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Lead the AI Methods group within AICS, manage AI researchers, ensure robustness of AI models, and foster collaborations for drug discovery advancements.

The Associate Director, Access & Reimbursement leads educational initiatives for account executives on access and reimbursement strategies while managing relationships with complex health systems, ensuring patient access to Novartis products through effective collaboration and problem-solving.

The Manufacturing Support Manager oversees the Critical Environment Cleaning Program, scheduling manufacturing activities, managing compliance, and leading projects and staff in a GMP environment.

The Senior Validation Engineer leads the qualification of equipment and processes, manages projects, and ensures compliance with regulatory standards, while mentoring team members.

The Downstream Manager oversees manufacturing operations, ensuring compliance with GMPs, leading teams, and managing production processes while driving continuous improvement initiatives.

The RD Associate Director develops and implements regulatory strategies for precision diagnostics, ensuring compliance with IVD regulations and supporting submissions for clinical trials and diagnostic products.

The Validation Engineer II is responsible for managing validation and qualification activities, drafting documents, and ensuring compliance with cGMP regulations.

The Global Program Clinical Head leads clinical programs ensuring compliance with regulatory requirements and guiding strategic clinical development decisions while collaborating with various stakeholders.

Lead global project teams through the proof-of-concept phase of drug development, oversee clinical studies, and collaborate on strategies for clinical and preclinical development.

The Manufacturing Operations Specialist manages inventory, supports manufacturing procedures, ensures compliance, and maintains accurate records in a cGMP-regulated environment.