Patricia Galvez

Maintained and organized controlled documents, procedures, and quality records using a document management system. Reviewed records for completeness, accuracy, and compliance, and supported audits and process improvements.

Reviewed medical records and extracted relevant information according to detailed criteria. Entered, validated, and maintained clinical data while performing quality checks and resolving discrepancies.

Maintained and reviewed clinical research documents and study information for completeness and accuracy. Performed source document review, data verification, and query follow-up using electronic systems.

Maintained inventory records and monitored supplies using organized tracking systems. Prepared and maintained documentation related to inventory, distribution, and daily operations.

Maintained controlled documents, master lists, records, and trackers for company procedures and production documents. Reviewed documents for accuracy, completeness, and compliance, and coordinated updates across functions.

Recorded, reviewed, and maintained analytical data and laboratory documentation. Performed data checks and investigated discrepancies in test results and records.

Currently in progress: ISO 13485:2016 Foundational Course.

Completed PIC/S GMP Training from the Food and Drug Administration in August 2025.

Completed ISO 9001:2015 Quality Management System Internal Auditor training in November 2025.

Completed Lean Six Sigma Yellow Belt certification in December 2025.

Completed GMP of Medical Gases and FMEA Risk Assessment and Validation for Medical Gases training in October 2025.

Registered Pharmacist (RPh) credential obtained from the Professional Regulation Commission in August 2018.

Bachelor of Science in Pharmacy degree from Saint Louis University, completed in May 2018.