What are the responsibilities and job description for the Medical Device R&D Engineer position at AngioSafe, Inc.?
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