Teams at Grand River Aseptic Manufacturing, Inc.

Lead end-to-end technology transfer, commercial supply, and lifecycle management projects for sterile pharmaceutical manufacturing. Act as primary customer liaison, define scope and schedules, manage risks and change control, maintain project documentation in SmartSheet, coordinate cross-functional teams, and support customer visits while driving issue resolution and process improvements.

Support GMP manufacturing in a multi-product aseptic fill/finish CMO: troubleshoot and optimize processes, execute change control and CAPA actions, analyze batch data, maintain equipment, update SOPs, assist with PMs and cleanroom/utility upgrades, and collaborate across QA, MSAT, validation, and operations.

The Director of Manufacturing will oversee production management, continuous improvement, capability building, and people management, ensuring quality and operational excellence in compliance with regulations.