Senior Biomedical Engineer - Regulatory & Lifecycle Leader
-
Engineering
Job Description & How to Apply Below
Ventis Medical, a Princeton, NJ-based developer of the Hero Vent, seeks a Principal Biomedical Engineer with 8–10+ years of medical device experience. This on-site role leads QMSR/ISO compliance, design controls, DHF ownership, and cross‑functional collaboration with CM, suppliers, and test labs across full product lifecycle.
You will bridge advanced device design with regulatory requirements, drive V&V, risk management per ISO 14971 and IEC 60601, and guide audits and regulatory submissions
This is a strong opening to take on the Senior Biomedical Engineer
- Regulatory & Lifecycle Leader role at Ventis Medical, Inc.
The advertised compensation is 150..
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Senior Biomedical Engineer
- Regulatory & Lifecycle Leader role in the description above.
Position Requirements
10+ Years work experience(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
View / Apply for Jobs
Matching My Jurisdiction