Quality Assurance
1 month ago
Job summary
The Quality Assurance & Regulatory Affairs Associate is responsible for maintaining and executing quality documentation and compliance activities aligned with ISO 13485, FDA 21 CFR Part 820, MDSAP, as well as ICH-GCP and clinical research quality requirements.<+Responsibilities
+- Maintain and update controlled documents within the QMS in accordance with SOPs and document control procedures. +
- Track document versions, approvals, and change history across device and clinical documentation. +
Job description
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