Paris Perry

At Merck, I maintain controlled quality records, support divisional and FDA audits, and use Veeva Vault to issue and retain critical documents for visibility and traceability.

I investigate vaccine product complaints and adverse events through batch-record reviews, test records, and physical inspections. I also perform SOP and procedure gap assessments, develop shipping protocols, and work with teams to resolve compliance issues.

Previously, at Octapharma Plasma, I performed quality-control reviews, investigated deviations and customer complaints, completed root cause analysis, and supported the release of shipments and supplies. At Merck through Eurofins, I drafted and approved SOPs, forms, job aids, and quality reports.

My pharmaceutical science background also includes genomics laboratory work at Labcorp, including DNA extraction, amplification, Illumina microarray testing, and Tecan automation equipment.