The Process Engineer will develop specifications for systems in biopharmaceutical manufacturing. Responsibilities include designing cleanrooms, overseeing compliance with FDA regulations, executing Factory Acceptance Testing, and supporting production optimization. Additionally, the engineer will coordinate projects with clients and assist in manufacturing troubleshooting and improvements.

The Senior Associate in Upstream MSAT is a technical expert responsible for managing upstream process manufacturing for biopharmaceuticals. Key duties include designing and implementing manufacturing processes, creating GMP documents, overseeing technical operations, and providing training to staff. The role also involves continuous process improvement and compliance with quality standards.