Victoria Murken

I’m a quality-focused Technical Engineer and Compliance Investigator with 5+ years of experience in FDA-regulated manufacturing environments. I specialize in process validation, CAPA, and regulatory compliance to support advanced cell-based therapies while keeping product integrity at the center of every decision.

At Minaris Regenerative Medicine (Nov 2019 - July 2025), I conducted root cause investigations and implemented corrective and preventive actions to drive sustained quality improvement. I documented, examined, and resolved quality deviations in compliance with established procedures and regulatory expectations, while maintaining audit readiness through ownership of SOPs, batch records, and controlled quality documentation systems.

I also use structured problem-solving tools—including 5 Whys and Fishbone diagrams—to identify underlying issues and prevent recurrence. Working within regulated settings, I apply aseptic techniques, cleanroom operations, and cell handling protocols to support dependable, compliant manufacturing.

Earlier, as an Assistant Quality Laboratory Technician at Acupac Packaging Inc (Mar 2016 - Nov 2019), I supported compliance and product quality across FDA-regulated, OTC cosmetic, and industrial operations. From Good Documentation Practices to environmental monitoring (air sampling, DI water testing, and equipment swab collection), I contributed to cGMP adherence through careful testing, clear documentation, and quality-first execution.