Lead the charge in ensuring patient safety by providing expert medical oversight in pharmacovigilance efforts, analyzing safety data, and collaborating across teams to guide regulatory strategies for innovative therapies that shape drug development.

Grow your career with our team as a Senior Scientist in Analytical Development. Leverage your expertise in drug product analytical methods, supporting regulatory submissions and guiding cross-functional projects to drive innovative oncology solutions.

Take ownership of analytical method development and material characterization, ensuring compliance with cGMP standards. Collaborate across departments, manage reference standards, and leverage mass spectrometry to enhance drug development processes.

Champion the regulatory writing team to ensure high-quality submissions and timelines. Lead internal and external medical writers for clinical documents, navigating cross-functional collaborations in oncology clinical research.

Shape the future of computer systems assurance by leading risk-based validation strategies in a fast-paced biotech environment. Drive compliance and optimization for GxP systems, ensuring regulatory alignment and operational excellence.