GMP & Production Coordinator II (1st Shift)

RiseMe; Grand Rapids (MI); On-site; USD 65,000 - 82,000; Full time

Benefits offered by this job

Benefits starting day 1

Paid volunteerism starting day 1

Paid time off (PTO)

Wellness time off (WTO)

Paid holidays

Job summary

Grand River Aseptic Manufacturing (GRAM) in Grand Rapids, MI, seeks a Manufacturing Coordinator II to support sterile operations and coordinate customer manufacturing from documentation to packaging. This role emphasizes administrative and logistical tasks to back the production schedule and customer expectations, with primary location at the Butterworth facility on 1st shift.

You will interact with MSAT, QA, Supply Chain, and Validation teams to ensure compliance with cGMP and timely completion

Qualifications

• Bachelor’s degree or equivalent training and/or experience.
• Strong operational and tactical orientation.
• Proficient computer skills in Microsoft Word, Excel and Outlook.

Responsibilities

• Support the production schedule by ensuring materials are available and compliant with GRAM procedures.
• Maintain product quality, safety, and alignment with the production schedule.
• Prepare and review floor documentation including logs, forms, Master Batch Records, equipment reports, and work orders.
• Escalate issues to maintain forecasted production plans and address material shortages.
• Maintain accurate inventory counts using GRAM inventory management software.
• Coordinate with supervisors to evaluate methods for increasing efficiencies and maintain a clean 5S workspace.

Skills

Operational mindset

cGMP knowledge

Microsoft Word

Microsoft Excel

Microsoft Outlook

Education

Bachelor’s degree or equivalent training/experience

Tools

Microsoft Word

Microsoft Excel

Microsoft Outlook

Job description

Grand River Aseptic Manufacturing (GRAM) in Grand Rapids, MI, seeks a Manufacturing Coordinator II to support sterile operations and coordinate customer manufacturing from documentation to packaging. This role emphasizes administrative and logistical tasks to back the production schedule and customer expectations, with primary location at the Butterworth facility on 1st shift.

You will interact with MSAT, QA, Supply Chain, and Validation teams to ensure compliance with cGMP and timely completion