e a riporto del Quality Manager, si occuperà di:
• Gestione degli aspetti regolatori e certificatori di prodotto con capacità di valutazione degli aspetti regolatori specifici applicabili
• Elaborazione ed aggiornamento delle schede tecniche...
lead our Technical Department for Medical Devices Regulation (EU) 2017/745 (MDR). This is a strategic leadership role with full responsibility for driving the accreditation process as a Notified Body and, once accredited, managing certification...
It's more than a job
In an administrative role at Kuehne+Nagel, tasks such as managing office operations or coordinating schedules certainly contribute to your team's success, but they also provide meaningful moments for people around the world...
Position: Quality Manager – Medical Devices / Conformity Assessment Body
Location: Primarily remote (with regular coordination meetings on-site and/or online)
Type: Full-time
About Certexe
Certexe is a newly founded Italian company...
It's more than a job
In an administrative role at Kuehne+Nagel, tasks such as managing office operations or coordinating schedules certainly contribute to your team's success, but they also provide meaningful moments for people around the world...
sita in zona Mantova. La persona si occuper di monitorare il sistema qualit in riferimento alla normativa ISO 13485, seguendo prevalentemente la parte legata a medical device e parafarmaco. Tra le attivit effettuer : • supporto al Quality Manager...
It's more than a job
In an administrative role at Kuehne+Nagel, tasks such as managing office operations or coordinating schedules certainly contribute to your team's success, but they also provide meaningful moments for people around the world...
a eventi e congressi locali e nazionali;
• Collaborare e mantenere una comunicazione efficace con le figure aziendali interne rilevanti (Medical Affairs, Responsabili Commerciali, Marketing e Business Operations Manager), secondo necessità;
• Garantire...
procedures and IRB/EC policies and procedures). The Senior CRA conducts monitoring visits as identified by the monitoring plan, study team or department needs to evaluate data accuracy and subject safety required by review of regulatory documents, medical...