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The Senior Manager, Global Procurement is responsible for CMO category strategy, supplier management, negotiations, and process improvements in procurement for advanced therapies within the biopharmaceutical industry.

The Associate Director, Government Pricing oversees compliance with pricing regulations, including submitting reports, analyzing pricing trends, and communicating with internal teams. Responsibilities also include monitoring pricing legislation and performing detailed calculations to ensure accurate submissions to government agencies.

The Director of Resource Management oversees strategic resource planning and management in research and development, ensuring efficient utilization of resources and leading a team of resource managers.

The Sr. Device Development Engineer leads multidisciplinary teams in developing device combination products, focusing on product management, regulatory compliance, and cross-functional collaboration.

Lead and oversee clinical data management across therapeutic areas, supervise and mentor data managers, ensure database design, validation, and archival meet SOPs and regulations, coordinate with clinical teams and CROs, and drive data quality, outsourcing strategy, and documentation.

The Senior Scientist will utilize AI for biomolecule design and optimization, collaborating cross-functionally to enhance therapeutic development using generative AI technologies.

The Associate Director, Thought Leader Liaison for Neurology will implement strategic engagements with key thought leaders, coordinating insights and discussions related to medical information and company products while ensuring compliance with industry regulations.

The Senior Manager, Regulatory Affairs will oversee advertising and promotion regulations for marketed products, collaborating with cross-functional teams to ensure compliance and provide strategic regulatory advice.

This role involves developing and optimizing data models for clinical data, ensuring compliance, leading automation processes, and mentoring a cross-functional team to enhance data quality and architectural performance.

The Senior Project Engineer will lead design, specify equipment, manage projects, support QA, develop documentation, and supervise contractors in biopharmaceutical process engineering.