GxP Compliance & Digital Data Quality Lead

A leading biopharmaceutical company based in Wilmington, Delaware, seeks an experienced IT compliance professional to ensure regulatory adherence and quality in pharmaceutical manufacturing systems. The role requires a minimum of 5 years in the regulated pharmaceutical industry, strong knowledge of FDA and EU regulations, along with project management skills. Responsibilities include reviewing validation documentation, supporting audits, and driving compliance initiatives within the organization. Excellent communication and problem-solving skills are essential, as well as the ability to collaborate effectively across diverse teams.
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