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Director Engineering Medical Device Jobs (NOW HIRING)

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 ...

IT MINDS L.L.C.

Quality Engineer - Medical Device

Newark, DE · On-site

$70K - $90K/yr

Quality Engineer - Medical Device Location: Delaware Largescale Medical Device client facing a ... Technical Review & Support • Review engineering drawings and specifications to confirm accuracy ...

Collabera

Medical device engineer

North Chicago, IL

... days, Medical, Dental and Vision insurance, 401K retirement savings plan, Life Insurance ... Evaluate and integrate relevant engineering advances for improving or solving problems Understand ...

Kelly Services

CAE Engineer - (Medical Device)

Mahwah, NJ · On-site

$45 - $55/hr

Pay: Negotiable depending on direct-related experience up to $45 - $55 an hour We are seeking a ... Bachelor's Degree in a science or engineering discipline. * 2+ years of experience with modeling ...

TEEMA

Lead Swift/iOS Medical Device SWE

San Diego, CA · On-site

$175K - $210K/yr

Lead iOS (Swift) Software Engineer - Medical Device Startup We're partnering with a well-funded, fast-growing startup to hire a Lead iOS/Swift Software Engineer. This is a high-impact, full-time role ...

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Director Engineering Medical Device information

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$73K

$194.7K

$254K

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

As of Jun 9, 2026, the average yearly pay for director engineering medical device in the United States is $194,709.00, according to ZipRecruiter salary data. Most workers in this role earn between $141,500.00 and $253,000.00 per year, depending on experience, location, and employer.

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 key skills and qualifications needed to thrive in the Director Engineering Medical Device position, and why are they important?

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 is a Director Engineering Medical Device job?

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.

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What cities are hiring for Director Engineering Medical Device jobs? Cities with the most Director Engineering Medical Device job openings:
What are the most commonly searched types of Engineering Medical Device jobs? The most popular types of Engineering Medical Device jobs are:
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Director Engineering Medical Device jobs near you
Infographic showing various Director Engineering Medical Device job openings in the United States as of May 2026, with employment types broken down into 17% As Needed, 49% Full Time, 17% Part Time, and 17% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $194,709 per year, or $93.6 per hour.

Medical Device R&D Engineer

AngioSafe

San Jose, CA • On-site

$115K - $175K/yr

Full-time

Posted 9 days ago

Job description

AngioSafe is a Bay Area start-up focused on improving healthcare through state-of-the-art vascular interventional catheter device design, development, and manufacturing. We are pioneering the development of novel treatment mechanisms and algorithms to provide unprecedented access to peripheral and coronary disease treatments. Our experienced team is committed to developing and commercializing innovative, high-quality products that reduce risk and improve cardiovascular treatment outcomes. This onsite role will have a meaningful and direct impact on AngioSafe's device portfolio through the development of novel vascular interventional devices and support of existing product pipelines. The ideal candidate will combine strong engineering fundamentals with hands-on technical ability and thrive in a fast-paced startup environment.
Position Summary
We are seeking a highly motivated, hands-on Individual Contributor (IC) R&D Engineer to support the design, development, prototyping, testing, and manufacturing transfer of interventional catheter devices.This role is ideal for someone who enjoys building and testing devices directly, solving technical challenges, and working collaboratively within a small, rapidly evolving medical device company.
Roles and Responsibilities
  • Contribute to the design, development, testing, and manufacturing transfer of interventional catheter devices
  • Support development activities for both new and existing products
  • Perform hands-on prototyping, assembly, troubleshooting, and testing of medical devices
  • Generate technical documentation in accordance with Design Control requirements
  • Develop test methods, protocols, and reports for:
    • concept evaluations
    • verification & validation testing
    • component qualification
    • packaging and shelf-life validation
  • Support creation and maintenance of:
    • Bills of Materials (BOMs)
    • manufacturing process instructions
    • engineering specifications
    • risk management documentation
  • Work closely with suppliers to support component development and resolve non-conformance issues
  • Assist in maintaining shared laboratory and prototype spaces
  • Collaborate cross-functionally with engineering, manufacturing, quality, and leadership teams

Minimum Qualifications
  • Bachelor's degree in Mechanical Engineering or related engineering discipline preferred
  • 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 document control systems and engineering change documentation
  • Strong hands-on engineering and troubleshooting abilities
  • Startup and/or small-company experience preferred
  • Proficiency with SolidWorks including:
    • 3D component and assembly modeling
    • 2D drawings per ASME Y14.5
  • Knowledge of catheter manufacturing materials and processes including:
    • braiding
    • lamination
    • laser welding
    • adhesive bonding
    • packaging
  • Strong communication and technical writing skills
  • Ability to manage multiple priorities in a fast-paced environment
  • Self-motivated with strong ownership mentality

Preferred Qualifications
  • Catheter design and development experience strongly preferred
  • Experience supporting FDA and/or Notified Body submissions
  • Experience using cloud-based document control systems
  • Project leadership experience preferred

Additional Information
  • This is a fully onsite role based in San Jose, CA
  • No relocation or immigration sponsorship available
  • Principals only please

Equal Opportunity Employer
AngioSafe is committed to a diverse workplace and is committed to equal opportunity employment for all job applicants without regard to race, color, religion, sex, sexual orientation, age, gender, gender identity or expression, size, national origin, disability, or veteran status. AngioSafe complies with all applicable local, state, and national laws governing non-discrimination in employment

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