Quality Associate III - Doc Center

Your role as a Quality Associate III-Doc Center positions you to be directly involved in the physical production that enables Baxter to fulfill our mission to save and sustain lives. You manage the line between meeting production timelines and making quality products. As a manager, you are the trusted critical connection between the business and the workers on the floor. Lead ongoing daily departmental activities for areas of direct responsibility and assist other Quality areas in the successful performance of these activities. Manage activities of self in achieving defined quality goals in an efficient, accurate and timely manner. Ensure business needs and timeliness requirements of the department are met or exceeded globally. Write, review, analyze and revise written Procedures and submit procedural changes as needed to meet Corporate, Divisional, Plant, Regulatory Requirements, etc. Partners with facilities, divisions, and regions to ensure successful implementation and compliance to procedures / regulations. Be involved in and lead multiple process/product improvement projects or other focus groups, design of experiments, validations, development of new methodologies and improving existing methodologies, data generation, report development and presentation. Lead audit ready status efforts for assigned areas and assist other areas within the facility in understanding FDA, ISO and Baxter quality requirements. Maintain a high level of expertise in current regulatory requirements.