As a Third Party Management Specialist, you will ensure the quality and compliance of our pharmaceutical third-party partnerships by evaluating, qualifying, and certifying suppliers based on their quality systems and capabilities. You will develop quality agreements, establish audit programs to assess GMP/GDP compliance, and drive continuous improvement initiatives while identifying and mitigating risks. Your role involves resolving quality issues, managing corrective actions, and maintaining proper documentation of all third-party activities. Success requires experience in pharmaceutical quality management systems, strong analytical and communication skills, audit expertise, and project management capabilities to oversee multiple quality initiatives while ensuring regulatory excellence and patient safety. We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.