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Medical Device Design Engineer Jobs in California

Elve Inc

Amplifier Design Engineer

Davis, CA · On-site

... amplifier device design * Master's degree in Electrical Engineering or a related field with at ... Health benefits (medical, dental, vision) * Vacation time * A taste of the start‑up life

Elve Inc

Amplifier Design Engineer

Davis, CA · On-site

... amplifier device design * Master's degree in Electrical Engineering or a related field with at ... Health benefits (medical, dental, vision) * Vacation time * A taste of the start-up life * Exposure ...

Elve Inc

Amplifier Design Engineer

Davis, CA · On-site

... amplifier device design * Master's degree in Electrical Engineering or a related field with at ... Health benefits (medical, dental, vision) * Vacation time * A taste of the start-up life * Exposure ...

Elve Inc

Amplifier Design Engineer

Davis, CA

... amplifier device design * Master's degree in Electrical Engineering or a related field with at ... Health benefits (medical, dental, vision) * Vacation time * A taste of the start-up life * Exposure ...

Elve Inc

Amplifier Design Engineer

Davis, CA · On-site

... amplifier device design * Master's degree in Electrical Engineering or a related field with at ... Health benefits (medical, dental, vision) * Vacation time * A taste of the start-up life * Exposure ...

Cspeed

Laser Design Engineer (Epi/Device)

Palo Alto, CA · On-site

We are seeking a Senior Laser Design Engineer to own device design and simulation for this laser array, working in a small, cross-functional team where individual contributions are highly visible and ...

Noblesoft Technologies

SW Design engineer

Alameda, CA · On-site

Technical Documentation (GDP) - SW Design engineer for Software integration Testing We need ... medical device. * Understand the GUI design developed in C++ language for micro-controller based ...

Talent Space, Inc.

Sr. Design Engineer

Fremont, CA · On-site

Evaluate device performance through electrical and optical characterization and recommend design ... Analyze engineering data, troubleshoot technical issues, and drive continuous improvements in ...

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All JobsMedical Device Design Engineer JobsMedical Device Design Engineer Jobs in California

Medical Device Design Engineer information

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How much do medical device design engineer jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for medical device design engineer in California is $49.18, according to ZipRecruiter salary data. Most workers in this role earn between $34.62 and $58.85 per hour, depending on experience, location, and employer.

What does a medical device design engineer do?

A Medical Device Design Engineer is responsible for designing and developing medical devices that improve patient care and meet regulatory standards. They work on creating prototypes, testing designs, and ensuring products are safe, effective, and manufacturable. Their role often involves collaborating with healthcare professionals, regulatory specialists, and manufacturing teams. They also stay up to date with technological advancements and compliance requirements in the medical industry.

What skills and qualifications are needed to thrive as a medical device design engineer?

To thrive as a Medical Device Design Engineer, you need a solid background in biomedical engineering, mechanical engineering, or a related field, with expertise in product development and regulatory compliance. Familiarity with CAD software, prototyping tools, and standards such as ISO 13485 and FDA regulations is typically required. Strong problem-solving abilities, creativity, and effective communication skills set top performers apart in this role. These competencies are crucial for developing innovative, safe, and regulatory-compliant medical devices that improve patient outcomes.

How does a medical device design engineer collaborate with cross-functional teams during product development?

Medical Device Design Engineers regularly work alongside professionals from regulatory, quality assurance, clinical, and manufacturing teams. They participate in design reviews, translate clinical needs into technical requirements, and ensure designs meet safety and compliance standards. Effective communication and teamwork are essential, as engineers must incorporate feedback, address concerns from various stakeholders, and document changes throughout the development lifecycle. This collaborative approach helps ensure the final product is both effective and compliant with industry regulations.

What is the difference between Medical Device Design Engineer vs Mechanical Engineer?

AspectMedical Device Design EngineerMechanical Engineer
Required CredentialsBachelor's in biomedical, mechanical engineering, or related; certifications like Certified Biomedical Equipment Technician (CBET) are commonBachelor's in mechanical engineering; optional certifications like Professional Engineer (PE)
Work EnvironmentMedical device companies, healthcare settings, R&D labsManufacturing, automotive, aerospace, R&D labs
Industry UsageDesigning and developing medical devices, ensuring regulatory complianceDesigning mechanical systems across various industries

Medical Device Design Engineers focus on creating and refining medical devices, ensuring they meet health regulations and user needs. Mechanical Engineers have a broader scope, working on mechanical systems in multiple industries. While both roles require engineering fundamentals, Medical Device Design Engineers specialize in healthcare applications and regulatory standards.

Medical Device Design Engineer jobs near you
Infographic showing various Medical Device Design Engineer job openings in California as of September 2026, with employment types broken down into 61% Full Time, and 39% Contract. Highlights an 100% In-person job distribution, with an average salary of $102,304 per year, or $49.2 per hour.

Engineer, Device Engineering

San Diego, CA • On-site

Scorpion Therapeutics
51 - 200 employees
Learn more about Scorpion Therapeuticsexternal

Other

Posted 8 days ago

Job description

Responsibilities
  • Develop and execute strategies and technical roadmaps for drug-device combination product development.
  • Provide technical leadership from concept through commercialization and lifecycle management.
  • Lead human factors and usability engineering (formative and summative evaluations).
  • Author/review human factors/usability plans, URRAs, study protocols/reports, and design control documentation.
  • Provide expertise in drug delivery technologies, device design, systems engineering, design controls, risk management, materials, and manufacturing.
  • Lead development of prefilled syringes, autoinjectors, and other drug delivery systems.
  • Collaborate cross-functionally with Product Development, Packaging, Manufacturing, Clinical Development, Supply Chain, Commercial, Quality, and Regulatory Affairs.
  • Oversee external testing laboratories (device characterization/design verification).
  • Establish/maintain design control processes and DHF documentation.
  • Support design transfer (risk assessments, specifications, control strategies, statistical evaluation).
  • Author/review combination product sections of INDs, IMPDs, BLAs, and MAAs.
  • Ensure compliance with FDA/EU device and combination product regulations and standards (ISO 14971, ISO 13485, EU MDR).
  • Identify technical/program risks, manage vendors/partners, and support continuous improvement.
Requirements
  • Bachelor’s in Biomedical Engineering, Mechanical Engineering, Pharmaceutical Sciences, or related.
  • 8+ years’ experience in combination product or medical device development (end-to-end lifecycle).
  • Demonstrated experience with prefilled syringes and autoinjectors.
  • Strong knowledge of subcutaneous drug delivery, device design, systems engineering, materials, and manufacturing.
  • Experience implementing design controls and risk management; leading human factors/usability engineering.
  • In-depth knowledge of FDA/EU regulations and quality systems (ISO 14971, ISO 13485, EU MDR).
  • Experience with device characterization/design verification testing and contributing to regulatory submissions.
  • Strong communication, stakeholder influence, and project management.
Preferred
  • Advanced degree.
  • Experience with biological drug products and primary packaging.
  • cGMP process development, manufacturing controls, process risk assessments, design transfer.
  • Fast-paced/high-growth biotech/pharma experience.
  • Mentoring/technical leadership.
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