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Biomedical Engineering Consulting Jobs in California

Truvian Sciences

Director, Software Engineering

San Diego, CA · On-site

$268K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... engineers, consultants, contractors, and external development partners. * Cross-functional ... Biomedical Engineering, or related discipline. * 10+ years of software engineering experience ...

Truvian Sciences

Director, Software Engineering

San Diego, CA · On-site

$205 - $220/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... engineers, consultants, contractors, and external development partners. * Cross-functional ... Biomedical Engineering, or related discipline. * 10+ years of software engineering experience ...

DHD Consulting

Medical Technical Support Engineer

San Diego, CA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Bachelor's degree in Mechanical Engineering, Electrical Engineering, Biomedical Engineering, or a related field. * Proficiency in both English and Korean. * Entry-level position: 2+ years of relevant ...

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All JobsBiomedical Engineering Consulting JobsBiomedical Engineering Consulting Jobs in California

Biomedical Engineering Consulting information

See California salary details

$40.5K

$93.6K

$138.2K

How much do biomedical engineering consulting jobs pay per year?

As of Aug 18, 2026, the average yearly pay for biomedical engineering consulting 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 is biomedical engineering consulting?

Biomedical engineering consulting involves providing expert advice and solutions related to the design, development, and implementation of medical devices, healthcare technologies, and related systems. Consultants in this field help organizations navigate regulatory requirements, improve product designs, troubleshoot technical issues, and ensure compliance with industry standards. They often work with hospitals, medical device companies, and research institutions to optimize processes and bring innovative products to market safely and efficiently.

How do biomedical engineering consultants typically collaborate with clients and multidisciplinary teams during a project?

Biomedical engineering consultants frequently work alongside clients such as hospitals, medical device companies, or research institutions, as well as multidisciplinary teams including clinicians, regulatory specialists, and product designers. Effective collaboration often involves participating in regular meetings, clarifying technical requirements, and translating complex engineering concepts for non-technical stakeholders. Consultants also coordinate project timelines, ensure compliance with industry regulations, and provide ongoing technical support throughout the product development or implementation process. Building strong communication and project management skills is essential for thriving in this collaborative environment.

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

To thrive as a Biomedical Engineering Consultant, you need a solid background in biomedical engineering principles, regulatory standards, and a relevant degree, often at the bachelor’s or master’s level. Familiarity with industry-standard tools such as CAD software, statistical analysis programs, and a working knowledge of medical device regulations (like FDA or ISO standards) is crucial. Strong problem-solving skills, effective communication, and the ability to collaborate with multidisciplinary teams set top consultants apart. These skills are vital to ensure innovative, compliant solutions and successful client outcomes in a complex and regulated field.

What is the difference between Biomedical Engineering Consulting vs Biomedical Equipment Technician?

AspectBiomedical Engineering ConsultingBiomedical Equipment Technician
CredentialsBiomedical engineering degree, certifications like CBET or BIETAssociate or bachelor's in biomedical technology, CBET certification
Work EnvironmentConsulting firms, hospitals, medical device companiesHospitals, clinics, service centers
Employer & IndustryConsulting firms, healthcare, medical device industryHealthcare facilities, medical equipment service providers
Job FocusDesign, development, regulatory compliance, project managementMaintenance, repair, calibration of medical equipment

While both roles involve medical devices, Biomedical Engineering Consulting focuses on design, development, and advising on medical systems, whereas Biomedical Equipment Technicians primarily handle maintenance and repair of equipment on-site.

What does a biomedical engineering consulting do?

A biomedical engineering consulting professional provides expertise in designing, evaluating, and improving medical devices, equipment, and systems. They often analyze clinical needs, ensure regulatory compliance, and apply engineering principles to develop innovative healthcare solutions, typically working with cross-disciplinary teams and utilizing tools like CAD software. Their work supports hospitals, medical device companies, and research institutions to enhance patient care and safety.

