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No Experience Biomedical Engineer Jobs in California

Apple

Biomedical Research Engineer

Cupertino, CA

$129K - $225K/yr

In addition experience in the following areas will be a plus for this role: Coherent light sensing ... MS/PhD in Biomedical, Optical Engineering or related field. Minimum Qualifications In-depth ...

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No Experience Biomedical Engineer information

What is a no experience biomedical engineer?

A No Experience Biomedical Engineer job is an entry-level position designed for recent graduates or individuals transitioning into the biomedical field without prior professional experience. These roles typically involve assisting with research, product development, testing, or regulatory compliance in healthcare and medical device industries. Employers may provide training and mentorship to help you develop technical skills and industry knowledge. Strong problem-solving abilities, a solid foundation in engineering principles, and a willingness to learn are key qualities for success in this role.

What types of tasks and responsibilities can I expect as a no experience biomedical engineer?

As a biomedical engineer starting with no experience, you'll often support senior engineers by assisting with laboratory experiments, data analysis, documentation, and the testing or calibration of biomedical equipment. You may participate in team meetings, help with troubleshooting technical problems, or contribute to research and development projects under supervision. Your daily work is likely to be collaborative, involving close interaction with engineers, scientists, and potentially healthcare professionals. Entry-level roles provide broad exposure to the field, allowing you to develop technical skills and understand how engineering solutions are applied in medical contexts. These foundational experiences are crucial for advancing to more specialized or independent roles in the future.

What are the key skills and qualifications needed to thrive as a no experience biomedical engineer?

To thrive as a No Experience Biomedical Engineer, you typically need a relevant bachelor's degree in biomedical engineering or a related field, with a solid understanding of biology, engineering principles, and mathematics. Familiarity with software tools such as MATLAB, CAD, or simulation programs is beneficial, and some entry-level roles may encourage pursuing certifications like EIT (Engineer-in-Training). Strong teamwork, effective communication, and a willingness to learn help you quickly adapt and contribute in multidisciplinary environments. These skills ensure you can bridge knowledge gaps, collaborate on projects, and grow into more complex responsibilities as your career progresses.

What are the most commonly searched types of Biomedical Engineer jobs in California?

The most popular types of Biomedical Engineer jobs in California are:

What are popular job titles related to No Experience Biomedical Engineer jobs in California?

For No Experience Biomedical Engineer jobs in California, the most frequently searched job titles are:

What job categories do people searching No Experience Biomedical Engineer jobs in California look for?

The top searched job categories for No Experience Biomedical Engineer jobs in California are:

What cities in California are hiring for No Experience Biomedical Engineer jobs?

Cities in California with the most No Experience Biomedical Engineer job openings:

No Experience Biomedical Engineer jobs near you
Infographic showing various No Experience Biomedical Engineer job openings in California as of August 2026, with employment types broken down into 70% Full Time, 15% Part Time, and 15% Contract. Highlights an 92% In-person, and 8% Hybrid job distribution.

Engineer, Biomedical/Medical Device

3 Key Consulting

Newbury Park, CA • On-site

Full-time

Re-posted 16 days ago

Job description

Engineer, Biomedical/Medical Device

3 Key Consulting is recruiting an Engineer for a consulting engagement with our direct client, a leading global biopharmaceutical company.

The Device Engineer will participate in the medical device/combination product design, development, and commercialization activities for drug delivery devices, focusing on prefilled syringes.

Top Must Have Skill Sets:

  • Hands on Laboratory Experience in a GLP Setting- 1+ years of experience.
  • Good Communication and Technical Writing Skills
  • Ability to Multitask
  • Must have BS degree Mechanical or Biomedical Engineering, or related field.

Day to Day Responsibilities:

  • Test procedure development and functional test execution
  • Authoring technical plans and reports
  • Performing statistical data analysis
  • Supporting technical assessments and root cause investigations
  • Transfer of information to manufacturing sites, engagement with suppliers
  • Maintenance of Design History File content consistent with Good Documentation Practices

Basic Qualifications:

  • Fully competent engineer in all conventional aspects of the subject matter, functional area, and assignments.
  • Plans and conducts work requiring judgment in the independent evaluation, selection, and adaptation and modification of standard techniques/procedures/criteria, and devises new approaches to encountered challenges.
  • Generates and maintains design specifications, protocol and report writing, prototyping, design of experiments/statistical process control product optimization, design verification & validation, FMEA, etc.
  • System level root cause investigation; CAD/SolidWorks proficiency; tolerance analysis; capability analysis.
  • Coordinate and implement design improvements with development partners.
  • Collaborate with scientists and engineers internally and externally to assess and develop appropriate design and manufacturing specifications.
  • Accountability of maintaining technical records within product design history files.
  • Individual contributor with leadership attributes to effectively represent device engineering within a large network/matrix organization.
  • Working proficiency and familiarity with governing standards and regulations, including Quality System Regulation (21CFR820) and Risk Management (ISO 14971).

Preferred Qualifications:

  • Degree in the field of Mechanical or Biomedical Engineering, or related field
  • Medical device industry and/or regulated work environment experience
  • Excellent written and verbal communication skill
  • Development/commercialization of medical devices and knowledge of manufacturing processes
  • Initiating and bringing complex projects to conclusion
  • Ability to work independently and dynamic cross functional teams
  • Design controls
  • Failure investigation
  • Applied statistics

Red Flags:

  • No laboratory experience or desire to work in a lab environment (not considering less than a year)
  • No desire to work in cross-functional team environment
  • Poor communication and technical writing skills
  • Many positions in a short time frame (e.g. 3 per year)
  • Interested in remote-only; this job requires on-site attendance

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