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Biomedical Engineering Related Jobs in California

Masimo

Engineer II, Algorithm

Irvine, CA · On-site

$120K - $150K/yr

Minimum Qualifications: * 2-5 years of related engineering experience in algorithm development, signal processing, biomedical engineering, software engineering, or a related technical discipline ...

Masimo

Engineer II, Algorithm

Irvine, CA · On-site

$120K - $150K/yr

Minimum Qualifications: * 2-5 years of related engineering experience in algorithm development, signal processing, biomedical engineering, software engineering, or a related technical discipline ...

Direct Counsel

Patent Agent/Advisor (Medtech)

San Diego, CA · On-site

$125K - $228K/yr

Degree in materials, chemical, mechanical, or biomedical engineering (or related field) * Broad scientific knowledge in mechanical and/or biomedical engineering * Advanced degree preferred * At least ...

Direct Counsel

Patent Agent/Advisor (Medtech)

Palo Alto, CA · On-site

$125K - $228K/yr

Degree in materials, chemical, mechanical, or biomedical engineering (or related field) * Broad scientific knowledge in mechanical and/or biomedical engineering * Advanced degree preferred * At least ...

OPERATION SMILE INC

Bachelor's degree in biomedical engineering, clinical engineering, or a related field * Strong understanding of medical equipment management, and training in low-resources settings * 5+ years of ...

ADDSOURCE

Staff Reliability Engineer Hardware

San Jose, CA · On-site

$120K - $151K/yr

Bachelor's or Master's degree in Mechanical Engineering, Electrical Engineering, Biomedical Engineering, or a related field. Experience supporting new product development and reliability engineering ...

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All JobsBiomedical Engineering Related JobsBiomedical Engineering Related Jobs in California

Biomedical Engineering Related information

See California salary details

$40.5K

$93.6K

$138.2K

How much do biomedical engineering related jobs pay per year?

As of Aug 10, 2026, the average yearly pay for biomedical engineering related in California is $93,566.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,500.00 and $114,500.00 per year, depending on experience, location, and employer.

What are 5 related careers to biomedical engineers?

Related careers to biomedical engineers include clinical engineers, who manage medical equipment; bioinformatics specialists, who analyze biological data; medical device designers, who develop new equipment; healthcare technology consultants, who advise on system integration; and research scientists in biomedical fields. These roles often require knowledge of biology, engineering principles, and proficiency with specialized tools and software.

What are some common interdisciplinary collaborations for biomedical engineers in a typical work setting?

Biomedical engineers frequently work alongside professionals from various disciplines, including physicians, nurses, clinical researchers, and software developers. These collaborations are essential when designing medical devices, improving diagnostic equipment, or developing new healthcare technologies. Effective communication and teamwork are crucial, as biomedical engineers must translate clinical needs into technical solutions while ensuring regulatory compliance and user safety. Such interdisciplinary teamwork not only enhances project outcomes but also provides valuable learning and networking opportunities for career growth.

What are the key skills and qualifications needed to thrive in biomedical engineering, and why are they important?

To thrive in Biomedical Engineering, you need a solid background in engineering principles, biology, and mathematics, typically supported by a bachelor's or master's degree in biomedical engineering or a related field. Familiarity with CAD software, medical imaging systems, and regulatory standards like FDA or ISO certifications is commonly required. Strong problem-solving, communication, and teamwork skills help professionals collaborate effectively with clinicians and researchers. These abilities are essential to develop innovative medical technologies that are safe, effective, and meet regulatory requirements.

What kind of job does a biomedical engineer get?

A biomedical engineer designs and develops medical devices, equipment, and software used in healthcare settings. They work in hospitals, research labs, or manufacturing companies, often requiring knowledge of biology, engineering principles, and regulatory standards.

What jobs can you go into with biomedical engineering?

Biomedical engineering graduates can pursue careers as biomedical engineers, designing medical devices, equipment, and software. They also work in research and development, quality assurance, regulatory affairs, and clinical engineering, often requiring knowledge of biology, engineering principles, and medical standards.

What is the difference between Biomedical Engineering Related vs Medical Device Technician?

AspectBiomedical Engineering RelatedMedical Device Technician
Required CredentialsBachelor's degree in biomedical engineering or related fieldAssociate's degree or certification in medical device technology
Work EnvironmentResearch labs, hospitals, manufacturing facilitiesHospitals, clinics, repair centers
Employer & Industry UsageMedical device companies, research institutionsHealthcare facilities, medical equipment companies
Common Search & ComparisonOften compared for technical roles in medical device developmentCompared for hands-on maintenance and repair roles

Biomedical Engineering Related roles focus on designing, developing, and testing medical devices, requiring a bachelor's degree and working in research or manufacturing environments. Medical Device Technicians primarily handle installation, maintenance, and repair of medical equipment, often with technical certifications and working directly in healthcare settings. While both roles involve medical devices, their responsibilities, credentials, and work environments differ significantly.

What is a biomedical engineer?

