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Director Engineering Medical Device Jobs in California

Pride Global

Medical Device Engineer

San Diego, CA · On-site

$82.66 - $96.43/hr

We are seeking a Senior Medical Device Engineer to join our Research & Development team. In this ... Bachelor's degree in Materials Science, Polymer Science, Chemical Engineering, Biomedical ...

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SlingShot Connections

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Medical Device Assembler

San Clemente, CA · On-site

$22.10/hr

Work under direction from management or engineering staff with direct oversight * Other duties as ... Comfortable working in a regulated environment (medical device experience is a plus) * Ability to ...

AngioSafe

Medical Device R&D Engineer

San Jose, CA · On-site

$115K - $175K/yr

This onsite role will have a meaningful and direct impact on AngioSafe's device portfolio through ... The ideal candidate will combine strong engineering fundamentals with hands-on technical ability ...

AngioSafe

Medical Device R&D Engineer

San Jose, CA · On-site

$115K - $175K/yr

This onsite role will have a meaningful and direct impact on AngioSafe's device portfolio through ... The ideal candidate will combine strong engineering fundamentals with hands-on technical ability ...

Crown Medical, Inc.

Medical Device Rep

Carlsbad, CA · On-site

$82K - $113K/yr

Medical Sales Territory Representative - Entry Level We are a leading Medical Device and Equipment ... as directed by management in order to grow market share; * Consistently develop a partnership ...

Talentry, LLC

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Sr. Mechanical Engineer - Medical Device

San Diego, CA · On-site

$130K - $180K/yr

Senior Mechanical Engineer - Medical Device San Diego, CA (Onsite) 130,000-180,000 DOE Join a ... What you bring: · BS in Mechanical Engineering or related field; MS preferred. · Approximately 5+ ...

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All JobsEngineering Medical Device JobsDirector Engineering Medical Device JobsDirector Engineering Medical Device Jobs in California

Director Engineering Medical Device information

See California salary details

$72K

$192.2K

$250.7K

How much do director engineering medical device jobs pay per year?

As of Aug 19, 2026, the average yearly pay for director engineering medical device in California is $192,160.00, according to ZipRecruiter salary data. Most workers in this role earn between $139,600.00 and $249,700.00 per year, depending on experience, location, and employer.

What is a director engineering medical device?

A Director of Engineering in the medical device industry leads the design, development, and testing of medical technologies while ensuring compliance with regulatory standards. They manage engineering teams, oversee project timelines, and collaborate with cross-functional departments, including R&D, quality assurance, and manufacturing. Their role involves strategic planning, resource allocation, and risk management to drive innovation and bring safe, effective medical devices to market.

What are the key skills and qualifications needed to thrive in the director engineering medical device position?

To excel as a Director Engineering Medical Device, you need extensive experience in engineering management, regulatory compliance (such as FDA and ISO standards), and a background in medical device design or related technical fields. Proficiency with product lifecycle management (PLM) tools, design control systems, and quality management certifications like Six Sigma or PMP are highly valuable. Outstanding leadership, strategic thinking, and the ability to communicate effectively across multidisciplinary teams help set top performers apart. These capabilities are crucial to successfully guide high-stakes projects, ensure regulatory compliance, and drive innovation in a highly regulated industry.

What are the typical challenges faced by a director of engineering in the medical device industry?

A Director of Engineering in the medical device field often navigates complex regulatory requirements while balancing innovation and speed-to-market. They frequently manage cross-functional teams, oversee rigorous testing and verification processes, and must ensure that all products meet strict quality and safety standards. Collaboration with regulatory, clinical, and marketing teams is essential to align technical development with business objectives. Additionally, adapting to evolving technology and changes in regulatory landscapes can present ongoing challenges, making strong leadership and adaptability key assets.

What are the most commonly searched types of Engineering Medical Device jobs in California?

The most popular types of Engineering Medical Device jobs in California are:

What are popular job titles related to Director Engineering Medical Device jobs in California?

For Director Engineering Medical Device jobs in California, the most frequently searched job titles are:

What job categories do people searching Director Engineering Medical Device jobs in California look for?

The top searched job categories for Director Engineering Medical Device jobs in California are:

What cities in California are hiring for Director Engineering Medical Device jobs?

Cities in California with the most Director Engineering Medical Device job openings:

Director Engineering Medical Device jobs near you
Infographic showing various Director Engineering Medical Device job openings in California as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 12% Part Time, and 6% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $192,160 per year, or $92.4 per hour.

Electrical Product Engineering (Medical Device)

Siri InfoSolutions Inc

Irvine, CA • On-site

Contractor

Re-posted 29 days ago

Job description

Job Title: Electrical Product Engineering (Medical Device)

Location: Irvine, CA (Onsite)

Experience: 6–8 Years

We are seeking a skilled and motivated Electrical Engineer to support Continuous Improvement Projects (CIP) within a dynamic medical device environment. This role involves working closely with cross-functional teams and external suppliers to drive cost optimization, product enhancements, and design improvements while ensuring compliance with regulatory and quality standards.

Key Responsibilities:

Lead and execute Continuous Improvement Projects (CIP) in collaboration with internal stakeholders and external suppliers

Perform cost analysis and CIP calculations, including evaluation of supplier quotations

Develop and manage project budgets, considering feasibility, capital equipment, validation costs, and testing requirements (e.g., DVT, bioburden where applicable)

Create and maintain detailed project plans using Microsoft Project and prepare presentations using PowerPoint

Apply strong knowledge of electrical design, product architecture, and system functionality

Drive design changes, component substitutions, and supplier transitions to achieve cost savings and performance improvements

Develop innovative strategies to meet cost reduction and performance goals

Conduct engineering testing, create test protocols, generate reports, and lead design reviews

Oversee project timelines, dependencies, and execution strategies to ensure successful delivery

Identify appropriate electrical test methods and align requirements with R&D teams

Support process validation activities and complete required documentation (RR forms, validation reports, etc.)

Manage and execute change requests and supplier change control processes

Ensure adherence to health, safety, environmental, and regulatory standards

Communicate project updates, risks, and opportunities to management

Provide technical guidance to junior engineers or technicians when required

Perform additional duties as assigned

Required Skills & Qualifications

6–8 years of experience in Electrical/Product Engineering, preferably in the medical device industry

Strong experience in Continuous Improvement (CIP) and cost optimization initiatives

Solid understanding of electrical design, system architecture, and product lifecycle

Hands-on experience with testing, validation (DVT), and documentation

Knowledge of medical device regulations and quality standards (e.g., FDA, ISO)

Experience working with suppliers, sourcing, and cost evaluation

Proficiency in Microsoft Project and PowerPoint

Strong analytical, problem-solving, and communication skills

Preferred / Nice-to-Have Skills

Experience supporting Splash Team Projects

Familiarity with bioburden testing and advanced validation processes

Prior experience in supplier transition and change management

Siri Infosolutions logo

About Siri Infosolutions

Sourced by ZipRecruiter

Our team of experts first gather each and every requirement of yours. Our research and development team then sit around those requirements and come up with a plan. Our implementation team then executes that plan for optimal results. After that our support team remains in constant touch with you during and after the entire process.

Industry

It services

Company size

201 - 500 Employees

Headquarters location

Edison, NJ, US

Year founded

2005

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