Production Supervisor

For over three decades, Cirtec Medical has been a leading outsourcing partner for complex medical devices. We specialize in providing comprehensive solutions for Class II and III devices, from design and development to precision components and finished device assembly. Our expertise spans neuromodulation, implantable drug delivery, cardiac rhythm management, structural heart, mechanical circulatory support, and minimally invasive surgical systems. Our dedicated teams prioritize growth, innovation, and collaboration.

About the role

Lead the Production Team in the manufacturing of rubber molded medical devices and pharmaceutical components in their assigned area on the designated shift. Products may include: closures for pharmaceutical packaging, stoppers, seals, and O-rings. Works closely with manufacturing engineering, quality, and human resources. Primary deliverables are in safety, quality, cost, and inventory performance while adhering to production and project schedules and budgets.

Responsibilities

• Develop and manage manufacturing processes to meet or exceed product standards under safe conditions and in accordance with production schedules and good manufacturing practices, ensuring the most effective and efficient use of available resources.
• Review product documentation and manufacturing operational documentation to ensure compliance and accuracy. Utilize appropriate systems, procedures, and cross-functional input to manage revisions to documents, processes, and products.
• Deploy lean and six-sigma processes to identify opportunities to improve service, minimize scrap, reduce manufacturing costs, and enhance product quality.
• Enforce all safety and Standard Operating Procedures, ensuring compliance with all corporate and regulatory requirements including ISO, FDA-QSR, and other global standards.
• Motivate and develop production associates to meet current and future business challenges.
• Establish a safe and secure facility environment, utilizing associate participation to improve housekeeping, cleanliness, and quality.
• Ensure compliance with all OSHA training requirements and regulations.
• Evaluate employees through performance reviews, ongoing coaching, and feedback methods.
• Monitor facility metrics (Work Management System) to ensure optimum performance from associates at all levels.
• Lead or participate in safety-related initiatives, including accident investigations.
• Plan and coordinate equipment repairs with Planning, Engineering, and the Maintenance team in case of malfunctions.
• Troubleshoot process-related issues and take corrective actions for nonconformances to product or equipment, in conjunction with Shift Process Technicians.
• Maintain associates' time and schedules within the payroll system.
• Assist in operator training.
• Perform other duties as assigned.

Requirements

• High school diploma or general education degree (GED) required.
• Three to five years of experience supervising associates in a manufacturing environment.
• Ability to read, comprehend, and write detailed instructions, correspondence, and memos.
• Proficiency in basic arithmetic: addition, subtraction, multiplication, and division using whole numbers, common fractions, and decimals. Ability to comprehend rates, percentages, and interpret bar graphs.

Qualifications

• Associate Degree or higher in management, business, or an engineering discipline preferred.
• Practical experience and certification in Lean/Six Sigma manufacturing preferred.
• Prior supervisory or management experience in a union environment is preferred.
• Self-starter with a demonstrated ability to motivate others.
• High-volume medical device manufacturing experience, particularly working with the FDA, is a plus.

Pay

$80,000 - $85,000