Tina Andersen is an experienced Quality Assurance professional with over 20 years in the Medical Device and Pharmaceutical sectors. They have served in significant roles, including VP Quality and Regulatory Affairs at DDD-Diagnostic A/S and are currently a Senior QA and QMS Specialist at Axlab, where they focus on implementing ISO13485 and IVDR compliance. Tina has hosted numerous inspections and successfully led audits, contributing to organizations’ compliance with complex regulatory frameworks. Their educational background includes a B.Sc. in Engineering Chemistry and a Lead Auditor certification.
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