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Remote Medical Device Intern Jobs in California (NOW HIRING)

Vaxcyte

Manager, Supplier & Internal Auditor

San Carlos, CA · On-site +1

$151K - $176K/yr

... medical device industries. Essential Functions: * Supplier Audits * Plan, schedule, and conduct supplier audits (on-site and remote) in support of supplier qualification and ongoing oversight ...

Amgen

Scientific Director

Thousand Oaks, CA · On-site +1

The role is hybrid, option for remote work may be available. Key responsibilities include ... Medical Device & Combination Product Support * Provide toxicology expertise supporting ISO 10993 ...

Zoll Medical Corporation

Sr. Project Manager

San Jose, CA · On-site +1

Experience with medical device capital equipment development required and * 10+ years of experience ... For fully remote positions, compensation will comply with all applicable federal, state, and local ...

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Remote Medical Device Intern information

What is a remote medical device intern?

A Remote Medical Device Intern is a student or early-career professional who supports the development, testing, or marketing of medical devices while working remotely. These interns assist with research, documentation, data analysis, and may participate in virtual meetings with engineering, regulatory, or quality assurance teams. The position offers valuable industry experience and exposure to the medical device lifecycle, all while allowing interns to work from home or another remote location. This flexibility makes it accessible for students or candidates who may not be able to relocate or commute.

What are the key skills and qualifications needed to thrive as a remote medical device intern?

To thrive as a Remote Medical Device Intern, you need a solid background in biomedical engineering or a related life sciences field, along with a basic understanding of medical device regulations and standards. Familiarity with CAD software, data analysis tools, and regulatory documentation systems is typically required. Strong communication, self-motivation, and attention to detail are essential soft skills for collaborating with remote teams and handling project tasks independently. These skills ensure you can contribute effectively to product development, maintain compliance, and support innovation in a remote work environment.

How do remote medical device interns typically collaborate with engineering and clinical teams while working off-site?

Remote Medical Device Interns often engage with cross-functional teams through regular video conferences, collaborative project management tools, and shared documentation platforms. Effective communication skills are essential, as interns may attend virtual meetings with engineers, regulatory specialists, and clinical staff to discuss design updates, testing protocols, and feedback on prototypes. Staying proactive in seeking feedback and providing project updates helps ensure smooth collaboration and integration into the team, despite the physical distance.

What are popular job titles related to Remote Medical Device Intern jobs in California?

For Remote Medical Device Intern jobs in California, the most frequently searched job titles are:

What job categories do people searching Remote Medical Device Intern jobs in California look for?

The top searched job categories for Remote Medical Device Intern jobs in California are:

What cities in California are hiring for Remote Medical Device Intern jobs?

Cities in California with the most Remote Medical Device Intern job openings:

Remote Medical Device Intern jobs near you
Infographic showing various Remote Medical Device Intern job openings in California as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 16% Part Time, and 5% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution.

Principal Scientist | REMOTE (Valencia (CA), United States)

Sonova AG

Valencia, CA • On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 17 days ago

Key responsibilities

  • Lead the scientific design, development, and oversight of clinical studies from concept through publication.

  • Develop clinical study protocols, Clinical Study Reports, and other documents supporting regulatory submissions.

  • Support regulatory submissions by leading scientific activities, including justifications and responses to health-authority questions.

