Director, Manufacturing

Overview Argon Medical Devices is a global manufacturer of specialty medical products, headquartered in Plano, Texas. Argon offers a broad line of medical devices for Interventional Radiology, Vascular Surgery, Interventional Cardiology and Oncology. Argon’s brand is recognized for best-in-class products that improve patient outcomes via percutaneous, image-guided procedures. Our values describe what we believe in and how we operate. These values are our moral compass which guide our decisions and define the deeply held beliefs and principles of our organizational culture. Argon Medical is a family of individuals united by a mission and culture which continue to grow stronger every day. ARGON MEDICAL DEVICES IS NOT LEVERAGING SEARCH FIRMS Position Overview The Director of Manufacturing is responsible for overseeing and coordinating the daily operations of production, maintenance, and machine shop departments to meet manufacturing goals. This role focuses on improving systems, processes, and resource utilization to drive productivity, quality, and efficiency. The Director will serve as a key member of the facility leadership team and collaborate across departments to ensure successful manufacturing outcomes. Responsibilities Lead and direct manufacturing activities to meet objectives related to safety, quality, service, cost and inventory. Collaborate with purchasing, planning, engineering and quality teams to ensure seamless operations and effective resource utilization. Drive process improvements to reduce costs and improve efficiency and labor productivity. Ensure cGMP-compliant production and maintain a strong focus on quality and regulatory compliance. Participate in facility-level meetings and share best practices on Lean Manufacturing, Six Sigma, and other operational excellence methodologies. Provide monthly input into labor, spending, and absorption forecasts. Supervise and support production teams through frontline leadership and technical guidance. Partner with Quality and Engineering to ensure adherence to specifications, drawings, and production documentation. Evaluate and implement improved manufacturing methods, layouts, and workflows. Analyze staffing needs, space utilization, and equipment layout to optimize manufacturing flow. Provide key inputs to management related to production timelines, labor needs, and cost projections. Collaborate across departments to align manufacturing with company objectives. Mentor and develop supervisory personnel through training, feedback, and career development support. Perform other duties as assigned. Supervisory Responsibilities Coaching and developing employees. Planning, scheduling, and reviewing work. Conducting performance evaluations. Participating in hiring and onboarding. Managing disciplinary actions, including terminations. Overseeing salary and compensation decisions within scope. Skills for Success Bachelor’s degree from a four-year accredited institution required. Minimum of 8–10 years of experience in medical device or regulated manufacturing environments required. Proven experience leading manufacturing teams and implementing improvement methodologies (Lean, Kanban, 5S, Visual Manufacturing) required. Preferred Education and Experience Experience in FDA-regulated environments or ISO-certified operations is highly preferred. Travel Less than 15% travel required. #J-18808-Ljbffr