Champion quality control initiatives by overseeing testing programs for raw materials, ensuring compliance with industry standards, and collaborating with cross-functional teams to maintain production schedules and quality assurance.

Support and enhance laboratory operations through effective execution of upstream and downstream processes, ensuring compliance with Good Manufacturing Practices while collaborating in a cross-functional team environment to meet project objectives.

Elevate quality assurance by supporting GXP activities and enhancing Quality Systems. Collaborate across functions to ensure compliance with cGMP and improve document management processes for an audit-ready environment.

Champion drug product process development by leading characterization studies, optimizing GMP workflows, and collaborating with cross-functional teams to enhance commercialization readiness and regulatory compliance in biologics manufacturing.