Production Team Lead - Daily Ops & Coaching

Baxter International Inc.

Kentucky

On-site

USD 54,000 - 75,000

Full time

2 days ago
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Benefits offered by this job

Health insurance
401(k) Retirement Savings Plan (RSP)
Paid holidays
Paid time off
Employee Stock Purchase Plan (ESPP)
Commuting benefits
Educational assistance programs

Job summary

Baxter International Inc. is seeking an Assistant Supervisor to lead daily production operations, oversee scheduling and staffing, and ensure compliance with FDA standards.

You will coordinate with department leadership, drive continuous improvement, and maintain line communications while supporting training and documentation efforts. The role requires 1-2 years in manufacturing and a high school diploma, with preference for knowledge of medical device regulations.

Qualifications

  • High School diploma or equivalent is required.
  • 1-2 years manufacturing experience preferred.
  • Working knowledge of medical device regulations is preferred.

Responsibilities

  • Lead the day-to-day production, scheduling, staffing, and auditing activities to meet customer requirements and company standards.
  • Resolve production issues, monitor line status, and escalate problems as needed.
  • Ensure materials and documentation are available to the line at all times.
  • Maintain line communications and status updates; provide guidance and leadership.
  • Identify training needs with department leadership and assist with improvements.
  • Write NCRs and support continuous improvement initiatives.

Education

High School diploma or equivalent

Job description

Baxter International Inc. is seeking an Assistant Supervisor to lead daily production operations, oversee scheduling and staffing, and ensure compliance with FDA standards.

You will coordinate with department leadership, drive continuous improvement, and maintain line communications while supporting training and documentation efforts. The role requires 1-2 years in manufacturing and a high school diploma, with preference for knowledge of medical device regulations.

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