Remote Regulatory Submissions Specialist — EU IVDR/CE
Salva questo lavoro e mantieni la tua ricerca organizzata
Crea un account gratuito per salvare lavori, creare avvisi e tornare a questa inserzione dalla tua dashboard.
Continuando accetti i nostri Termini & Informativa sulla privacy.
Mira, a fast-growing femtech company, seeks a Regulatory Submission Specialist to lead and support regulatory documentation for in vitro diagnostic devices. You will ensure compliance across technical documentation and regulatory programs while collaborating with internal teams and external consultants.
The role emphasizes EU IVDR CE-marking readiness, post-market surveillance, and cross-functional coordination in a remote, fast-paced startup environment that serves a global market.
-
lombardia, lombardia, Italia Mira Tempo pienoMira, a fast-growing femtech company, seeks a Regulatory Submission Specialist to lead and support regulatory documentation for in vitro diagnostic devices. You will ensure compliance across technical documentation and regulatory programs while collaborating with internal teams and external consultants. The role emphasizes EU IVDR CE-marking readiness,...
-
Regulatory Submission Specialist
2 giorni fa
Lombardia, Lombardia, Italia Mira Da remoto Tempo pieno 81.000 € - 116.000 € ContrattoAbout MiraMira is a San Francisco-based hormonal health company providing integrative care and hormonal testing for over 300,000 customers. In 2023, we were recognized by Inc. 5000 as America's fastest-growing femtech company.About MiraMira is a San Francisco-based hormonal health company providing integrative care and hormonal testing for over 300,000...
-
lombardia, lombardia, Italia Mira Tempo pienoMira, a San Francisco-based hormonal health company, seeks a Regulatory Submission Specialist to lead regulatory documentation for IVD devices. You will ensure evidence supports claims, align labeling, and coordinate with internal teams and external consultants to maintain compliance throughout the product lifecycle. The role requires EU IVDR experience,...
-
Romano di Lombardia, Lombardy, Italia Mira Tempo pieno 81.000 € - 116.000 € ContrattoMira, a fast-growing femtech company, seeks a Regulatory Submission Specialist to lead and support regulatory documentation for in vitro diagnostic devices.Le informazioni riportate di seguito illustrano i requisiti del ruolo, l'esperienza richiesta ai candidati e le qualifiche associate.You will ensure compliance across technical documentation and...
-
Regulatory Submission Specialist
18 ore fa
Romano di Lombardia, Lombardy, Italia Mira Tempo pienoMira is a San Francisco-based hormonal health company providing integrative care and hormonal testing for over 300,000 customers. In 2023, we were recognized by Inc. 5000 as America's fastest-growing femtech company.La preghiamo di leggere attentamente le informazioni contenute in questo annuncio di lavoro per comprendere esattamente cosa ci si aspetta dai...
-
Regulatory Submission Specialist
2 giorni fa
lombardia, lombardia, Italia Mira Tempo pienoMira is a San Francisco-based hormonal health company providing integrative care and hormonal testing for over 300,000 customers. In 2023, we were recognized by Inc. 5000 as America's fastest-growing femtech company. Mira’s breakthrough innovation was creating the market’s only FDA-compliant at-home hormone monitor with quantitative testing technology....
-
Romano di Lombardia, Lombardy, Italia Mira Tempo pienoMira, a San Francisco-based hormonal health company, seeks a Regulatory Submission Specialist to lead regulatory documentation for IVD devices.La descrizione completa del lavoro illustra tutte le competenze, l'esperienza pregressa e le qualifiche che i candidati dovrebbero possedere.You will ensure evidence supports claims, align labeling, and coordinate...
-
Lombardia, Lombardia, Italia Mira Tempo pienoMira, a San Francisco-based hormonal health company, seeks a Regulatory Submission Specialist to lead regulatory documentation for IVD devices. You will ensure evidence supports claims, align labeling, and coordinate with internal teams and external consultants to maintain compliance throughout the product lifecycle. The role requires EU IVDR experience,...