Night Shift Production Supervisor – Process & Quality Lead

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

Benefits offered by this job

Medical, dental and vision coverage

Life insurance

401K with company contribution

Wellness program

Job summary

Fresenius Kabi in Grand Island, NE is seeking a supervisor to oversee liquid production personnel and processes on the assigned shift, coordinating scheduling, preparation, filling, and capping activities.

You will drive continuous improvements, ensure cGMP compliance, train staff, review batch records, and partner with management to meet production goals. The role requires strong communication and a background in a FDA-regulated environment.

Qualifications

• BS/BA degree preferred; work experience in lieu of a degree possible.
• Supervisory experience in a production/manufacturing environment.
• Proven oral and written communication and proofreading skills.
• Detail oriented with proficiency in MS Office (Excel/Word/Access) preferred.
• Experience in an FDA-regulated industry preferred (3-5 years).

Responsibilities

• Coordinate daily/weekly production schedule for the area.
• Oversee assigned shift production processes on the floor.
• Collaborate with management and other functions to coordinate support activities.
• Drive continuous process improvements and root cause analysis.
• Ensure safety, cGMP compliance, and policy adherence.
• Coordinate staffing and training for the area.
• Develop and deliver staff training; evaluate performance.
• Communicate across operations to share information.
• Support product release through batch record review.
• Develop SOPs and contribute to documentation.
• Provide production data for monthly reports and efficiency metrics.

Skills

Supervisory experience

Communication skills

Detail-oriented

Office software proficiency

Education

BS/BA in life sciences or engineering

Tools

Microsoft Office Suite

Job description

Fresenius Kabi in Grand Island, NE is seeking a supervisor to oversee liquid production personnel and processes on the assigned shift, coordinating scheduling, preparation, filling, and capping activities.

You will drive continuous improvements, ensure cGMP compliance, train staff, review batch records, and partner with management to meet production goals. The role requires strong communication and a background in a FDA-regulated environment.