Argon Medical Devices, Inc.
Production Supervisor: Guide Wires
Argon Medical Devices, Inc.
Argon Medical Devices, Inc.
1445 Flat Creek Rd.
75751 Athens , TX
Responsibilities Include: 

Assure maximum utilization of resources to meet the scheduled due dates for product availability.  Balance throughput by scheduling resources and equipment to ensure attainment of established production goals and objectives.

  • Identify opportunities for improved equipment utilization
  • Recognize equipment malfunctions and process drifts.
  • Responsible for continual improvement of safety, quality and production processes while ensuring compliance with ISO/GMP/FDA and quality standards.
  • Provide adequate training and close coaching for the department employees to establish product awareness and understanding, cGMP compliance and promote ISO 13485 quality standards.
  • Implement safety programs to include training and awareness to eliminate lost time accidents and reduce OSHA recordable injuries.
  • Serve as a communication link between management and the department to assure quality information flow.
  • Provide effective leadership and coaching to members of department, including goal setting, performance feedback and salary administration.
  • Alert management to any capacity constraints that have a potential to adversely affect the customer service levels.
  • Maintain the floor stock inventory to assure adequate components availability.
  • Assist in the development of annual operation budgets, provide updates and manage variances.
  • Obtain Engineering, Materials management and Q.A. support as necessary to achieve the department’s thru-put and budget objectives.
  • Maintain an environment of fairness, challenge and support to foster job effectiveness and a sense of direction and well-being in the department employees. Respond to all employee concerns in an efficient manner.
  • Maintain the department integrity in terms of cGMP compliance.
  • Follow all safety policies procedures.
  • Other responsibilities as assigned.
  • AA/AS with 4 years or BA/BS or equivalent on the job training
  • 2 years direct line supervisory experience in an industrial environment with knowledge of medical components, ISO/cGMP and FDA regulations, or equivalent on the job training