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The role involves designing, developing, and maintaining data integration solutions across enterprise systems while ensuring compliance and performance. Responsibilities include monitoring EDI interfaces, collaborating with stakeholders, and optimizing integration workflows.

The Senior Manager, CMC Regulatory Affairs oversees CMC submissions and regulatory compliance for pharmaceutical products, manages multiple projects, and guides teams on regulatory strategies and documentation readiness.

This role involves executing bioassay testing, ensuring compliance with regulatory standards, overseeing testing operations, mentoring staff, and participating in method development.

The GxP Endpoint Engineer manages the SCCM environment for compliance in GxP operations, overseeing deployments, patch management, and QA processes while creating documentation and collaborating with various teams.

The Principal Scientist will lead AI-enabled design of antibodies, mentor designers and develop computational frameworks for protein design, driving multiple projects in parallel.

Manage planning processes for the Clayton manufacturing site, optimize production plans, oversee supply chain operations, and ensure efficiency in mRNA medicine production.

Lead the Quality Control Operations group, ensuring compliance and enhancing laboratory systems through digital transformation and data integrity. Oversee QC processes and collaborate with QA, IT, and automation teams.

The attorney will oversee IP litigation strategy, manage a docket of U.S. litigation matters, and coordinate with various teams for proactive disclosures and risk management.

The Vice President, HRBP will strategize and deliver people strategies, partner with executives, and lead workforce transformations leveraging AI and data-driven insights.

Design, develop, and deliver data integration solutions for manufacturing systems, ensuring high availability and performance while supporting operational tasks 24/7.