Join our team to develop scientific content that advances communication strategies across innovative platform and pipeline programs while collaborating with cross-functional stakeholders to achieve scientific goals.

Develop strategic supplier relationships to optimize procurement processes, manage high-value material orders, and ensure timely delivery while adhering to compliance standards. Utilize analytical skills to drive continuous improvement in supply chain operations.

Drive product validation activities for injectable assets, ensure GMP supply, and author regulatory documents, while collaborating across teams to meet clinical trial timelines and maintain high standards in pharmaceutical development.

Join a team that's pivotal in managing GxP computerized systems, ensuring compliance, validation, and data integrity through effective collaboration with Quality Assurance and Regulatory Affairs. Drive impactful projects and solutions across the lifecycle.

Shape the future of preclinical safety assessment by leading studies, evaluating toxicology results, and guiding regulatory strategies for novel therapeutic oligonucleotides aimed at rare diseases, ensuring compliance and scientific excellence.