Production Supervisor, GMP & Biotech Manufacturing

Fresenius Kabi USA, LLC; Melrose Park (IL); On-site; USD 80,000 - 100,000; Full time

Benefits offered by this job

401(k) plan with company contributions

paid vacation

holiday and personal days

employee assistance program

health benefits to include medical, 
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Job summary

Fresenius Kabi USA, LLC is seeking a Production Supervisor in Melrose Park, IL. The role oversees liquid production processes, coordinates daily/weekly schedules, and ensures completion of batch records in a cGMP environment.

Salary ranges from $80,000 to $100,000 with a 6% target bonus and comprehensive benefits. Responsibilities include coordinating staffing, enforcing SOPs, driving process improvements, and maintaining compliance with safety and regulatory programs.

Qualifications

• Bachelor's degree and/or relevant work experience required
• Minimum of five years experience in a production/manufacturing environment; with at least two years in a leadership role
• Experience in a FDA-regulated industry strongly preferred

Responsibilities

• Coordinates the execution of the daily/weekly production schedule based upon direction from the area production managers.
• Oversees the production processes on their assigned shift, working on the production floor to coordinate all relevant production activities.
• Completes thorough deviation investigations in a timely fashion, performing detailed root cause analysis and implementing corrective and preventative actions.
• Assures the compliant application of departmental and company policies and procedures, safety programs, standards and cGMP's.
• Coordinates staffing for their assigned area of responsibility and assures personnel training is up to date.

Skills

Production supervision

Lean manufacturing

SOP adherence

Root cause analysis

Education

Bachelor's degree

Job description

Fresenius Kabi USA, LLC is seeking a Production Supervisor in Melrose Park, IL. The role oversees liquid production processes, coordinates daily/weekly schedules, and ensures completion of batch records in a cGMP environment.

Salary ranges from $80,000 to $100,000 with a 6% target bonus and comprehensive benefits. Responsibilities include coordinating staffing, enforcing SOPs, driving process improvements, and maintaining compliance with safety and regulatory programs.