Unlock potential by leading lipid process chemistry for GMP manufacturing, overseeing development and scale-up of novel lipid components. Collaborate with CDMOs and cross-functional teams to ensure regulatory compliance and product quality.

Lead the charge in advancing clinical development for gene-editing therapeutics, focusing on early-stage studies. Collaborate with cross-functional teams to design and execute global trials, ensuring high-quality outcomes and regulatory compliance.

Unlock potential by leading global regulatory strategy for innovative gene editing therapies. Drive submissions, engage with health authorities, and shape evidence generation in a fast-paced biotech environment, ensuring compliance and strategic alignment.

Transform quality systems by enhancing compliance, managing documentation, and supporting vendor activities in a collaborative QA team focused on clinical candidates. Contribute to process improvements and ensure optimal performance.

Lead strategic medical affairs initiatives, engaging cross-functional teams and external stakeholders to advance innovative therapies through clinical phases while ensuring compliance and scientific integrity in communications.