Dual-Shift Manufacturing Supervisor II: Lead & Improve

Baxter International Inc.

Marion (NC)

On-site

USD 81,000 - 99,000

Full time

10 days ago

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Benefits offered by this job

Shift flexibility
Medical, Dental and Vision coverage
Paid Time Off
401K match
Employee Stock Purchase Program
Paid Parental Leave
Tuition Reimbursement

Job summary

Baxter is seeking a Manufacturing Supervisor II in Marion, NC to lead two shifts, drive safety, quality, and regulatory compliance, and develop a high-performing team. You will guide continuous improvement, manage performance, and partner with Quality, Engineering, and Supply Chain to meet production goals.

Qualified candidates have 4+ years of leadership in a regulated manufacturing setting, strong communication, and experience with cGMP.

Qualifications

  • Bachelor's degree in Engineering, Life Sciences, Manufacturing, or related field with 3+ years manufacturing experience.
  • 4+ years leading or managing employees in manufacturing/regulatory setting.
  • Working knowledge of cGMP, quality systems, regulatory requirements.
  • Strong leadership, prioritization, and achieving operational goals.
  • Experience with metrics analysis and root cause identification.
  • Excellent communication with frontline staff and cross-functional partners.

Responsibilities

  • Lead daily manufacturing operations on both day and night shift to achieve production schedules, quality targets, and customer commitments while maintaining compliance with regulatory standards.
  • Coach, develop, and support team members through performance management, training, career development, and ongoing feedback to build a high-performing workforce.
  • Drive continuous improvement initiatives that enhance productivity, product quality, operational efficiency, and resource utilization.
  • Monitor manufacturing metrics and operational performance, identify opportunities for improvement, and implement corrective actions to achieve business objectives.
  • Review and approve manufacturing documentation, batch records, and operational reports to support timely product release and regulatory compliance.
  • Partner with cross-functional teams including Quality, Engineering, Supply Chain, and Operations to resolve manufacturing issues, implement process improvements, and support new product or equipment introductions.
  • Lead investigations, troubleshooting efforts, audits, and regulatory inspection activities while promoting a culture of safety, quality, and accountability.

Skills

Leadership
cGMP knowledge
Audits
Process improvement
Communication
Manufacturing systems

Education

Bachelor's degree in Engineering
Life Sciences background
Associate degree with experience

Tools

ERP systems

Job description

Baxter is seeking a Manufacturing Supervisor II in Marion, NC to lead two shifts, drive safety, quality, and regulatory compliance, and develop a high-performing team. You will guide continuous improvement, manage performance, and partner with Quality, Engineering, and Supply Chain to meet production goals.

Qualified candidates have 4+ years of leadership in a regulated manufacturing setting, strong communication, and experience with cGMP.

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