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Medical Device Development Jobs in California (NOW HIRING)

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... medical device assemblies. * Performs routine assignments according to specified and/or ... development and support centers globally. We are a MBE (NMSDC), WBE (WBENC), and WOSB certified ...

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Associate, Project Manager

Irvine, CA · On-site

$120K - $130K/yr

Stay updated on emerging technologies and industry trends in medical device development. * Stakeholder Management: * Facilitate communication and collaboration between different departments ...

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... medical device assemblies. * Performs routine assignments according to specified and/or ... development and support centers globally. We are a MBE (NMSDC), WBE (WBENC), and WOSB certified ...

New

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Perform assembly, repair, and testing of medical device products. * Work under a microscope while ... development and support centers globally. We are a MBE (NMSDC), WBE (WBENC), and WOSB certified ...

New

Medical Device R&D Engineer

San Jose, CA · On-site

$115K - $175K/yr

Minimum 5 years of medical device R&D experience * Hands-on catheter prototyping and testing experience required * Experience working within ISO 13485 Design Controls required * Experience with ...

We are seeking a Requirements Tools Engineer to support medical device product development by managing enterprise requirements management tools and ensuring regulatory compliance. The role involves ...

... support new medical device development. This role combines advanced technical expertise with project leadership to ensure molds and research and development components are built accurately ...

Showing results 41-60

Medical Device Development information

See California salary details

$28.6K

$52.7K

$79.9K

How much do medical device development jobs pay per year?

As of Aug 6, 2026, the average yearly pay for medical device development in California is $52,718.00, according to ZipRecruiter salary data. Most workers in this role earn between $41,900.00 and $59,200.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in medical device development, and why are they important?

To thrive in Medical Device Development, you need expertise in engineering or life sciences, a solid understanding of regulatory requirements, and often an advanced degree such as a master's or Ph.D. in a relevant field. Familiarity with CAD software, prototyping tools, and knowledge of FDA or ISO regulatory standards is typically required. Strong problem-solving abilities, collaboration, and effective communication distinguish top professionals in this field. These skills ensure the development of safe, innovative, and compliant medical devices that meet both user needs and regulatory standards.

What is the difference between Medical Device Development vs Medical Device Quality Assurance?

AspectMedical Device DevelopmentMedical Device Quality Assurance
CredentialsEngineering degrees, certifications like RAPS or regulatory trainingQuality certifications, ISO 13485, regulatory compliance training
Work EnvironmentDesign labs, R&D teams, product development settingsManufacturing sites, quality control labs, compliance departments
Industry UsageDesigning and creating new medical devicesEnsuring devices meet quality and regulatory standards

Medical Device Development focuses on designing and creating new medical devices, involving engineering and product innovation. Medical Device Quality Assurance ensures these devices meet safety, quality, and regulatory standards through testing and compliance processes. Both roles are essential in the medical device industry but serve different functions in the product lifecycle.

What are some common challenges faced by professionals in medical device development, and how can they be addressed?

Professionals in medical device development frequently encounter challenges such as navigating complex regulatory requirements, ensuring product safety and efficacy, and managing cross-functional collaboration between engineering, clinical, and regulatory teams. Addressing these challenges requires staying updated on evolving regulations, fostering open communication among diverse team members, and implementing robust quality control processes. Proactively engaging with regulatory bodies and regularly reviewing project milestones can help streamline development and reduce the risk of costly delays.

What is medical device development?

Medical device development is the process of designing, creating, testing, and bringing medical devices to market. This process involves multiple stages, including concept development, prototyping, preclinical and clinical testing, regulatory approval, and manufacturing. The goal is to ensure that new devices are safe, effective, and meet regulatory standards before they are used by healthcare professionals or patients. Teams in medical device development often include engineers, scientists, regulatory specialists, and quality assurance professionals.
What are popular job titles related to Medical Device Development jobs in California? For Medical Device Development jobs in California, the most frequently searched job titles are:
What cities in California are hiring for Medical Device Development jobs? Cities in California with the most Medical Device Development job openings:
Infographic showing various Medical Device Development job openings in California as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 23% Part Time, 2% Temporary, and 5% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $52,718 per year, or $25.3 per hour.

Design Engineer II

Applied Medical

Rancho Santa Margarita, CA • On-site

Full-time

Medical, Life, Retirement, PTO

Re-posted 17 days ago


Applied Medical rating

8.0

Company rating: 8.0 out of 10

Based on 23 frontline employees who took The Breakroom Quiz


Job description

Applied Medical is a new generation medical device company with a proven business model and commitment to innovation fueled by rapid business growth and expansion. Our company has been developing and manufacturing advanced surgical technologies for over 30 years and has earned a strong reputation for excellence in the healthcare field.  Our unique business model, combined with our dedication to delivering the highest quality products, enables team members to contribute in a larger capacity than is possible in typical positions.


Position Description

The Design Engineer II contributes to Applied Medical's Technology and Development Mechanical team by designing and developing medical device components, assemblies, and fixtures that directly support the advancement of surgical technology. Working onsite at Applied Medical's global headquarters, this role operates within a cross-functional team environment to take products from concept through detailed design, documentation, and integration into the manufacturing process. The Design Engineer II applies mechanical engineering principles, Computer-Aided Design (CAD) modeling, and hands-on prototyping skills to solve complex design challenges and deliver solutions that meet rigorous quality and regulatory standards. Professionals with backgrounds in mechanical design engineering, biomedical device development, product development engineering, or manufacturing engineering will find this role a strong fit.

