Quality Engineer – Medical Devices; ISO/FDA)
Listed on 2026-10-16
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Quality Assurance - QA/QC
Quality Engineering, Regulatory Compliance Specialist
AB Electronics in Danbury, CT is seeking a proactive Quality Engineer to ensure products meet quality standards and regulatory requirements. The role collaborates across teams to implement QA processes and maintain QMS, including FDA regulations and ISO 13485/9001.
Responsibilities include audits, machine qualification, training, and documentation for regulatory submissions, with a focus on continuous improvement and strong communication across functions.
Our team is growing, and we are hiring a Quality Engineer – Medical Devices (ISO 13485/FDA) in Danbury, CT, United States.
The advertised compensation is 90..
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 Quality Engineer – Medical Devices (ISO 13485/FDA) role in the description above.
We appreciate your interest in this position.
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