Medical Device Quality Assurance Leader
Listed on 2026-10-07
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Quality Assurance - QA/QC
Regulatory Compliance Specialist
The Suddath Companies is seeking a Quality Assurance Manager to lead the site quality program for medical device operations, including contract manufacturing, kitting, packaging, and distribution. You will ensure FDA 21 CFR Part 820/QMSR and ISO 13485 alignment, investigations, CAPA, and audit readiness while partnering across functions.
Strong regulatory knowledge, leadership, and a track record in continuous improvement are essential for success in this role.
Join us at The Suddath Companies as our next Medical Device Quality Assurance Leader in Duluth, GA, United States.
The position is based in Duluth, GA, United States.
This opportunity is part of our work in Management & Operations, Engineering.
The advertised compensation is 110..
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
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