ZipRecruiter

Log In

2

Full Time Manager Engineering Medical Device Jobs

AngioSafe

Medical Device R&D Engineer

San Jose, CA · On-site

$115K - $175K/yr

... medical device company. Roles and Responsibilities * Contribute to the design, development, testing ... instructions * engineering specifications * risk management documentation * Work closely with ...

AngioSafe

Medical Device R&D Engineer

San Jose, CA · On-site

$115K - $175K/yr

... medical device company. Roles and Responsibilities * Contribute to the design, development, testing ... instructions * engineering specifications * risk management documentation * Work closely with ...

Therakos

Medical Device Service Engineer

Madison, WI

Manage and/or participate in related project work as assigned * Ensure compliance with Quality ... Collaborate with engineering, quality, and product teams to escalate issues and support continuous ...

Clinical Search Group, LLC

Be Seen First

Associate Territory Manager

Westchester, NY · On-site

$65K - $70K/yr

... Clinical Engineers, Medical Science Liaisons, Medical Device Sales Reps, Medical Device Sales ... Manager with the best Medical Device Companies.

Microvision Inc

Medical Device Assembler

Seabrook, NH · On-site

$18 - $20/hr

Time Management. * Thoroughness. Supervisory Responsibility This Position has no supervisory ... Position Type/Expected Hours of Work This is a full-time position. Days and hours of work are ...

next page

Showing results 1-20

All JobsFull Time Manager Engineering Medical Device Jobs

Full Time Manager Engineering Medical Device information

See salary details

$46.5K

$146.9K

$174K

How much do full time manager engineering medical device jobs pay per year?

As of Jun 21, 2026, the average yearly pay for full time manager engineering medical device in the United States is $146,868.00, according to ZipRecruiter salary data. Most workers in this role earn between $116,500.00 and $173,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Full Time Manager Engineering in Medical Devices, and why are they important?

To thrive as a Full Time Manager Engineering in Medical Devices, you need a solid background in engineering principles, regulatory compliance (such as FDA or ISO standards), and a relevant engineering degree. Familiarity with technical tools like CAD software, project management systems, and medical device development platforms, as well as certifications like PMP or Six Sigma, is highly valued. Exceptional leadership, communication, and problem-solving skills help you effectively manage teams and coordinate cross-functional projects. These competencies ensure that innovative, safe, and compliant medical devices are delivered efficiently to market.

What are some common challenges faced by a Full Time Manager in Engineering for Medical Devices, and how can they be addressed?

A Full Time Manager in Engineering for Medical Devices often faces challenges balancing regulatory compliance with timely project delivery. Navigating complex FDA or international standards while leading multidisciplinary teams can be demanding. Effective communication, proactive risk management, and fostering a culture of continuous improvement help address these issues. Building strong relationships across regulatory, R&D, and manufacturing teams also ensures smoother collaboration and innovation within a highly regulated environment.

What is a Full Time Manager Engineering Medical Device?

A Full Time Manager Engineering Medical Device is a professional responsible for overseeing engineering teams involved in the design, development, and production of medical devices. This role involves managing projects, ensuring regulatory compliance, coordinating with cross-functional teams, and driving innovation while meeting quality and safety standards. The manager also mentors engineering staff, allocates resources, and works closely with other departments such as quality assurance, manufacturing, and regulatory affairs to bring medical devices from concept to market.
More about Full Time Manager Engineering Medical Device jobs
What cities are hiring for Full Time Manager Engineering Medical Device jobs? Cities with the most Full Time Manager Engineering Medical Device job openings:
What states have the most Full Time Manager Engineering Medical Device jobs? States with the most job openings for Full Time Manager Engineering Medical Device jobs include:
What job categories do people searching Full Time Manager Engineering Medical Device jobs look for? The top searched job categories for Full Time Manager Engineering Medical Device jobs are:
Full Time Manager Engineering Medical Device jobs near you
Infographic showing various Full Time Manager Engineering Medical Device job openings in the United States as of June 2026, with employment types broken down into 87% Full Time, 2% Part Time, 1% Temporary, and 10% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $146,868 per year, or $70.6 per hour.

Medical Device R&D Engineer

AngioSafe

San Jose, CA • On-site

$115K - $175K/yr

Full-time

Posted 21 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

Apply