Biomedical engineers apply engineering principles and design concepts to medicine and biology for healthcare purposes. They work on developing medical devices, diagnostic equipment, healthcare software, and artificial organs, among other innovations. Their goal is to improve the quality and effectiveness of patient care by bridging the gap between engineering and medicine. Biomedical engineers often collaborate with doctors, researchers, and other professionals to solve complex healthcare challenges.
What are popular job titles related to Biomedical Engineering Related jobs in California? For Biomedical Engineering Related jobs in California, the most frequently searched job titles are:
What job categories do people searching Biomedical Engineering Related jobs in California look for? The top searched job categories for Biomedical Engineering Related jobs in California are:
Biomedical Engineering Related jobs near you
Infographic showing various Biomedical Engineering Related job openings in California as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, 1% Temporary, and 2% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $93,566 per year, or $45 per hour.

Associate Engineering Director, Combination Drug Product/Device

Neurocrine Biosciences, Inc.

San Diego, CA • On-site

$177K - $183K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 23 hours ago

Job description

Who We Are:
Neurocrine Biosciences is a leading biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs. We are dedicated to discovering, developing and commercializing life-changing treatments for patients with under-addressed neurological, psychiatric, endocrine and immunological disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, hyperphagia in Prader-Willi syndrome, endometriosis* and uterine fibroids*, as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas. For more than three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders, because you deserve brave science. For more information, visit neurocrine.com, and follow the company on LinkedIn, X, Facebook and YouTube. (*in collaboration with AbbVie)
About the Role:
In partnership with the broader CMC organization, the Associate Director of Drug/Device Combination Products will lead the development and lifecycle strategy for drug/device combination products, including prefilled syringe and autoinjector presentations. This role will provide technical ownership for delivery devices and associated primary and secondary packaging from early development through commercialization and post approval lifecycle management.
The successful candidate will serve as a subject matter expert in combination product development, design controls, device engineering, primary packaging, manufacturing readiness, and drug/device integration. This individual will work closely with cross-functional partners across CMC, Clinical, Regulatory, Quality, Manufacturing, Supply Chain, and external development and manufacturing partners to advance a pipeline of injectable products.
Your Contributions (include, but are not limited to):
  • Lead strategic planning and execution of drug/device combination product development for clinical and commercial presentations
  • Provide technical ownership for delivery devices, primary packaging, and related combination product elements across the product lifecycle
  • Develop and implement innovative delivery device solutions, including prefilled syringe, autoinjector, and other injectable delivery platforms
  • Serve as the device and combination product subject matter expert on cross-functional CMC and program teams
  • Lead technical decision-making, risk management, and issue resolution for drug/device integration, device performance, manufacturability, and lifecycle management
  • Ensure timely completion of development, verification, validation, manufacturing, and technology transfer deliverables
  • Partner with Quality, Regulatory, and external suppliers to ensure combination product strategies meet global regulatory, cGMP, safety, and quality expectations
  • Identify, evaluate, engage, and manage external partners for device development, manufacturing, testing, and commercialization activities
  • Monitor external innovation, emerging technologies, connected health solutions, and industry trends in injectable delivery systems
  • Support integration of delivery device and drug product strategies across multiple therapeutic modalities, including peptides, proteins, antibodies, and gene therapy products

Requirements:
  • BS/BA in Mechanical Engineering, Biomedical Engineering, or a related field, with 10+ years of industry experience, OR
  • MS/MA in Mechanical Engineering, Biomedical Engineering, or a related field, with 8+ years of industry experience, OR
  • PhD in Mechanical Engineering, Biomedical Engineering, or a related field, with 5+ years of industry experience
  • Experience developing and commercializing drug/device combination products (e.g., pre-filled syringe systems, autoinjectors) is essential
  • Advanced knowledge of design controls, design verification and validation, risk management, design transfer, and lifecycle management
  • Experience with manufacturing scale-up, technology transfer, and external partner or supplier oversight
  • Thorough understanding of cGMP, quality systems, and global regulatory expectations for combination products and medical devices, including FDA, EMA, and applicable ISO standards
  • Current knowledge of drug delivery technologies, connected health solutions, human factors/usability engineering, and emerging trends in injectable product development
  • Proven ability to solve complex technical challenges, make sound risk-based decisions, and influence cross-functional teams
  • Strong communication, collaboration, and leadership skills in a matrixed environment

Preferred Qualifications
  • Experience supporting regulatory filings, health authority interactions, or commercial launch readiness for combination products
  • Experience working with external device developers, contract manufacturers, testing laboratories, or component suppliers
  • Familiarity with primary container closure systems, secondary packaging, human factors engineering, and device constituent part control strategies
  • Experience supporting products across multiple modalities, including peptides, proteins, antibodies, or gene therapy products

#LI-DM1
Neurocrine Biosciences is an EEO/Disability/Vets employer.
We are committed to building a workplace of belonging, respect, and empowerment, and we recognize there are a variety of ways to meet our requirements. We are looking for the best candidate for the job and encourage you to apply even if your experience or qualifications don't line up to exactly what we have outlined in the job description.
The annual base salary we reasonably expect to pay is $173,600.00-$237,000.00. Individual pay decisions depend on various factors, such as primary work location, complexity and responsibility of role, job duties/requirements, and relevant experience and skills. In addition, this position offers an annual bonus with a target of 30% of the earned base salary and eligibility to participate in our equity based long term incentive program. Benefits offered include a retirement savings plan (with company match), paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage in accordance with the terms and conditions of the applicable plans.

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