Descripción y detalle de las actividades 1. Defines sites strategy to reach long and medium-term objectives. 2. Create monthly reports for the department management to guarantee Key Performance Indicator compliance. 3. Lead SIOP (Sales, Inventory, and Operations Planning) 4.
_The Quality Engineer will be responsible for providing Quality Management System compliance support for Centerpiece. The scope of this role encompasses activities related to Documentation Control, Change Control, Corrective Action Systems, EQMS Implementation & Administration, Field
The Production Supervisor oversees daily manufacturing operations within the cleanroom / controlled environment, ensuring that CENTERPIECE’s medical devices are produced safely, efficiently, and in compliance with regulatory standards such as FDA, ISO 13485, and GMP. This