Site Quality Leader – Medical Devices, ISO 13485 & FDA
Listed on 2026-10-18
-
Quality Assurance - QA/QC
Quality Engineering, Regulatory Compliance Specialist
Balda-C-Brewer is seeking a Senior Manager, Site Quality in Ontario, CA to lead the quality department ensuring ISO 13485 and FDA 21 CFR 820 compliance. You will manage validation, metrology, calibration, and product release activities within a continuous improvement framework.
The role requires leadership across audits and customer concerns. Responsibilities include developing and enforcing QA programs, training, and cross-functional collaboration with manufacturing, with a strong focus on
We have an opening for a Site Quality Leader – Medical Devices, ISO 13485 & FDA in Ontario, CA, United States within Management & Operations, Engineering.
We would love to welcome a new Site Quality Leader – Medical Devices, ISO 13485 & FDA to our team in Ontario, CA, United States.
For the Site Quality Leader – Medical Devices, ISO 13485 & FDA position at Balda-C-Brewer, we are reviewing applications now.
(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).