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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.

Summer Corporate Communications intern supporting internal and external communications across R&D and commercial functions. Duties include drafting/editing intranet content, newsletters, press materials, social media support, industry/media research, and event communications. Internship includes trainings and leadership engagement, running June 1–August 10, 2026.

The Associate Director will oversee quality operations, drive efficiency, manage risks, ensure compliance, and lead process improvement initiatives in a global quality organization.

The Director is responsible for developing and overseeing global engagement strategies with external stakeholders, ensuring effective communication and governance across functions.

The Director of Global Quality GMP Processes leads the optimization of quality processes, ensuring compliance with GMP and regulatory standards, and promotes continuous improvement in product quality across regions.

The Associate Director is responsible for overseeing global labeling processes, ensuring compliance, collaborating with teams, and managing documentation for drug products.

The Manager, Global Product Quality oversees compliance with GMP and DEA regulations for controlled substances, ensuring quality and regulatory oversight throughout the product lifecycle and collaborating with cross-functional teams.

The Executive Director will lead U.S. Pricing and Contracting, develop long-term strategies for pricing, governance, and GTN performance, ensuring compliance and integration into portfolio management.