What are popular job titles related to Biomedical Engineering Consulting jobs in California?

For Biomedical Engineering Consulting jobs in California, the most frequently searched job titles are:

What job categories do people searching Biomedical Engineering Consulting jobs in California look for?

The top searched job categories for Biomedical Engineering Consulting jobs in California are:

What cities in California are hiring for Biomedical Engineering Consulting jobs?

Cities in California with the most Biomedical Engineering Consulting job openings:

Biomedical Engineering Consulting jobs near you
Infographic showing various Biomedical Engineering Consulting job openings in California as of August 2026, with employment types broken down into 80% Full Time, 6% Part Time, and 14% Contract. Highlights an 90% In-person, 3% Hybrid, and 7% Remote job distribution, with an average salary of $93,566 per year, or $45 per hour.

Director, Software Engineering

Truvian Sciences

San Diego, CA • On-site

$268K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 9 days ago

Job description

ABOUT
Want to join a fast-paced, innovative company that is transforming the future of blood testing? Truvian is a healthcare technology company operating at the intersection of diagnostics and consumer technology. We have developed an automated benchtop diagnostic platform that delivers laboratory-quality results in 30 minutes or less across a broad range of health tests.
Our proprietary technology, which has received FDA clearance, is designed to make blood testing more accessible, convenient, and affordable by providing comprehensive results from a single small blood sample in minutes-whether in a retail setting or a private clinic. As we continue to expand access to diagnostic testing, we are actively pursuing CLIA Waiver status to further enable point-of-care testing and bring high-quality healthcare closer to where patients need it most.
To us, our work at Truvian is more than a job - It's a mission. We are a culture dedicated to discovery and empowerment. We are trailblazers on the path to put health information where it belongs - in the hands of the individual. We are partners in the belief that talented people, working as a team, can make every day an adventure. Come join us as we realize our vision to make routine health testing convenient, affordable, and actionable for today's connected consumers!
JOB SUMMARY
Truvian is seeking a Director of Software Engineering to lead software development for its recently FDA-cleared blood testing platform, TruVerus(TM). This role will follow software development life cycle and oversee development and V&V across instrument software, application software, cloud connectivity, cybersecurity, and software quality systems in support of an FDA-regulated product. This is an ONSITE role and local candidates highly preferred.
The ideal candidate has direct experience in managing regulated IVD or medical device software through development, verification and validation, regulatory submission, commercial deployment, and post-market support.
HERE'S WHY YOU'LL LOVE THIS JOB:
  • Unique Growth Opportunity: Gain hands-on experience across clinical studies, assay development, data analysis, regulatory submissions, and product development.
  • Data-Driven Innovation: Work alongside experienced leaders, contributing to real-world healthcare solutions backed by rigorous data.
  • Fast-Paced Start-Up Culture: Be part of an agile, mission-driven team where your work has immediate impact.
  • Meaningful Impact: Help bring innovative diagnostic products to market that can improve patient outcomes.
  • You love and thrive in a fast-paced and dynamic environment where you can implement fresh ideas, new processes, and make things happen quickly without a bunch of red tape
  • You'll have great perks such as:
    • Generous Benefits (Medical/Dental/Vision/EAP/Paid Life Insurance/LTD/401K),
    • Flexible vacation
    • Kombucha and cold brew on tap, craft coffee, a variety of healthy snacks
    • Onsite gym
    • Farm to table onsite restaurant including a 30% discount
WHAT YOU WILL DO:
  • Software leadership: Lead software strategy, roadmap planning, architecture, development, release management, and lifecycle support for Truvian's diagnostic platform.
  • Regulated product development: Ensure software requirements, risk management, design controls, verification, validation, documentation, and release activities are executed in compliance with applicable quality and regulatory requirements.
  • IVD platform support: Support software for instrument control, assay execution, algorithm integration, result generation, connectivity, cloud services, customer-facing applications, and future menu expansion.
  • Quality and regulatory partnership: Work closely with Quality and Regulatory Affairs on FDA submissions, audits, software documentation, deficiency responses, complaint investigations, CAPAs, and post-market support.
  • Cybersecurity and reliability: Lead secure software development practices, vulnerability management, software updates, configuration management, product reliability, and field issue resolution.
  • Team leadership: Build, mentor, and manage a high-performing software engineering team, including internal engineers, consultants, contractors, and external development partners.
  • Cross-functional collaboration: Partner with Engineering, Assay Development, Operations, Manufacturing, Field Service, Quality, and Regulatory teams to support product performance and customer experience.

