Lead execution of CapEx projects from feasibility to start-up; ensure project quality, adherence to budget and schedule while collaborating with internal teams and external contractors, guaranteeing technical excellence throughout the project lifecycle.

Lead the Document Control team to enhance quality operations, ensuring compliance and efficient management of controlled documents while supporting cross-functional collaboration and continuous improvement in a GMP-regulated environment.

Lead Quality Control efforts while advancing testing methods for gene therapy products. Oversee a dynamic team and ensure compliance with cGMP standards. Drive continuous improvement in laboratory processes and mentor junior scientists.

Transform downstream manufacturing operations by leading a skilled team in the purification of viral vectors for gene therapy. Oversee GMP practices, optimize processes, and collaborate across functions to deliver high-quality client projects efficiently.