Onsite Medical Device QMS & FDA Inspection Readiness Consultant
The FDA Group
The FDA Group is seeking an experienced Medical Device Quality Systems Consultant to support the startup of a new Class I medical device contract manufacturing operation in the Atlanta/Duluth area. The consultant will lead QMS implementation, establish auditable processes, and ensure readiness for upcoming FDA inspection as the go-live approaches on November 1. This onsite engagement requires hands-on support across production, warehousing, inventory, traceability, and direct‑to‑consumer #J-18808-Ljbffr The FDA Group
Vacancy posted 6 days ago
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