Own the analytical characterization of raw materials in biologics manufacturing. Collaborate cross-functionally to assess risks, ensure product quality, and maintain supply continuity with a focus on innovative solutions to variability challenges.

Join a team that's pivotal in managing global regulatory affairs and clinical safety for business development deals. You'll oversee due diligence, contract negotiations, and cross-functional coordination to ensure successful deal execution and alliance management.

Pioneer impactful business development initiatives by leading GRACS activities, guiding due diligence processes, contract negotiations, and driving cross-functional project teams to ensure seamless execution and management of strategic partnerships.

Develop and validate statistical programs for clinical data analysis, collaborating with cross-functional teams to produce high-quality outputs that adhere to industry and regulatory standards throughout the project lifecycle.

Take ownership of maintenance and calibration services for production lab equipment, ensuring compliance and operational efficiency. Collaborate with cross-functional teams to enhance performance in a regulated manufacturing environment.