Quality Assurance Specialist
Currento Experienced in performing in-process and final product reviews of documents to ensure adherence to accurate format, signatures, dating, and Good Documentation Practices (GMP) for both commercial and clinical products.o Review 25-30 shipping documents a day/night to ensure accurate order shipment.o Works closely with Research & Development, Regulatory Affairs, Clinical, and Manufacturing groups to determine determine the readiness of inspected products for shipment.o Collaborates closely with Research & Development, Regulatory Affairs, Clinical, and Manufacturing teams to determine the readiness of inspected products for shipment. Demonstrates proficiency in basic computer operations, utilizing Microsoft Word and Excel to generate reports and graphso Ensures compliance with operating procedures and completion of requisite training prior to task execution, maintaining adherence to current Good Manufacturing Practices (GMP). Diligently reviews shipping documentation to assure the accuracy of order shipments."