Production Supervisor (2nd Shift)

About the Role

Join Safecor Health—a growing industry leader dedicated to improving patient safety and supporting healthcare systems nationwide. We are transforming the way medications reach patients through innovative pharmaceutical unit-dose packaging solutions. As a Production Supervisor, you will lead a team in a highly regulated, quality-driven environment, driving operational success and making a direct impact on patient safety and employee development.

This is a hands-on leadership role where you will oversee daily production operations, develop high-performing teams, and ensure operational excellence. You will work on the production floor, coaching employees, solving problems in real time, and contributing to continuous improvement initiatives.

Core Values

• Care: We care deeply about our employees, customers, and the patients we ultimately serve.
• Commitment: We do what's right, follow through on our promises, and hold ourselves accountable.
• Excellence: We continuously strive to improve, innovate, and deliver exceptional results.

Why Join Safecor Health?

• Join a rapidly growing healthcare manufacturing company with a meaningful mission.
• Lead a talented team in a highly regulated, quality-driven environment.
• Make a direct impact on operational performance, employee development, and patient safety.
• Be part of continuous improvement initiatives that shape the future of our organization.
• Work alongside collaborative leaders who value innovation, accountability, and teamwork.
• Enjoy opportunities for professional growth and career advancement as we continue to expand.

Responsibilities

• Lead, coach, and develop Production Technicians and team members to achieve safety, quality, and productivity goals.
• Oversee daily production operations, ensuring compliance with cGMP, SOPs, regulatory requirements, and company policies.
• Maintain a safe, organized, and efficient production environment while promoting a culture of accountability and continuous improvement.
• Manage staffing, scheduling, work assignments, training, and employee performance to support operational objectives.
• Monitor attendance, timekeeping, and employee relations activities, including performance management and corrective action when necessary.
• Review production documentation and batch records to ensure accuracy, completeness, and audit readiness.
• Maintain an active floor presence to troubleshoot issues, minimize downtime, and drive operational efficiencies.
• Partner with cross-functional teams to support site initiatives, process improvements, and business growth objectives.
• Ensure accurate ERP transactions and documentation while supporting employee training on system processes.
• Monitor departmental performance metrics, budgets, and resources to achieve operational goals.
• Serve as a resource for production processes, equipment, serialization, and aggregation activities.
• Communicate effectively across shifts and departments to ensure alignment, collaboration, and successful execution of priorities.

Requirements

• Bachelor's degree or equivalent experience required.
• 2+ years of experience in pharmaceutical manufacturing, cGMP, ISO, or a regulated production environment.
• Prior supervisory or team leadership experience preferred.

Skills & Abilities

• Strong leadership, coaching, and team development skills.
• Knowledge of manufacturing processes and quality systems in a regulated environment.
• Excellent problem-solving, organizational, and communication skills.
• Proficiency with Microsoft Office and business systems.
• Strong attention to detail and commitment to quality, safety, and compliance.

Physical & Work Environment

• Ability to lift up to 50 pounds and perform frequent standing, walking, bending, and other physical activities.
• Comfortable working in a production, warehouse, and office environment.
• Ability to wear required PPE and work safely around manufacturing equipment.