quality procedures and standards in order to achieveand maintain adequate results; - Actively participate in audit activities.
Work Experience - Required Qualifications
• At least 3 years' experience with Regulatory Affairs in the medical device industry...
Randstad Italia SpA-Sestri Levante, 9 km da Carasco
in ingresso e uscita
• audit interno di processi e prodotto
• controllo dei materiali in accettazione
• controllo delle specifiche a disegno
• collaborazione con Team Leader per analisi e risoluzione problemi
• verifica di quanto previsto nelle istruzioni...
quality procedures and standards in order to achieveand maintain adequate results; - Actively participate in audit activities.
Work Experience - Required Qualifications
• At least 3 years' experience with Regulatory Affairs in the medical device industry...
Randstad Italia Spa-Sestri Levante, 9 km da Carasco
pranzo. Si offre: inserimento diretto in azienda dopo periodo di prova. Inquadramento: Impiegato livello D – RAL: 27.000 € Responsabilit Di cosa si occuper l'addetto controllo qualit che stiamo cercando? validazione dei prodotti in ingresso e uscita audit...
quality procedures and standards in order to achieveand maintain adequate results; - Actively participate in audit activities.
Work Experience - Required Qualifications
• At least 3 years' experience with Regulatory Affairs in the medical device industry...
quality procedures and standards in order to achieveand maintain adequate results; - Actively participate in audit activities.
Work Experience - Required Qualifications
• At least 3 years' experience with Regulatory Affairs in the medical device industry...
achieveand maintain adequate results;Actively participate in audit activities.Work Experience
• Required Qualifications• At least 3 years' experience with Regulatory Affairs in the medical device industry preferred;
• ISO 13485• Fluent in English;
• Internal...
quality procedures and standards in order to achieveand maintain adequate results; - Actively participate in audit activities.
Work Experience - Required Qualifications
• At least 3 years' experience with Regulatory Affairs in the medical device industry...