Finishing Supervisor, Parenteral Drug Manufacturing

Grand River Aseptic Manufacturing; Grand Rapids (MI); On-site; USD 70,000 - 95,000; Full time

Benefits offered by this job

Medical benefits starting day 1

401(k) with immediate vesting

Paid volunteer time (16 hours)

PTO up to 17 days/year

8 paid holidays per year

Shift differential for second/third

Job summary

Grand River Aseptic Manufacturing in Grand Rapids, MI seeks a Finishing Supervisor to oversee multi-finishing operations for parenteral liquids, ensuring all work aligns with cGMPs, SOPs, and batch records to meet production schedules.

The role requires 2–5 years in pharma/FDA-regulated environments, GMP knowledge, and the ability to train staff, document results, and maintain safety and quality in a fast-paced facility.

Qualifications

• 2–5 years of relevant pharma/FDA experience.
• Knowledge of GMP standards and CFR guidelines.
• Ability to supervise manual and automated processes in pharma/FDA environment.
• Proficient in Microsoft Word, Excel and Outlook.

Responsibilities

• Coordinate activities across 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 procedures, product inspection and cGMPs.
• Accurately document data and complete batch records.
• Assist in scheduling and maintenance of production equipment.
• Participate in client communications, problem solving, and project status updates.
• Perform routine performance assessments with direct reports.
• Define and uphold disciplinary actions for poor performance.

Skills

Pharma experience

GMP/CFR knowledge

Supervisory skills

MS Office (Word/Excel/Outlook)

Decision making

Communication

Education

Bachelor's degree in life sciences

Job description

Grand River Aseptic Manufacturing in Grand Rapids, MI seeks a Finishing Supervisor to oversee multi-finishing operations for parenteral liquids, ensuring all work aligns with cGMPs, SOPs, and batch records to meet production schedules.

The role requires 2–5 years in pharma/FDA-regulated environments, GMP knowledge, and the ability to train staff, document results, and maintain safety and quality in a fast-paced facility.