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The Digital Product Owner will manage data visualization products, overseeing agile development, user research, and adoption strategies to enhance scientific productivity in drug discovery.

The Senior Nonclinical Statistician provides statistical support for preclinical research, collaborates with project managers, and ensures compliance with regulatory standards.

The Associate Scientist will design and conduct purification experiments, document results, evaluate technologies, and maintain knowledge in purification processes.

The Head of Toxicology Innovation leads strategies to integrate AI and ML into toxicology, oversees labs in France and the US, and ensures high-quality safety assessments in drug development.

The Quality Assurance Specialist ensures compliance with GMP, conducts audits, resolves quality issues, implements improvements, and fosters a quality culture.

The candidate will develop and validate analytical methods in a GMP environment for biotherapeutics, perform cell culture, and support testing and reporting tasks.

Design, develop, and maintain software applications for R&D, focusing on data quality and automation in laboratory environments. Collaborate with teams and support users.

The Thought Leader Liaison engages with healthcare professionals and KOLs to develop relationships and execute marketing strategies for rare blood disorders.

The Director will lead strategic PBM models and market access innovations while collaborating with various teams to drive patient-centered solutions and optimize market access.

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.