Manufacturing Operations Coordinator II - GMP & Scheduling

Grand River Aseptic Manufacturing Inc.; Grand Rapids (MI); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Benefits starting day 1

401(k) vesting

Volunteer time

PTO + WTO

Paid holidays

Competitive pay

Job summary

Grand River Aseptic Manufacturing seeks a Manufacturing Coordinator II to support sterile operations and coordinate the customer manufacturing process from documentation to packaging. The role is based at the Butterworth facility, on 1st shift, and includes administrative duties to back the production schedule and meet customer expectations.

The position requires a bachelor’s degree or equivalent, strong computer skills (Word, Excel, Outlook), and knowledge of cGMP/regulatory standards.

Qualifications

• Bachelor's degree or equivalent training and/or experience.
• Strong operational and tactical orientation.
• Thorough understanding of cGMP, FDA/EMA guidelines and multinational regulatory standards.
• Proficient computer skills: Word, Excel, Outlook.

Responsibilities

• Support production schedule by ensuring materials are available and compliant with GRAM procedures.
• Maintain product quality, schedule, and safety guidelines on the floor.
• Prepare and review Master Batch Records, logs, forms, equipment reports and work orders.
• Escalate shortages to maintain forecasted production plans and inventory counts in GRAM systems.
• Coordinate and track logistics of equipment (dedicated, support, non-dedicated).
• Interface with MSAT, Quality Assurance, Supply Chain, and Validation to support the production floor.

Skills

Operational orientation

Education

Bachelor's degree or equivalent

Tools

MS Word

Excel

Outlook

Job description

Grand River Aseptic Manufacturing seeks a Manufacturing Coordinator II to support sterile operations and coordinate the customer manufacturing process from documentation to packaging. The role is based at the Butterworth facility, on 1st shift, and includes administrative duties to back the production schedule and meet customer expectations.

The position requires a bachelor’s degree or equivalent, strong computer skills (Word, Excel, Outlook), and knowledge of cGMP/regulatory standards.