2nd Shift Packaging Supervisor - Lead a 30-50 Team

RXinsider LTD.; Grand Island (NE); On-site; USD 74,000 - 103,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision coverage

Life insurance

Disability insurance

401K with company contribution

Wellness program

Job summary

Fresenius Kabi in Grand Island, NE seeks a Production/Inspection Supervisor to oversee 30–50 staff on the inspection and packaging lines. You will uphold cGMP/SOP standards, review batch records, and ensure accurate documentation while coordinating production schedules and payroll.

The role emphasizes safety, quality, and efficiency with a focus on timely training and continuous improvement. Strong communication and FDA-regulated industry experience are preferred.

Qualifications

• BS/BA preferred; work experience in lieu of degree possible.
• Previous supervisory experience in a production/manufacturing environment preferred.
• Proven oral and written communication and proofreading skills required.
• Detail oriented and proficient with computer tools: MS Office (Excel, Word, Access).
• Experience in an FDA regulated industry preferred (3–5 years).

Responsibilities

• Supervise 30–50 employees on Inspection and Packaging lines.
• Coordinate execution of production schedules based on customer demand.
• Ensure compliance with SOPs and cGMPs; review batch records and documentation.
• Complete all batch-related documents according to site release standards.
• Maintain payroll and oversee staff development and training.
• Write investigation reports for inspection/packaging issues.
• Perform SAP/EWM/OER transactions and update SOPs.

Skills

Supervisory experience

Oral and written communication

Detail oriented

Proficient in MS Office

Proofreading

Education

BS/BA degree

Tools

Excel

Word

Access

Job description

Fresenius Kabi in Grand Island, NE seeks a Production/Inspection Supervisor to oversee 30–50 staff on the inspection and packaging lines. You will uphold cGMP/SOP standards, review batch records, and ensure accurate documentation while coordinating production schedules and payroll.

The role emphasizes safety, quality, and efficiency with a focus on timely training and continuous improvement. Strong communication and FDA-regulated industry experience are preferred.