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Medical Device RD Engineer

Job in San Jose, Santa Clara County, California, 95199, USA
Listing for: AngioSafe
Full Time position
Listed on 2026-06-18
Job specializations:
  • Engineering
    Biomedical Engineer, Medical Device Industry, Manufacturing Engineer, Product Engineer
Salary/Wage Range or Industry Benchmark: 100000 - 125000 USD Yearly USD 100000.00 125000.00 YEAR
Job Description & How to Apply Below

Angio Safe is a Bay Area start-up focusing 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 seasoned experts are committed to developing and commercializing high quality and innovative products to decrease risk and improve outcomes of cardiovascular disease treatment.

This onsite role will have a meaningful and direct impact on Angio Safe’s device portfolio through development of novel vascular interventional devices and support of our existing device pipeline. The ideal candidate will bring both theoretical and hands‑on ability to design and implement new concepts and processes in support of high quality, high capacity and sustainable product lines.

Roles and Responsibilities
  • Lead sub projects and contribute to the design, development, testing, and manufacturing transfer of interventional catheters including sustaining engineering activity for existing products
  • Generate technical documentation of designs, evaluations, and testing in accordance with design control standards
  • Generate test methods, protocols, and reports for concept evaluation, verification & validation, sustaining engineering product design iterations, component qualifications, and packaging/shelf‑life validations
  • Hands on building and/or testing of new and existing devices in the Angio Safe portfolio
  • Oversee R&D technician’s work including testing and prototype assembly
  • Generate new or update existing manufacturing process instructions, bill of materials, product engineering specifications, and risk management documentation
  • Work with suppliers to develop and meet internal component specifications including incoming inspection non‑conformance resolution
  • Help maintain a shared test and prototype lab space
Minimum Skills and Experience
  • 5 years of Medical Device R&D experience
  • Working within ISO 13485 regulated Design Controls
  • Adhering to document controls and completing document change orders
  • Bachelor’s degree in mechanical engineering
  • Hands on catheter prototyping and testing
  • Solid Works skills, including detail component and assembly 3D modeling and 2D specification drawings per ASME Y14.5
  • Knowledge of materials selection and techniques for catheter manufacturing processes including braiding, lamination, laser welding, adhesive bonding, and packaging
  • Effective communicator able to explain technical concepts to all members of the company
  • Solid technical writing skills including the use of Word, Excel, Power Point
  • Awareness and attention to high-level design goals and company direction
  • Ability to organize and prioritize a variety of tasks in a small & rapidly changing organization
  • High-level of maturity and self-motivation
Preferred Skills and Experience
  • Support of regulatory submissions to FDA and Notified Bodies
  • Use of cloud-based Document Control Systems
  • Project leadership/management experience
Principals only Please

Angio Safe 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. Angio Safe complies with all applicable local, state, and national laws governing non‑discrimination in employment.

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