Lead the charge in technical oversight of small molecule API development and manufacturing to drive successful product milestones and support lifecycle management. Collaborate cross-functionally to ensure quality and compliance throughout development.

Join us to lead analytical method development and validation in a dynamic environment, ensuring compliance with cGMP and regulatory standards for rare disease drug products, while collaborating across technical teams for optimal project success.

Shape organizational growth and operational effectiveness by leading strategic initiatives and change management across functions to enhance performance and culture in a rapidly evolving company focused on rare diseases.

Take ownership of analytical method development, validation, and transfer for drug substances/products. Collaborate across teams to ensure compliance with cGMP and regulatory standards while leading technical initiatives in a virtual environment.

Transform the organization by leading enterprise effectiveness initiatives, driving strategic execution, and enhancing operational capabilities. Collaborate across functions to foster a culture of agility and excellence while navigating growth issues.