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The Senior Associate Scientist will develop purification processes for drug development programs, plan and execute experiments, and ensure compliance with safety and regulatory standards.

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

Develop and apply multiscale computational models for complex diseases, ensure alignment with project team needs, and communicate modeling predictions to stakeholders.

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.

Lead a small molecular biology team to support upstream process development and baculovirus seed generation. Perform cloning, PCR, sequencing and bioinformatics, design and document experiments, support tech transfer and manufacturing, ensure compliance with SOPs, and collaborate with QC/QA/Regulatory teams.

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.