Quality Engineer - Medical Device, CAPA & Process Excellence
Listed on 2026-10-11
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Quality Assurance - QA/QC
Quality Engineering
Job Diva, Inc. in Cambridge, MA seeks a Quality & Regulatory Specialist to monitor manufacturing quality and ensure compliance with FDA 21 CFR Part 820, ISO 13485, and GMP. You will manage CAPA, conduct root cause analyses, and support audits with cross-functional teams.
The role includes maintaining QMS documentation (SOPs, DHF, DMR, DHR), driving continuous improvement with Lean Six Sigma, and ensuring traceability of records across production and quality systems.
We have an opening for a Quality Engineer
- Medical Device, CAPA & Process Excellence in Cambridge, MA, United States within Bio & Pharmacology & Health, Engineering.
We appreciate your interest in this position.
Join Job Diva, Inc. and contribute to our ongoing work.
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This posting is for the Quality Engineer
- Medical Device, CAPA & Process Excellence role at Job Diva, Inc., based in Cambridge, MA, United States.
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