This individual will be a part of a team which will implement, support and maintain pharmaceutical cGMP’s and the Quality Management System at the Madison site as needed to assure the compliance of products produced by DuPont with all internal, customer and regulatory requirements.Essential Duties and Responsibilities•  Contribute to the review and assessment of Deviations, Management of Change, Corrective Actions, and Non-Conformances.•  Participate in the review and approval of validation documentation.•  Participate in customer, certification, and regulatory audits and following up on corrective actions, as needed.•  Contribute to monitoring and trending of process performance for APR (Annual Product Review) and plant continuous improvement initiatives.