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Production Supervisor

Job in Kalamazoo, Kalamazoo County, Michigan, 49006, USA
Listing for: DSJ Global
Full Time position
Listed on 2026-08-15
Job specializations:
  • Manufacturing / Production
    Production Manager, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 80000 - 90000 USD Yearly USD 80000.00 90000.00 YEAR
Job Description & How to Apply Below

Production Supervisor (PR/605597) Kalamazoo, Michigan

Salary: USD
80000 - USD
90000 per annum

A growing pharmaceutical manufacturer is seeking experienced Production Supervisors for both 2nd Shift and 3rd Shift operations. These positions offer the opportunity to join a highly regulated manufacturing environment where safety, quality, compliance, and operational excellence are top priorities.

They are looking for hands-on leaders who can effectively manage production teams, drive performance, and ensure products are manufactured in compliance with cGMP standards and FDA regulations. Successful candidates will have a proven track record of leading teams, improving efficiencies, and fostering a strong culture of accountability and continuous improvement.

Key Responsibilities:

  • Provide day-to-day leadership, coaching, and development for production associates while promoting a culture centered on safety, quality, and compliance.
  • Ensure manufacturing operations are executed according to cGMP requirements, SOPs, batch records, and regulatory standards.
  • Drive attainment of production schedules while maximizing productivity, minimizing downtime, and maintaining product quality.
  • Monitor and analyze key performance indicators including throughput, labor efficiency, scrap, downtime, and overall equipment effectiveness (OEE).
  • Partner closely with Quality, Maintenance, Engineering, Supply Chain, and Warehouse teams to resolve operational challenges and support business objectives.
  • Lead shift meetings, performance discussions, investigations, corrective actions, and employee development activities.
  • Support deviation investigations, CAPAs, change controls, and audit readiness initiatives.
  • Maintain accurate production documentation and ensure compliance with all company and regulatory requirements.

Qualifications:

  • 2+ years of supervisory experience within manufacturing environments.
  • Strong understanding of cGMP regulations, FDA requirements, quality systems, and manufacturing best practices.
  • Demonstrated ability to lead teams, develop talent, and drive a culture of accountability.
  • Experience managing production performance metrics and implementing process improvements.
  • Strong communication, problem-solving, and decision-making skills.
  • Bachelor's degree required

Why Consider This Opportunity?

  • Opportunity to join a stable, expanding pharmaceutical organization with significant growth potential.
  • Competitive compensation, bonus potential, and comprehensive benefits package.
  • Highly visible leadership role with direct impact on manufacturing performance, employee development, and site success.
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