Posted:1 month ago|
Platform:
Work from Office
Full Time
Role & responsibilities Expertise in Quality Management System (QMS) implementation and continuous improvement initiatives Strong background in Quality Control (QC) and Quality Assurance (QA) across manufacturing and regulatory environments Hands-on experience in Validation processes , including equipment, process, and product validation In-depth knowledge of ISO 13485 standards and Audit Management , including internal, external, and regulatory audits
Newtech Medical Devices
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