Job description

Principal, Clinical Scientist
Valencia, California - Hybrid preferred | REMOTE FOR THE RIGHT CANDIDATE
Join Advanced Bionics as a Principal, Clinical Scientist and provide scientific leadership across global clinical development programs supporting innovative medical device technologies. In this highly collaborative role, you will lead clinical study design, regulatory scientific strategy, evidence generation, and scientific communication across the product lifecycle to support regulatory approvals, indication expansions, and Medical Affairs initiatives.
Responsibilities
  • Lead the scientific design, development, and oversight of pivotal, post-market, investigator-sponsored, and real-world evidence studies from concept and protocol development through study completion and publication.
  • Develop clinical study protocols, Clinical Study Reports (CSRs), literature reviews, and other essential clinical and regulatory documents supporting regulatory submissions.
  • Lead scientific activities supporting regulatory submissions, including scientific justifications, responses to health-authority questions, and scientific interactions with regulatory agencies.
  • Analyze and interpret clinical and scientific evidence to support clinical development, regulatory strategy, evidence generation, and product lifecycle management.
  • Collaborate closely with Regulatory Affairs, Quality Assurance, R&D, external experts, and other cross-functional partners to advance clinical development programs.
  • Lead the development and review of scientific manuscripts, abstracts, posters, presentations, and other scientific publications.
  • Support publication strategies, scientific training, congress presentations, and other activities that communicate and disseminate clinical evidence.

More about you
  • Master's degree in Life Sciences, Health Sciences, or another related scientific discipline.
  • Minimum 8 years of experience in clinical development, clinical research, Medical Affairs, or Scientific Affairs, including protocol development and scientific writing.
  • Demonstrated experience developing clinical study protocols, Clinical Study Reports, regulatory scientific documents, and scientific publications.
  • Strong knowledge of ICH-GCP, ISO 14155, FDA regulations, and medical device clinical development.
  • Excellent scientific writing, analytical, communication, presentation, and project-management skills.
  • Ability to effectively collaborate across global and cross-functional teams and provide scientific leadership to complex programs.
  • Ability to travel approximately 15-25% to scientific congresses, investigator meetings, and other study-related activities.

Preferred qualifications include: a PhD or AuD; experience with Class III medical devices, hearing healthcare, or neuromodulation; experience leading cross-functional scientific initiatives or mentoring junior scientists; experience supporting FDA PMA/IDE, EU MDR, or other global regulatory submissions and health-authority interactions; and experience with reference-management and statistical software.
A minimum of 300Mb/sec download and 10Mb/sec upload speed internet connectivity is required to support any remote/hybrid employee functionality at Sonova.
Don't meet all the criteria? If you're willing to go all in and learn we'd love to hear from you!
We are looking forward to receiving your application via our online job application platform. For this position only direct applications will be considered. Sonova does not recruit via app, telegram, carrier pigeon or any other format that does not include speaking with an actual human. If you are offered a job without speaking with someone please contact Sonova Human Resources.
What we offer
  • Medical, dental and vision coverage*
  • Health Savings, Health Reimbursement, Flexible Spending/Dependent Care Accounts
  • TeleHealth options
  • 401k plan with company match*
  • Company paid life/ad&d insurance
  • Additional supplemental life/ad&d coverage available
  • Company paid Short/Long-Term Disability coverage (STD/LTD)
  • STD/LTD Buy-ups available
  • Accident/Hospital Indemnity coverage
  • Legal/ID Theft Assistance
  • PTO (or sick and vacation time), floating Diversity Day, & paid holidays*
  • Paid parental bonding leave
  • Employee Assistance Program (24/7 mental health support hotline, 5 company paid counseling sessions and more)
  • Robust Internal Career Growth opportunities
  • Tuition reimbursement
  • Hearing aid discount for employees and family
  • Internal social recognition platform

*Plan rules/offerings dependent upon group Company/location.
This role's pay range is between: $131K - $165K. This role is also [bonus eligible/commission eligible, if applicable].
How we work
At Sonova, we prioritize the well-being of our employees and foster an inclusive environment that promotes engagement and collaboration. Our team-customized hybrid work model empowers teams to balance individual needs with business goals, offering flexibility and individualized time management. We recognize the importance of life outside of work and strive to create a supportive and motivating workplace where innovation thrives.
Sonova is an equal opportunity employer
We team up. We grow talent. We collaborate with people of diverse backgrounds to win with the best team in the market place. We guarantee every person equal treatment in regard to employment and opportunity for employment, regardless of a candidate's ethnic or national origin, religion, sexual orientation or marital status, gender, genetic identity, age, disability or any other legally protected status.

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