Transform synthetic processes for critical API manufacturing, leading cross-functional teams to ensure successful scale-up and tech transfer in a cGMP environment. Drive innovation and compliance from development to regulatory readiness.

Unlock potential by leading the development of innovative synthetic processes for critical APIs. Collaborate with cross-functional teams and external partners to ensure successful scale-up and commercialization in a cGMP environment.

Lead and execute the GCP Quality strategy for clinical development, ensuring compliance and high-quality oversight. Engage cross-functional teams to drive risk management and inspection readiness while championing a culture of accountability and excellence.

Advance your career by providing strategic leadership in Product Quality management. Drive compliance, oversee manufacturing processes, and partner cross-functionally to ensure successful BLA submissions and commercialization in a dynamic biotech environment.

Shape the future of ocular oncology by overseeing Trial Master Files, ensuring compliance and quality across clinical trials while collaborating with cross-functional teams and leading TMF governance initiatives.