Pharma Finishing Supervisor — cGMP, Fast-Paced Ops

Grand River Aseptic Manufacturing Inc.; Grand Rapids, Northern (MI, KY); Hybrid; USD 70,000 - 95,000; Full time

Benefits offered by this job

Medical benefits starting day 1

401(k) program with company matching

Paid volunteerism starting day 1

PTO up to 17 days/year

8 paid holidays/year

Shift differential

Job summary

Grand River Aseptic Manufacturing Inc. (GRAM) seeks a Finishing Supervisor to oversee multi-finishing operations of parenteral liquid drug products, ensuring compliance with cGMPs, SOPs, batch records, and labor and material standards while meeting the forecasted production schedule.

The role requires 2–5 years in a pharmaceutical or FDA-regulated environment, GMP knowledge, and ability to supervise both manual and automated processes.

Qualifications

• Two to five years of relevant experience in pharmaceutical or FDA regulated industry.
• Knowledge of GMP standards and CFR guidelines.
• Technical skills to supervise manual and automated processes in a pharmaceutical or FDA regulated environment.
• Ability to make informed decisions.
• Proficient with Word, Excel and Outlook.

Responsibilities

• Coordinate activities by communicating with other operational departments.
• Ensure adequate levels of operating supplies to meet production needs.
• Write and/or revise departmental procedures and batch records.
• Assist with training employees in all departmental procedures, product inspection and cGMPs.
• Accurately document data and complete batch records as needed.
• Assist in scheduling and performance of routine maintenance of production equipment.
• Participate in client communications, including problem solving, schedule development, and project status updates.
• Perform routine performance assessments with direct reports.
• Define and uphold disciplinary actions for poor performance of direct reports.

Skills

Decision making

Attention to detail

Problem solving

Communication

Education

Bachelor's degree in life sciences

1+ year experience as inspector of parenteral products

Tools

Microsoft Word

Excel

Outlook

Job description

Grand River Aseptic Manufacturing Inc. (GRAM) seeks a Finishing Supervisor to oversee multi-finishing operations of parenteral liquid drug products, ensuring compliance with cGMPs, SOPs, batch records, and labor and material standards while meeting the forecasted production schedule.

The role requires 2–5 years in a pharmaceutical or FDA-regulated environment, GMP knowledge, and ability to supervise both manual and automated processes.