1. Experience in connectors or connector cord sets is preferred, and experience in overseas production factories is preferred. 2. Responsible for production process scheduling and directing the product manufacturing process 3. Responsible for the management of production, shipment, material inventory and other factory affairs 4. Manage the production schedule, delivery date and output in the factory to increase production capacity/reduce costs efficiently 5. Execute production and meet quality requirements 6. Coordinate internal production and sales to jointly improve customer satisfaction 7. Do not exclude career development in other subsidiaries.
1. Plan, implement and coordinate activities related to quality system, quality assurance, quality verification, customer problem handling and daily management of the department. 2. Collection and update of domestic/foreign medical device regulatory certifications and related regulations and standards. 3. ISO13485 and GMP quality system audit related matters. 4. Matters related to domestic/foreign medical device clinical trials.