WHAT YOU WILL BRING:
The ideal candidate will possess:
  • BS, MS, or PhD in Computer Science, Computer Engineering, Software Engineering, Electrical Engineering, Biomedical Engineering, or related discipline.
  • 10+ years of software engineering experience, including 5+ years leading software engineering teams.
  • Direct experience developing FDA-regulated medical device, IVD, diagnostic instrument, laboratory system, or point-of-care diagnostic software.
  • Experience working within design control, software lifecycle, risk management, verification and validation, and quality system environments.
  • Strong understanding of IEC 62304 and regulated software development practices.
  • Experience supporting commercial products after launch, including software maintenance, release management, issue resolution, and post-market support.
  • Experience with cloud-connected products and cloud platforms such as AWS, Azure, or Google Cloud.
  • Strong communication and cross-functional leadership skills in a regulated product development environment.

NICE-TO-HAVE QUALIFICATIONS
  • Experience with IVD analyzers, clinical chemistry, hematology, immunoassay, molecular diagnostics, or point-of-care diagnostic platforms.
  • Experience with LIS, HL7, EMR/EHR integrations, healthcare interoperability, or laboratory informatics.
  • Experience supporting FDA submissions, software documentation, cybersecurity documentation, audits, inspections, or software-related deficiency responses.
  • Experience leading external development partners or geographically distributed technical teams.
SUPERVISORY ROLE
  • Yes
SALARY RANGE
$205,000 - $220,000
The salary range for this position represents the anticipated range for qualified candidates. Compensation decisions are based on a variety of factors, including relevant experience, skills, education, training, certifications, internal equity, market data, and business needs. The final compensation offered to a successful candidate will be determined based on these factors and the requirements of the role.
PHYSICAL DEMANDS AND ABILITIES
  • Ability to safely lift, carry, and move materials weighing up to 5 pounds on a regular basis.
  • Ability to remain stationary and move about the work environment as needed to perform job duties.
  • Ability to perform visual tasks associated with the position, including reviewing data, inspecting materials, and operating laboratory or computer equipment, as applicable.
  • Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions of the position.

Interested candidates are encouraged to submit a cover letter along with their resume. The cover letter is an opportunity to highlight how your experience in assay and/or panel architecture aligns with our mission, your approach to technical leadership and cross-functional collaboration, and how your expertise has driven innovation in diagnostic product development and complex assay systems.
Truvian is an Equal Opportunity Employer and is committed to fostering a diverse, inclusive, and respectful workplace. Employment decisions are made based on qualifications, merit, and business needs. Truvian prohibits discrimination, harassment, and retaliation and does not discriminate on the basis of any characteristic protected by applicable federal, state, or local law, including race, color, religion, creed, sex, pregnancy (including childbirth, breastfeeding, and related medical conditions), gender, gender identity, gender expression, sexual orientation, national origin, ancestry, age, physical or mental disability, medical condition, genetic information, marital status, military or veteran status, reproductive health decision-making, or any other legally protected status.
This policy applies to all aspects of employment, including recruitment, hiring, placement, promotion, compensation, benefits, training, transfers, leaves of absence, disciplinary actions, termination, and all other terms and conditions of employment. Truvian is also committed to providing reasonable accommodations to qualified individuals with disabilities and to applicants and employees with sincerely held religious beliefs, practices, or observances, in accordance with applicable law.

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