Provides administrative support to the Product Disposition, Incoming Inspection and Quality Systems areas such as: review and control of incoming and outgoing correspondence, data entry, records keeping and filing, answering the phone and processing of work orders and purchasing orders. Prepares certificate of Compliance for approved lots. Makes photocopies of executed batch records. Coordinates training on procedures and batch records. Prepares Quality Metrics reports and lots verification schedule. Prepares and delivers the Approved Suppliers List. Assigns control number to investigations, change requests and commitments. Responsible to document all Quality required information in accordance with good documentation practices.
Bachelors of Science Degree in Natural Science. At least one (1) year of experience in the pharmaceutical industry including manufacturing processes, QNQC controls. Strong knowledge of regulatory requirements and computer literacy. Fully bilingual (Spanish/English).