Lead and transform analytical development and quality control, overseeing strategies for product lifecycle management, ensuring compliance, and fostering innovation while managing high-performing teams and external partnerships.

Lead a team that's committed to advancing global medical writing for critical clinical and regulatory documents. Collaborate with cross-functional experts to deliver precise, high-quality submissions that enable breakthrough therapies for rare diseases.

Grow your expertise in GCP as you manage compliance for clinical studies, support regulatory inspections, and oversee quality assurance processes. Collaborate with cross-functional teams to enhance efficiency and uphold high-quality standards.

Drive nonclinical development strategies, ensuring high-quality toxicology and DMPK oversight from IND-enabling to late clinical stages. Collaborate cross-functionally and provide scientific leadership to support regulatory submissions and decision-making.

Architect innovative drug-device combination products, leading their development and lifecycle management from concept to commercialization, while ensuring compliance and patient-centric design in injectable delivery systems.