Teams at Grand River Aseptic Manufacturing, Inc.

Supports pharmaceutical business operations by translating demand forecasts into production plans, tracking batch release activities and customer commitments, maintaining planning tools and reports, coordinating cross-functional meetings, documenting action items, monitoring performance metrics, identifying scheduling conflicts and operational risks, and escalating issues. The role also assists with presentations, data accuracy, leadership reporting, and continuous improvement initiatives in a fully onsite manufacturing environment.

Owns and supports quality systems for a quality control analytical laboratory, including CAPA, investigations, deviations, change controls, OOS processes, training, LIMS administration, equipment lifecycle management, and laboratory projects. Serves as a QC subject matter expert, leads cross-functional deliverables, troubleshoots instruments and software methods, manages vendors, and mentors laboratory personnel.

Lead GRAM’s Quality Systems while overseeing aseptic manufacturing operations. Responsibilities include managing quality teams, authoring and reviewing cGMP documentation, investigating nonconformances, interpreting regulatory standards, supporting regulatory interactions, allocating resources, and driving continuous improvement in a regulated pharmaceutical manufacturing environment.