Teams at Grand River Aseptic Manufacturing, Inc.

Provide technical support for GMP pharmaceutical manufacturing across multi-product CDMO sites. Lead deviation investigations, root cause analysis, CAPA, author procedures, support validation/commissioning, monitor process data, and collaborate cross-functionally to drive continuous improvement and ensure compliance.

Execute technical support for GMP manufacturing operations in a formulation and aseptic fill/fill-finish facility. Responsibilities include change control and corrective-action projects, cGMP discrepancy resolution, batch data analysis, equipment troubleshooting, preventive maintenance, process optimization, SOP updates, cleanroom and utility upgrades, validation support, and collaboration across manufacturing, quality, engineering, microbiology, and project teams. Weekend production coverage, off-shift availability, and occasional on-call support are required.

Manage bi-weekly payroll and benefits administration: process timecards and payroll changes, enroll and support employees in benefits and 401(k), reconcile benefits invoices, maintain HRIS records, assist with leave claims and verifications, provide employee support, and offer administrative HR assistance onsite.