Post Market Surveillance Specialist
1 giorno fa
Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients— that is what Vantive aspires to deliver. We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous and don’t settle for the mediocre. Each of us is driven to help improve patients’ lives worldwide. Join us in advancing our mission to extend lives and expand possibilities. **Summary** The Post Market Management Technician is involved in activities related to Quality management. You will be part of an international team collaborating closely with Italian colleagues in Medolla site. **Essential duties and responsibilities** - Post-market surveillance activities; - Compliance management; - Interaction with health authorities and notified bodies; - Management of relations with other departments such as manufacturing, quality investigation, technical assistance, R&D; - PMS data collection and support PMS data analysis; - Participation and support during audits. **Qualifications** - Degree in scientific fields (CTF, Biology, Bioengineering...); - Previous experience in Post Market, Regulatory Affairs, Quality Assurance in Pharma/Medical industry is preferred; - Interpersonal and relational skills; - Team-working oriented; - Problem-solving attitude and smart approach; - Organizational and time management skills (flexibility); - Very Good knowledge of English (spoken and written) **Reasonable Accommodation** **Recruitment Fraud Notice** Vantive has discovered incidents of employment scams, where fraudulent parties pose as Vantive employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.
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Post Market Surveillance Specialist
1 settimana fa
Medolla, Italia Altro A tempo pienoVantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while...
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Post Market Surveillance Specialist
1 settimana fa
Medolla, Italia Vantive A tempo pienoVantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere.For 70 years, our team has driven meaningful innovations in kidney care.As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while...
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Post Market Surveillance Specialist
1 settimana fa
Medolla, Italia Altro A tempo pienoVantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while...
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Post Market Surveillance Specialist
1 settimana fa
Medolla, Italia Vantive A tempo pienoVantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while...
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Medolla, Italia Lavoropiu Spa A tempo pienoFarmapiù Bologna, divisione specialistica del gruppo Lavoropiù, cerca un/a Regulatory Affairs Specialist Senior con almeno 5/6 anni di esperienza nel ruolo e nel settore dispositivi medici per azienda cliente, produttore biomedicale, sita a Medolla (MO).La risorsa si occuperà di Gestire le attività di registrazione in ambito UE, FDA e altri paesi extra-...
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Medolla, Italia Lavoropiu Spa A tempo pienoFarmapiù Bologna, divisione specialistica del gruppo Lavoropiù, cerca un/a Regulatory Affairs Specialist Senior con almeno 5/6 anni di esperienza nel ruolo e nel settore dispositivi medici per azienda cliente, produttore biomedicale, sita a Medolla (MO). La risorsa si occuperà di Gestire le attività di registrazione in ambito UE, FDA e altri paesi extra-...
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medolla, Italia Lavoropiu Spa A tempo pienoFarmapiù Bologna, divisione specialistica del gruppo Lavoropiù, cerca un/a Regulatory Affairs Specialist Senior con almeno 5/6 anni di esperienza nel ruolo e nel settore dispositivi medici per azienda cliente, produttore biomedicale, sita a Medolla (MO).La risorsa si occuperà di Gestire le attività di registrazione in ambito UE, FDA e altri paesi extra-...
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Medolla, Italia Lavoropiu Spa A tempo pienoFarmapiù Bologna, divisione specialistica del gruppo Lavoropiù, cerca un/a Regulatory Affairs Specialist Senior con almeno 5/6 anni di esperienza nel ruolo e nel settore dispositivi medici per azienda cliente, produttore biomedicale, sita a Medolla (MO).La risorsa si occuperà di Gestire le attività di registrazione in ambito UE, FDA e altri paesi extra-...
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Medolla, Italia Lavoropiu Spa A tempo pienoFarmapiù Bologna, divisione specialistica del gruppo Lavoropiù, cerca un/a Regulatory Affairs Specialist Senior con almeno 5/6 anni di esperienza nel ruolo e nel settore dispositivi medici per azienda cliente, produttore biomedicale, sita a Medolla (MO).La risorsa si occuperà di Gestire le attività di registrazione in ambito UE, FDA e altri paesi extra-...
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MEDOLLA, Italia Lavoropiu Spa A tempo pienoFarmapiù Bologna, divisione specialistica del gruppo Lavoropiù, cerca un/a Regulatory Affairs Specialist Senior con almeno 5/6 anni di esperienza nel ruolo e nel settore dispositivi medici per azienda cliente, produttore biomedicale, sita a Medolla (MO). La risorsa si occuperà di Gestire le attività di registrazione in ambito UE, FDA e altri paesi...
