Position Summary

The 2nd shift Production Supervisor is responsible for overseeing daily manufacturing operations on 2nd shift to ensure safe, efficient, and compliant production within a regulated medical device environment. This role leads a team of production employees, drives continuous improvement, and ensures adherence to quality systems, regulatory requirements, and company standards at IPG Medical. Production Operations Supervise and coordinate daily 2nd shift production activities to meet output, quality, and delivery targets

Monitor workflow, staffing levels, and production schedules to ensure optimal efficiency

Identify and resolve production issues in real time to minimize downtime

Ensure proper use of equipment, tools, and materials Team Leadership Lead, coach, and develop a team of production associates, technicians, and/or operators

Conduct performance management activities including feedback, coaching, and evaluations

Schedule staffing to meet production needs, including overtime planning as necessary

Promote a culture of accountability, teamwork, and continuous improvement Quality & Compliance Ensure strict adherence to FDA, ISO, GMP, and other regulatory requirements

Maintain compliance with IPG Medical quality systems and standard operating procedures (SOPs)

Support audits (internal and external) and corrective/preventive actions (CAPA)

Ensure documentation accuracy and completeness Safety Maintain a safe work environment by enforcing safety policies and procedures

Conduct safety audits, risk assessments, and incident investigations

Promote a strong safety culture and ensure compliance with OSHA standards Continuous Improvement Drive Lean manufacturing initiatives and process improvements

Participate in root cause analysis and problem-solving activities

Track and report key performance indicators (KPIs) such as yield, efficiency, scrap, and downtime

Collaborate cross-functionally with Engineering, Quality, and Supply Chain teams

Required Bachelor's degree in Manufacturing, Engineering, or related field OR equivalent experience

3-5+ years of experience in a manufacturing environment, preferably in medical devices or a regulated industry

1+ years of supervisory or team leadership experience

Strong knowledge of

GMP, FDA

regulations, and quality systems

Excellent problem-solving, organizational, and communication skills Preferred Experience with Lean Manufacturing, Six Sigma, or continuous improvement tools

Familiarity with ERP/MRP systems

Prior experience in medical device manufacturing Key Competencies Leadership & Team Development

Decision Making & Problem Solving

Attention to Detail & Quality Focus

Communication & Collaboration

Results Orientation

Adaptability in a fast-paced environment Work Environment Manufacturing floor environment with exposure to equipment and controlled production areas

Must be able to stand for extended periods of time

May require flexible hours, including evenings or weekends, depending on production needs