Descripción y detalle de las actividades- Purpose of the position: The ME will be responsible for supporting production activities in the medical device industry including yield improvement initiatives, product disposition, continuous improvement activities, assembly procedure development, and process validations.Additional responsibilities will include the transfer of new products and processes into manufacturing, process optimization, mistake proofing, process risk analysis, design reviews and provide input on design for manufacturing.Key Tasks & Responsibilities: - Create, write, and execute process validations.
- Participate and execute validation strategy.
- Lead Projects with some supervision.
- Support and lead continuous improvement activities and yield improvement initiatives.
- Develop, update pFMEA.
- Support production on non-conformances, determine root cause and develop solutions.
- Write engineering technical reports.
- Experience with equi...