Production Supervisor - 2nd/3rd Shift

Position Overview IRP Medical is seeking a Production Supervisor that will cover the 2nd/3rd shift (Primary shifts: 2pm-10pm, hours are flexible). This position is responsible for the overall production and supervision of the assigned departments during the evening production shifts at the IRP Med facility. The role works closely with operations leadership and engineering to ensure alignment with IRP Med directives and initiatives. It is a hands‑on leadership position that actively contributes to business growth through the positive trending of customer related metrics. Key performance metrics for this role include Safety, Quality, Employee Supervision and Retention, Productivity, On‑Time Delivery, Cost‑out, and EBITDA. The supervisor will work in a dynamic, fast‑paced team environment, applying Lean manufacturing practices to deliver world‑class results in efficiency, quality, and productivity. IRP Medical manufactures high‑quality silicone and elastomer components for medical and life‑science applications, and is committed to precision, cleanliness, and supporting products that advance patient care. Employees join a team dedicated to excellence, problem solving, and meaningful impact in the healthcare industry. Essential Duties and Responsibilities Directs assigned shift operations in alignment with strategic and business plans and goals. Mitigates legal risks by documenting performance management, employee relations, investigations, safety, and worker compensation in compliance with employment laws. Manages, develops, and leads talent within the organization. Drives positive customer experience and actively contributes to continuous improvement. Utilizes Lean continuous improvement across all areas to improve cost, quality, and efficiency. Provides a safe work environment focused on 5S, risk reduction, and data‑driven decision making. Supports and executes level loading production schedules for capacity analysis and staffing. Schedules customer orders daily to meet on‑time delivery and quality requirements. Supports all capital projects related to the area of responsibility. Reviews routers to ensure accurate and appropriate steps in the manufacturing process. Ensures compliance with all local, state, and federal regulatory agencies, including OSHA and AQMD. Ensures compliance with all local, state, and federal licenses and permits in the assigned department. Ensures equipment is properly maintained and operates safely. Leads production and coordinates with inventory control functions to meet customer needs efficiently. Works with planning and sales to support customer requests and delivery commitments. Works extended days and/or weekends with flexibility to switch shifts as required. Embodies the company mission, vision, and values. Assumes other duties as assigned. Education and Experience Requirements Associate degree required (Engineering or Business Administration preferred). Minimum of 8+ years of experience in a manufacturing environment with at least 4 years in a similar supervisory role. Experience in Medical Device, Aerospace, or polymer manufacturing environments preferred. Experience in a low volume/high mix manufacturing environment. Experience in Lean Manufacturing. Experience in MRP/ERP systems. Ability to maintain a safe working environment through proper housekeeping, safety, and EHS procedures and practices, and OSHA compliance. Understanding of manufacturing technologies and processes. All applicants must be U.S. persons under ITAR. Competencies Excellent communication skills (verbal, written, listening); ability to adjust style for multiple audiences and facilitate group coaching. Strong people skills: maintain a positive attitude, motivate, coach, and provide feedback. Capability to face challenging situations and build trust‑based relationships. Ability to manage multiple priorities with strong organizational and planning skills. Strong mechanical aptitude and root‑cause problem‑solving skills. High energy level and excellent follow‑up. Proficient computer skills in Microsoft Office and working knowledge of MRP/ERP. Training Requirements On‑the‑job training on procedures and work instructions in the area of responsibility. Yearly refresher training on FOD, calibration, documentation control, and safety topics. Benefits IRP Medical offers a comprehensive benefits package, including medical, dental, vision, short- and long-term disability coverage, accident insurance, critical illness insurance, basic and supplemental life insurance, employee assistance plan, retirement savings and matching, and other developmental opportunities. Shift Details Primary shifts: 2pm–10pm (hours are flexible). 2nd shift: 2:00pm–10:30pm. 3rd shift: 10:00pm–6:30am. Equal Employment Opportunity IRP Medical is an Equal Opportunity Employer. We consider all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other legally protected status. Applicants requiring reasonable accommodation to complete the application process may contact Human Resources. ITAR Compliance This position requires access to information subject to the International Traffic in Arms Regulations (ITAR). Employment is contingent upon the applicant being a “U.S. person” as defined by ITAR (22 CFR § 120.15). Additional Information Actual placement within the salary range is dependent on multiple factors, including but not limited to skills, education, experience, and location. #J-18808-Ljbffr Kamatics Corporation