Key Responsibilities

  • Design and develop medical device components, assemblies, and fixtures using CAD software, including two-dimensional and three-dimensional modeling and detailed engineering drawings in SolidWorks.
  • Prepare and maintain comprehensive design documentation, including drawings, specifications, design reviews, and supporting technical materials that meet Applied Medical's quality and regulatory standards.
  • Apply Geometric Dimensioning and Tolerancing (GD&T) principles to ensure design intent is accurately communicated and manufacturable within specification.
  • Build and test physical prototypes hands-on to validate design concepts, evaluate performance, and identify opportunities for improvement prior to production.
  • Identify and resolve design issues by analyzing root causes, generating solution concepts, and implementing changes in a structured and documented manner.
  • Collaborate with cross-functional teams, including engineers, product managers, and manufacturing teams, to ensure seamless integration of designs into the broader product development process.
  • Contribute to design reviews, risk analyses, and validation activities in support of regulatory compliance and product quality objectives.
  • Stay current on engineering principles, materials, manufacturing processes, and emerging design technologies relevant to medical device development.

Success in This Role Looks Like

  • Delivering detailed, accurate, and manufacturable design documentation that supports smooth handoffs to manufacturing and cross-functional partners.
  • Producing prototype iterations that meaningfully advance design validation and reduce development risk within established project timelines.
  • Applying sound engineering judgment to identify design problems early and implement well-reasoned solutions independently and within a team setting.
  • Building effective working relationships across engineering, manufacturing, and product management that keep design integration on track.
  • Demonstrating consistent growth in technical depth and design ownership, taking on increasingly complex components and assemblies over time.
  • Upholding Applied Medical's standards for design quality, documentation accuracy, and regulatory compliance across every phase of the development process.

Position Requirements

This position requires the following skills and attributes:

  • Two to three years of relevant mechanical or product design engineering work experience.
  • Bachelor's degree in Mechanical Engineering, Biomedical Engineering, Industrial Engineering, Manufacturing Engineering, or an equivalent field.
  • Proficiency in CAD modeling and drafting, including experience with SolidWorks or comparable three-dimensional design software.
  • Working knowledge of Geometric Dimensioning and Tolerancing (GD&T) and its application in engineering drawings and design specifications.
  • Hands-on experience building and evaluating physical prototypes as part of an iterative product development process.
  • Strong technical writing skills with the ability to prepare and maintain clear, complete design documentation.
  • Excellent organizational and communication skills with the ability to work effectively in cross-functional team environments.
  • Demonstrated ability to analyze complex systems, identify root causes, and develop innovative solutions independently.

Preferred

The following skills and attributes are preferred:

  • Experience in the medical device industry, with familiarity with surgical applications and clinical needs.
  • Understanding of manufacturing and quality standards, including Food and Drug Administration (FDA) regulations and ISO quality systems.
  • Exposure to Failure Mode and Effects Analysis (FMEA) and Test Method Validation processes.
  • Experience with product lifecycle management software, including SAP NetWeaver or equivalent Product Lifecycle Management (PLM) platforms.
  • Experience using Minitab or other statistical analysis software for design verification and validation activities.
  • Experience applying Finite Element Analysis (FEA) and hand calculations to evaluate component strength, stress, and reliability.

Benefits
  • Competitive compensation range: $75000 - $95000 / year (California).
  • Comprehensive benefits package.
  • Training and mentorship opportunities.
  • On-campus wellness activities.
  • Education reimbursement program.
  • 401(k) program with discretionary employer match.
  • Generous vacation accrual and paid holiday schedule.

Please note that the compensation range may be based on factors such as relevant education, qualifications, experience. The compensation range may be adjusted in the future, and special discretionary bonus or incentive compensation plans may apply.

Our total reward package reflects our commitment to team member growth and well-being, as we invest in your development and offer a range of benefits designed to enhance your career and life.

Equal Opportunity Employer

Applied Medical is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, disability (mental and physical), exercising the right to family care and medical leave, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, political affiliation, race, religious creed, sex (including pregnancy, childbirth, breastfeeding and related medical conditions), or sexual orientation, or any other status protected by federal, state or local laws in the locations where Applied Medical operates.

Qualifications:

This position requires the following skills and attributes:

  • Two to three years of relevant mechanical or product design engineering work experience.
  • Bachelor's degree in Mechanical Engineering, Biomedical Engineering, Industrial Engineering, Manufacturing Engineering, or an equivalent field.
  • Proficiency in CAD modeling and drafting, including experience with SolidWorks or comparable three-dimensional design software.
  • Working knowledge of Geometric Dimensioning and Tolerancing (GD&T) and its application in engineering drawings and design specifications.
  • Hands-on experience building and evaluating physical prototypes as part of an iterative product development process.
  • Strong technical writing skills with the ability to prepare and maintain clear, complete design documentation.
  • Excellent organizational and communication skills with the ability to work effectively in cross-functional team environments.
  • Demonstrated ability to analyze complex systems, identify root causes, and develop innovative solutions independently.
Education:UNAVAILABLEEmployment Type: FULL_TIME

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