MedTech Supplier Quality Engineer: Process Validation & CAPA
Listed on 2026-10-14
-
Quality Assurance - QA/QC
Quality Engineering -
Engineering
Quality Engineering
Actalent in Englewood, CO is seeking a Supplier Quality Engineer to strengthen supplier performance and integrate QMS processes. You will review supplier processes, validate data, and perform Cp/Cpk studies to ensure regulatory compliance.
This contract role offers hands-on exposure to medtech quality systems in a cross-functional team. Ideal candidates have 2+ years in supplier quality or quality engineering, knowledge of ISO and FDA QSR/QMSR environments, and experience with CAPA and audits.
Are you ready to take on the Med Tech Supplier Quality Engineer:
Process Validation & CAPA role at Actalent?
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
The position is based in Englewood, CO, United States.
This opportunity is part of our work in Bio & Pharmacology & Health, Management & Operations, Engineering.
(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).