Pharma Finishing Supervisor — Fast-Paced GMP Leader

Grand River Aseptic Manufacturing, Inc.; Grand Rapids (MI); On-site; USD 75,000 - 95,000; Full time

Benefits offered by this job

Medical benefits starting day 1

Paid volunteerism starting day 1

PTO up to 17 days per year

8 paid holidays per year

401(k) contributions vest immediately

Job summary

Grand River Aseptic Manufacturing, Inc. is seeking a Finishing Supervisor to oversee multi-finishing operations for parenteral liquid drug products and ensure compliance with cGMP, SOPs, and batch records.

The role focuses on delivering on-time production to meet schedules, while guiding teams and maintaining quality standards. Ideal candidates possess 2–5 years in pharma or FDA-regulated environments, with GMP and CFR knowledge, plus proficiency in MS Office.

Qualifications

• 2–5 years of experience in a pharmaceutical or FDA-regulated environment.
• Knowledge of GMP standards and CFR guidelines.
• Ability to supervise manual and automated processes in a pharma setting.
• Proficient in Word, Excel and Outlook.

Responsibilities

• Coordinate activities across operational departments.
• Ensure adequate supplies to meet production needs.
• Write and revise departmental procedures and batch records.
• Assist with training in procedures, product inspection and cGMPs.
• Document data accurately and complete batch records as needed.
• Assist in scheduling and maintenance of production equipment.
• Participate in client communications, problem solving, and project status updates.
• Conduct routine performance assessments with direct reports.
• Define and uphold disciplinary actions for underperformance.

Skills

GMP knowledge

CFR guidelines

Microsoft Word

Microsoft Excel

Microsoft Outlook

Decision making

Education

Bachelor's degree in life sciences or equivalent

Job description

Grand River Aseptic Manufacturing, Inc. is seeking a Finishing Supervisor to oversee multi-finishing operations for parenteral liquid drug products and ensure compliance with cGMP, SOPs, and batch records.

The role focuses on delivering on-time production to meet schedules, while guiding teams and maintaining quality standards. Ideal candidates possess 2–5 years in pharma or FDA-regulated environments, with GMP and CFR knowledge, plus proficiency in MS Office.