Teams at Grand River Aseptic Manufacturing, Inc.

The QA Specialist ensures compliance in manufacturing processes, oversees quality systems, performs batch record reviews, and collaborates on quality investigations.

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.

Manage bi-weekly payroll processing and benefits administration: process enrollments and changes, reconcile benefits invoices, support 401(k) administration, maintain HRIS and payroll records, assist employees with payroll and benefits questions, and provide administrative HR support.