Participate in New Product Development Risk Analysis, including FMEA and PFMEA.Assist in supplier qualification, develop receiving inspection, and Ship to Stock (SOS) program.Work with different departments to develop and review processes ensuring product quality, such as inspection techniques, raw material inspections, and in-process checks.Investigate customer concerns, perform evaluations, and prepare CAPAs for non-conforming products.Lead process validation for equipment and processes.Prepare documentation for UL, IEC, and FDA submissions as required by Regulatory Affairs.
Job Details
| ID | #53370534 |
| Estado | Wisconsin |
| Ciudad | Fonddulac |
| Tipo de trabajo | Full-time |
| Salario | USD TBD TBD |
| Fuente | Basic American Medical Products |
| Showed | 2025-01-30 |
| Fecha | 2025-01-30 |
| Fecha tope | 2025-03-31 |
| Categoría | Etcétera |
| Crear un currículum vítae | |
| Aplica ya | |