Night Production Supervisor — GMP & Process Improvement

Fresenius Kabi

Melrose Park (IL)

On-site

USD 80,000 - 100,000

Full time

14 days+

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Benefits offered by this job

401(k) with company contributions
Medical, dental, and vision coverage
Paid vacation and holidays
Life insurance
Disability benefits
Wellness program

Job summary

Fresenius Kabi in Melrose Park, IL is seeking a production supervisor to oversee liquid production processes, scheduling, and cGMP compliance on their shift.

The role focuses on coordinating daily manufacturing activities, training staff, investigating deviations, and driving continuous improvements across the line. Strong leadership and experience in FDA-regulated environments are essential. This is a full-time position with competitive benefits.

Qualifications

  • Bachelor’s degree or relevant work experience in production/manufacturing.
  • Minimum five years in production/manufacturing; at least two in leadership.
  • Experience in FDA-regulated environment strongly preferred.

Responsibilities

  • Coordinate daily/weekly production schedule based on area production managers.
  • Oversee assignment on shift and coordinate production activities on the floor.
  • Coordinate staffing and ensure personnel training is up to date.
  • Develop and execute training and follow-up programs for staff development.
  • Investigate deviations, perform root cause analysis, and implement corrective actions.
  • Ensure compliance with policies, safety programs, standards and cGMPs.

Skills

Leadership
Process improvement
Cross-functional collaboration
Documentation & SOPs
Staff training

Education

Bachelor's degree or equivalent

Job description

Fresenius Kabi in Melrose Park, IL is seeking a production supervisor to oversee liquid production processes, scheduling, and cGMP compliance on their shift.

The role focuses on coordinating daily manufacturing activities, training staff, investigating deviations, and driving continuous improvements across the line. Strong leadership and experience in FDA-regulated environments are essential. This is a full-time position with competitive benefits.

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