champion progress, and act swiftly to impact global eye health. We foster an inclusive culture, recognizing your contributions and offering opportunities to grow your career like never before. Together, we make a difference in the lives of our patients and customers. Are you ready to join us?
The Principal Software Engineer, Medical Device Systems is responsible for maintaining, enhancing, and supporting software for Alcon's on-market ophthalmic medical devices and imaging platforms. This role requires a strong background in C++, C#, hardware/software interfaces, and medical device or instrumentation systems, with highly desired experience in MATLAB, camera integration, imaging technologies, firmware interaction, FPGA-based systems, LabVIEW, and RTOS environments. The engineer will investigate software anomalies, assess the impact of hardware and component changes, support cybersecurity and compliance initiatives, and implement robust software solutions that ensure product performance, reliability, and patient safety throughout the product lifecycle.
The role serves as a key liaison between engineering, customer-facing teams, product security, verification and validation, and global software development organizations. It ensures that software changes are properly assessed, documented, tested, and released in accordance with quality system requirements and medical device regulations.
The Principal Software Engineer collaborates closely with onshore and offshore development and V&V teams throughout the software development lifecycle, providing technical inputs for testing, validating software modifications, supporting troubleshooting activities, and maintaining software configuration management. The role enables successful delivery of software updates while ensuring adherence to company policies, regulatory requirements, and product quality standards.
This is an onsite position located at our main campus in Lake Forest, California.
In this role, a typical day will include:
  • Primary function is to code and/or software updates for on-market medical device systems.
  • Collaborate closely with the software development teams, Technical Support, Field Service, Manufacturing, Clinical and other operation organizations to support necessary software changes initiated by reported anomalies, changes in use cases, material or hardware changes that impact software, cybersecurity, regulatory updates, and other.
  • Troubleshoot, and define solutions to meet expectations, and incorporate changes according to defined processes and procedures, in line with industry standards and regulations.
  • Maintain configuration management and change control according to the associated product Configuration Management Plan and Change Control procedures.
  • Document and execute change-related unit and integration tests. Provide inputs for scope, impact, and effective test methodologies for testing.
  • Assure compliance to software release procedures for post-Market changes to on-market products.
  • Travel required, est. 10-20%

Key Requirements/Minimum Qualifications:
  • Bachelor's Degree or Equivalent years of directly related experience (or high school +13 yrs.
  • Assoc.+9 yrs.; M.S.+2 yrs.; PhD+0 yrs.)
  • The ability to fluently read, write, understand, and communicate in English
  • 5 Years of Relevant Experience

Preferred Qualifications:
  • Technical Development Methodology for Medical Devices (21 CFR 820.30, ISO 13485)
  • Systems Engineering or Risk Management for Medical Device (ISO 14971)
  • Medical Device Software - Software Life Cycle Processes (IEC 62304)
  • Regulations and Guidelines associated with software development for medical device
  • Microsoft Office suite (i.e., Word, Excel, Visio)
  • Must have C++, C# development experience.
  • Must have a background with hardware/software interfaces within RTOS and Windows environments.
  • Highly desired skills: MatLAB, LabView, FPGA, Firmware, and experience with camera interactions and interfaces.
  • Familiar with object-oriented software design and large software architecture.
  • Ability to work cross-functionally with a variety of stakeholders.
  • Ability to work independently, proactively identify issues, recommend, and implement solutions, and deliver quality
  • results on schedule while managing multiple tasks and internal customers.
  • Solid understanding of Window operating environments (Win11, Win10, etc.)
  • Experience with one or more software configuration management systems and related tools, such as: AWS DevOps,
  • Jira, Git, ADO, GitHub, TFS
  • Knowledge of networking and cybersecurity concepts are a plus.
  • Experience with Microsoft Visual Studios or other integrated development environment (IDE) tools
  • Prior experience creating and executing software testing at unit, sub-system, integration, and system levels.
  • Familiar with FDA/ISO regulations for software development and/or EUMDR, prefer including IEC 62304
  • Understanding of Software Development Lifecycle Management (SDLC) - (Agile/Scrum, iterative)
  • Good interpersonal & Communication skills to build positive departmental and inter-departmental relationships in a
  • virtual, remote, and asynchronous environment.
  • Medical device experience is preferred

How to Thrive at Alcon:
ATTENTION: Current Alcon Employee/Contingent Worker
If you are currently an active employee/contingent worker at Alcon, please click the appropriate link below to apply on the Internal Career site.
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Compensation and Benefits
Alcon's Total Rewards programs are designed to align incentives with business objectives, support our values, and deliver long-term value. Our compensation approach includes a combination of fixed and variable pay, with short-term and long-term incentive opportunities for eligible roles. Our benefits offerings are designed to support associates and their families across key life events, including programs that promote health and well-being, provide financial security, and support retirement planning.
The salary range posted represents the anticipated hiring range for this role. Actual compensation may vary based on factors such as experience, skills, location, and internal equity, and may fall outside the posted range.
Pay Range
128,350.00 - 166,100.00
Pay Frequency
Annual
Alcon is an Equal Opportunity Employer and participates in E-Verify. Alcon takes pride in maintaining a diverse environment and our policies are not to discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity, marital or veteran status, disability, or any other legally protected status. Alcon is also committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an email to alcon.recruitment@alcon.com and let us know the nature of your request and your contact information.

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