Innovate global CMC regulatory strategies and submissions for biological products. Ensure high-quality compliance with US and Canadian regulations, while collaborating cross-functionally to manage lifecycle changes effectively.

Champion the design and scale-up of injectable product processes, driving technology transfer in a GMP-compliant environment. Collaborate on projects, provide scientific support, and engage with clients for successful commercial outcomes.

Empower strategic product innovation and lifecycle management for scientific solutions. Collaborate cross-functionally to develop impactful product strategies and drive revenue growth, while leading global teams to exceed customer expectations.

Lead and optimize sterile manufacturing operations in a large multi-product facility, ensuring safety, quality, and cost efficiency while driving performance with strategic operational plans and cross-functional collaboration.

Empower continuous improvement through effective training and quality initiatives. Assist in developing and delivering programs while conducting quality reviews and supporting compliance with industry regulations.