Global Regulatory Submissions Specialist

Enovis sta cercando uno Regulatory Market Access Specialist per supportare l'ingresso di dispositivi medici nel mercato e garantire la conformità continua. Ruolo chiave nel preparare submission regolatorie e nelle attività di mantenimento della registrazione prodotti a livello internazionale. Richiesta una laurea in disciplina scientifica/tecnica, almeno 2...

Azienda Anonima è alla ricerca di uno Global Regulatory Affairs Specialist da inserire in un team internazionale nel settore Life Sciences. Il ruolo comprende gestione regolatoria end-to-end, collaborazione con funzioni trasversali e contatti con mercati internazionali. Il candidato ideale ha una laurea in discipline scientifiche, esperienza in Regulatory...

Overview Within the Global Regulatory Affairs Operations department, whose mission is to provide timely and high-quality regulatory submission-ready packages to facilitate faster time to market, while driving business solutions that support the company’s cross-functional processes and advancing company’s digital capabilities, the resource, reporting to...

Chi siamo ENOVIS™ Enovis Corporation (NYSE: ENOV) è un'azienda in crescita nel settore delle tecnologie mediche orientata all'innovazione e dedicata allo sviluppo di soluzioni clinicamente differenziate che migliorano in modo misurabile i risultati dei pazienti e trasformano i flussi di lavoro. Grazie a una cultura del miglioramento continuo, al talento...

Job Description We are seeking a Regulatory Business Partner to support the growth and delivery of consulting services within our Regulatory Consulting business unit for Life Sciences clients. This role acts as a bridge between regulatory strategy and execution, combining business development, project leadership, and deep regulatory expertise to deliver...

Overview Quality Assurance Regulatory Affairs (QARA) Specialist – Dedalus. Remote in Italy. Part of the Global Quality and Assurance Team to drive quality and regulatory excellence in healthcare technology. What you’ll achieve As a QARA Specialist you will ensure compliance with Quality and Regulatory standards across the company, contributing to better...

Select how often (in days) to receive an alert: Alfasigma is a privately held global healthcare company founded over 75 years ago in Italy, where it remains headquartered today in Bologna and Milan. The Group operates in over 100 markets spanning Europe, North and South America, Asia, and Africa. Over three years ago, we embarked on a transformative journey...

Allucent is seeking an experienced Regulatory Affairs Coordinator to support site start-up activities for clinical trials. You will manage regulatory documents, track milestones in CTMS/eTMF, and prepare local submissions to regulators in coordination with the Global Regulatory team. A Life Science degree and 2+ years in regulatory affairs are required, with...

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,...