Responsible for managing all aspects (i.e. quality systems, release, documentation, laboratory operations, compliance, training, staffing and budgetary needs, etc.) of the Quality Assurance Fractionation Business Unit. In addition to the duties described above the QA Manager provides QA support of NFF and NFB pooling and fractionation processes. These processes include pool record review and release, shipment of pool samples to EU regulatory authorities for testing and approvals, review and release of intermediate shipments to contract customers as well as intermediate shipment receipts from other Grifols manufacturers. Responsibilities may include roles such as document author/reviewer or approver in the administration of quality systems such as Change Control, Discrepancy Management, Intermediate Quarantine, pool and fractionation Batch Record review, documentation, SAP Master Data, and Annual Product Reviews as well as provide Quality input for validation projects, capital engineering projects, clinical studies, stability studies, ETPs, and Regulatory submissions. Responsible for representing QA Fractionation at manufacturing business unit meetings, and project meetings. Excellent communication skills (written and verbal) and extensive working knowledge of applicable regulations (i.e. U.S. Food and Drug Administration, Eudralex, Health Canada) and other applicable regulatory agency requirements/guidelines. Ability to perform methodical, risk-based analysis of situations and propose improvements. Good organizational skills are a must and ability to follow up on items to completion in a timely manner.
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Job Type
Full-time
Career Level
Manager
Education Level
Ph.D. or professional degree
Number of Employees
101-250 employees