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The CMC Project Leader manages pre-clinical and early clinical development projects, leading cross-functional teams to ensure alignment and execution of CMC activities. Responsibilities include project strategy, budget management, risk assessment, and regulatory submissions.

The Syringe Process Manager oversees shift operations, drives continuous improvement, manages personnel, ensures compliance with regulations, and develops team capabilities.

The Hospital Business Manager will drive sales performance, engage hospital healthcare professionals, and support products' clinical education within Hospital Account sales teams, focusing on enhancing vaccination efforts.

The Director oversees US Advertising and Promotion in Global Regulatory Affairs, ensuring compliance with regulations and managing strategic directions for product promotion and labeling.

The Statistical Project Leader oversees statistical contributions to clinical studies, ensuring quality and compliance, while mentoring team members and collaborating across functions.

Lead regulatory review and guidance for advertising, promotion, and labeling for immuno-oncology products. Serve as RC regulatory representative, collaborate with commercial, medical, legal, and compliance teams, liaise with FDA (OPDP/APLB), train staff, and ensure promotional materials meet federal regulations and corporate policies.

This role is an apprenticeship in QC Lab where you will learn about quality control processes, laboratory practices, and analytical techniques while working and studying.

The Head of PPA, External Data and AI Workflows will lead strategy and product management for analytics and external data sharing, integrating AI in R&D, and managing high-impact domains.

The Strategic Account Manager educates stakeholders on Tzield administration, develops account-specific strategies, and collaborates with teams to enhance patient care.

The Quality Third Party Management Specialist ensures third-party quality compliance, manages quality agreements, collaborates on investigations, and interprets regulations in the biotech industry.