Associate Director, Quality

This is where  your work makes a difference. At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond. Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results. Here, you will find more than just a job—you will find purpose and pride.

This position is responsible for being Most Senior plant level Quality Management Representative, developing and deploying the quality system for the plant, assuring systems and procedures for regulatory compliance are established and deployed What You'll Be Doing Serve as the Management Representative for Quality and lead the Quality organization within a mid-to-large manufacturing facility. Build and develop a high-performing Quality organization with a clear vision and mission that supports business growth and global expansion. Oversee batch review and product release activities. Fulfill the responsibilities of the Person Responsible for Regulatory Compliance (PRRC), including ensuring device conformity is appropriately verified in accordance with the Quality Management System before release. Ensure Post-Market Surveillance (PMS) obligations are fulfilled. Ensure vigilance reporting requirements are met in accordance with Articles 87-91 of the Medical Device Regulation (MDR). Direct large-scale programs and departmental initiatives in support of division-wide and company-wide objectives. Maintain accountability for product quality, regulatory compliance, and adherence to Baxter quality policies. Develop, implement, and maintain quality systems, including Management Review, CAPA, Design Controls, and Process Controls, to ensure products meet defined requirements. Ensure compliance with applicable regulatory requirements and manage regulatory inspections and audits. Conduct periodic reviews of the Quality Management System with executive leadership to ensure effectiveness and continued suitability. Drive continuous improvement initiatives across processes and systems while supporting deployment of divisional and corporate quality programs. Assess and advise senior leadership on quality-related aspects of acquisition targets. Collaborate effectively with stakeholders across functions, business units, and global locations. Serve as the primary quality representative in interactions with customers and regulatory agencies regarding products, systems, and processes. Ensure adherence to established specifications, procedures, and standards supporting product quality and regulatory compliance. Develop and manage the Quality organization budget and ensure effective utilization of departmental resources. Lead coaching, training, performance management, employee development, and succession planning initiatives for the Quality team.

In-depth knowledge of the regulatory environment governing the manufacture of medical devices and therapeutics. Proven leadership experience managing large teams in a complex, regulated environment. Demonstrated ability to lead within a matrix organization and collaborate effectively across global, cross-functional teams. Strong analytical, problem-solving, and decision-making skills. Excellent verbal and written communication skills. Proven success working with multifunctional and global teams. Strong interpersonal, influencing, and negotiation skills. Extensive knowledge of applicable quality systems, regulatory standards, and industry regulations. Experience in risk management, validation, analytics, and