Teams at Grand River Aseptic Manufacturing, Inc.

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

Supervise aseptic manufacturing operations in a cGMP sterile filling facility: lead staff, oversee cleanroom operations, ensure documentation and compliance, support continuous improvement, and manage deviations and client communications.

Manage and oversee quality systems for cGMP drug manufacturing (NCR, CAPA, Change Control, EV). Lead investigations, facilitate cross-functional teams, implement quality deliverables, own processes, and train staff on root cause analysis and quality system best practices.