Production Supervisor, Manufacturing Operations

1 day ago


Sturgis, Michigan, United States Abbott Laboratories company Full time
About the Role

This is a challenging and rewarding opportunity to join the Abbott Laboratories company as a Production Supervisor, Manufacturing Operations. As a key member of our team, you will be responsible for leading a single shift of a multi-shift manufacturing operations line, with additional accountability for providing overall manufacturing leadership for afternoon or night shift manufacturing operations.

Key Responsibilities
  • Model and promote the behaviors that ensure delivery of high-quality products for our customers while championing compliance with Abbott policies and procedures, meeting all local and statutory requirements and adhering to the regulatory requirements of countries to which products are shipped.
  • Initiate, manage, and make decisions which impact product quality.
  • Model and promote a thorough understanding of what drives product costs, profitability and cash flow within the shift, team, and department, while operating within budget with a focus on margin, material utilization and Cost Improvement Program (CIP) goals.
  • Train others in this understanding for operator engagement and involvement in cost management.
  • Share accountability for line budgetary decisions with direct manager.
  • Track, trend and continuously improve budgetary performance for overtime (OT), direct expenses, operating equipment effectiveness (OEE), labor, downtime, schedule performance (units per hour, Lbs./Hour), year over year CIP and material usage.
Requirements
  • Bachelor's degree in business, science, food technology or engineering OR equivalent combination of education and work experience.
  • 2+ years' experience working in manufacturing.
  • Proven leadership capabilities.
  • Project planning & execution experiences.
  • Process control knowledge.
  • Proven plant financial understanding.
  • Experience with working on Continuous Improvement Projects.
Preferred Qualifications
  • Previous experience working in a regulated manufacturing work environment.
  • Experience utilizing project planning and execution tools.
  • Knowledge of FDA 21 CFR and other regulatory requirements for Infant Formula.


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