Develop, implement, and optimize automated manufacturing processes for Class II medical devices to ensure efficiency, quality, and compliance.
Lead the programming, integration, and troubleshooting of PLC systems for automated equipment used in the manufacturing process.
Document and maintain process validation, equipment qualification, and change control activities in accordance with quality management system standards.
Design and develop control systems for process automation and machine integration.
Experience:
3-5 years of experience in process engineering, with a strong focus on automated equipment and PLC systems in a regulated manufacturing environment.
Previous experience in the design, optimization, and maintenance of processes in the medical device industry, particularly with Class II medical devices, is preferred (ISO 13485)
Strong experience with PLC programming and troubleshooting (e.g., Allen Bradley, Siemens, or equivalent).
Experience with process validation and equipment qualification processes in a regulated environment.