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The Associate Director will optimize GMP processes, lead cross-functional quality initiatives, ensure compliance, and enhance quality system performance globally.

The Director leads market access strategies, developing value propositions, managing payer marketing, and collaborating with brand teams to drive initiatives while managing resources and engaging stakeholders.

The Associate Director will develop and implement strategic plans, oversee operations, improve processes, manage budgets, and collaborate across functions in Global Medical Affairs.

The Senior Manager will oversee strategic initiatives for Medical Affairs, focusing on external stakeholder engagement and cross-functional collaboration. Responsibilities include strategic planning, developing engagement models, and ensuring compliance with regulations.

The Senior Manager oversees quality assurance for biologics manufacturing, ensuring compliance with GMP standards, managing contract manufacturers, and leading quality system records for clinical and commercial products.

The Director, Global Training leads the development of global training strategies for non-GxP curricula, ensuring compliance and continuous improvement in organizational learning programs and stakeholder engagement.

Lead the global GxP training strategy, oversee training program development and compliance, and ensure adherence to regulatory standards within the pharmaceutical industry.

The Senior Director of Global Quality Solutions drives efficiency in quality processes through automation, leading digital transformation initiatives, managing projects, and fostering innovation in document management.

Oversee global training operations ensuring compliance and efficiency, manage systems, collaborate with stakeholders, and lead improvement initiatives.

The Senior Director will lead the establishment of a global learning and development center focusing on GxP compliance and training initiatives, driving innovation and efficiency.