QualityAssuranceSupervisor

**QA Supervisor** **Position Summary** * **Work schedule: M-F 8am-5pm** * 100% based on-site in Philadelphia, PA Catalent’s 206,878-square-foot Philadelphia-area facility serves as the global Center of Excellence for Clinical Supply Packaging, offering GMP secondary packaging and clinical labeling services. The site provides manual to fully automated packaging solutions, including temperature-controlled options for sensitive products. Come and be part of a team that delivers industry-leading quality and innovation. The Quality Assurance department is responsible for ensuring compliance with quality system and product quality requirements defined by international regulations and corporate, network, and local standard operating procedures. The Quality Operations department supports this by providing oversight and guidance on matters affecting the quality system or product quality in daily operations. **The Role** * Responsible for all QA activities related to incoming, distribution and destruction and process auditing * Assist In ensuring the quality and identity of pharmaceutical products during all aspects of the incoming, distribution, or packaging processes * Act as the Quality partner to support the Supply Chain and Operations department * Enforce Catalent policy and regulatory requirements * Act as site subject matter expert for "Good Manufacturing Practices" and "Good Distribution Practices" * Work to schedule a daily resource plan to support Supply Chain/Operations activities * Act as lead investigator for all compliance issues regarding incoming, distribution, returns, destruction, or packaging/production * Develop process excellence and efficiencies prior to the beginning of a project * Track and report metrics and identify trends and predictive models * All other duties as assigned **The Candidate** * HS Diploma/GED and 5+ years of Production QA experience required. * College degree preferred (BA, BS) * Proven track record of monitoring/auditing quality and