Supervisor, Production (3rd Shift)

Fresenius Group; Grand Island, Northern (NE, KY); Hybrid; USD 74,000 - 103,000; Full time

Benefits offered by this job

Medical, dental and vision coverage

Life insurance

Disability insurance

401K with company contribution

Wellness program

Job summary

Fresenius Kabi in Grand Island, Nebraska, seeks a supervisor for liquid production to coordinate scheduling and oversee on‑the‑floor activities.

You will work the 10 PM–6:30 AM shift, ensuring cgMP compliance, staff training, and continuous process improvements. Final pay reflects experience and qualifications in a regulated manufacturing environment.

Qualifications

• BS/BA in life sciences or engineering preferred; work experience considered.
• Previous supervisory experience in production/manufacturing.
• Strong oral and written communication and proofreading skills.
• Detail oriented with proficiency in Microsoft Office.

Responsibilities

• Coordinate daily/weekly production schedule per area managers.
• Oversee assigned shift production processes on the floor.
• Interact with management and other functions to coordinate support.
• Empower personnel to define and implement process improvements.
• Complete deviation investigations with root-cause analysis.
• Ensure compliance with policies, safety programs, and cgMPs.
• Coordinate staffing and ensure staff training is up to date.
• Develop and execute staff training programs and evaluate performance.
• Establish communication methods for continuity across shifts.
• Support product release by reviewing production batch records.
• Create and review departmental Standard Operating Procedures.
• Provide production data for monthly reports and line efficiency.

Skills

Supervisory experience

Communication skills

Attention to detail

Microsoft Office

Education

BS/BA in life sciences or engineering

Tools

Excel

Word

Access

Job description

Job Summary

Responsible for the supervision and coordination of liquid production personnel and processes within an assigned area of responsibility. Control may include but is not limited to; scheduling and organizing component preparation, Terminally Sterilized filling, and capping.

Salary Range: $73,614 - $103,000 Annually + 6% Bonus
Hours: M-F; 10PM-6:30AM

Final pay determinations will depend on various factors, including, but not limited to experience level, education, knowledge, skills, and abilities.

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.
• Interacts with department management and other functional areas to coordinate all support activities relating to their assigned area.
• Empowers assigned personnel to engage in defining and recommending continuous process improvements,
• 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.
• Develops and executes training and follow-up programs to enhance staff development. Regularly evaluates performance of operations personnel.
• Establishes effective communication methods to provide continuity of information across all operations and shifts.
• Supports product release through the efficient review and completion of production batch records.
• Creates, revises and reviews departmental Standard Operating Procedures.
• Provides production data to managers in support of monthly reports and line efficiency tracking.
• Assumes other duties as assigned by production management.
• Works overtime as required.

Requirements

• BS/BA degree in life sciences or engineering discipline preferred (work experience in lieu of a degree is possible)
• Previous supervisory experience in a production/manufacturing environment.
• Proven oral and written communication and proofreading skills required.
• Detail oriented and proficient computer skills: d Microsoft Office software, including Excel, Word, and Access preferred.
• Previous experience in an FDA regulated industry preferred (3-5 years).

Additional Information

We offer an excellent salary and benefits package including medical, dental andvision coverage, as well as life insurance, disability, 401K with company contribution,and wellness program.

Please note that joining our team does not create a guaranteed or permanentemployment arrangement. All employment is at‑will, meaning both the employeeand Fresenius Kabi have the right to end the employment relationship at any time,in accordance with applicable federal and state laws.

Fresenius Kabi is an Equal Opportunity/Affirmative Action employer. All qualified applicantswill receive consideration for employment without regard to race, color, religion, sex, national origin,citizenship, immigration status, disabilities, or protected veteran status.