Responsibilities Responsible for the implementation and the optimization of robust manufacturing processes in Production ensuring that safety, effectiveness, quality and reliability of the devices are met. Lead PFMEA activities in coordination with other stakeholders. Generate and
Experteer Overview In this role you will optimize and validate manufacturing processes for FDA/ISO-regulated medical devices, ensuring safety, quality and reliability. You will lead risk and process-robustness activities, specify equipment and tooling, and collaborate across global
Gi Group, prima Agenzia per il Lavoro Italiana con oltre 200 filiali sul territorio nazionale e più di 1800 professionisti nel settore delle Risorse Umane RICERCA per Realtà di prodotto del settore Difesa, su Roma Laureandi