Aktuelle Jobs im Zusammenhang mit Regulatory Affairs Specialist - Frankfurt am Main, Hessen - elemed
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Regulatory Affairs Specialist
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Regulatory Affairs Specialist
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Regulatory Affairs Specialist Medical Devices EU
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Regulatory Affairs Specialist
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Regulatory Affairs Specialist
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Regulatory Affairs Specialist
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Frankfurt am Main, Hessen, Deutschland LORENZ Life Sciences Group VollzeitÜbernahme von HerausforderungenWir suchen nach einem motivierten und erfahrenen Regulatory Affairs-Experten, der sich für die Steigerung der Effizienz des Arzneimittelzulassungsprozesses begeistert. Als Teil unseres Teams wirst du die bestehenden Prozesse unserer Kunden analysieren und dokumentieren, um ihre Konfigurationsanforderungen zu definieren.Deine...
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Regulatory Affairs Specialist
vor 4 Wochen
Frankfurt am Main, Hessen, Deutschland LORENZ Life Sciences Group VollzeitÜbernahme von HerausforderungenWir suchen nach einem motivierten und erfahrenen Regulatory Affairs-Experten, der sich für die Steigerung der Effizienz des Arzneimittelzulassungsprozesses begeistert. Als Teil unseres Teams wirst du die bestehenden Prozesse unserer Kunden analysieren und dokumentieren, um ihre Konfigurationsanforderungen zu definieren.Deine...
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Regulatory Affairs Specialist
vor 2 Wochen
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Regulatory Affairs Specialist
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Regulatory Affairs Specialist
vor 3 Wochen
Frankfurt am Main, Hessen, Deutschland Grifols VollzeitJob Title: Regulatory Affairs ManagerWe are seeking a highly skilled Regulatory Affairs Manager to join our team at Grifols. As a key member of our regulatory affairs team, you will be responsible for ensuring compliance with European regulatory requirements and laws.Key Responsibilities:Coordinate European Marketing Authorization maintenance and regulatory...
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Regulatory Affairs Specialist
vor 3 Wochen
Frankfurt am Main, Hessen, Deutschland Grifols VollzeitJob Title: Regulatory Affairs ManagerWe are seeking a highly skilled Regulatory Affairs Manager to join our team at Grifols. As a key member of our regulatory affairs team, you will be responsible for ensuring compliance with European regulatory requirements and laws.Key Responsibilities:Coordinate European Marketing Authorization maintenance and regulatory...
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Regulatory Affairs Specialist
vor 3 Wochen
Frankfurt am Main, Hessen, Deutschland Deutsche Börse AG VollzeitJob Title: Regulatory Affairs SpecialistDeutsche Börse Group is seeking a highly skilled Regulatory Affairs Specialist to join our Group Regulatory Strategy team. As a key member of our team, you will be responsible for monitoring and analyzing political and regulatory initiatives, positioning Deutsche Börse Group towards political and regulatory...
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Regulatory Affairs Specialist
vor 3 Wochen
Frankfurt am Main, Hessen, Deutschland Deutsche Börse AG VollzeitJob Title: Regulatory Affairs SpecialistDeutsche Börse Group is seeking a highly skilled Regulatory Affairs Specialist to join our Group Regulatory Strategy team. As a key member of our team, you will be responsible for monitoring and analyzing political and regulatory initiatives, positioning Deutsche Börse Group towards political and regulatory...
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Regulatory Affairs Specialist
vor 1 Monat
Frankfurt am Main, Hessen, Deutschland VWR International GmbH, part of Avantor VollzeitRegulatory Affairs Officer GermanyWe are seeking a highly skilled Regulatory Affairs Officer to join our team at VWR International GmbH, part of Avantor. As a key member of our regulatory team, you will be responsible for ensuring compliance with German and EU regulations.Key Responsibilities:Monitor and track new and updated legislation affecting our...
Regulatory Affairs Specialist
vor 2 Monaten
Job Title: Regulatory Affairs Specialist
Job Summary:
We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Elemed. As a key member of our quality management team, you will be responsible for maintaining and improving our Quality Management System (QMS), leading audits, and driving regulatory compliance at product development stages.
Key Responsibilities:
- Maintain and improve the Quality Management System (QMS) according to ISO 13485
- Collaborate with and guide cross-functional internal and external supplier teams to create new CAPA and document control processes
- Work with clients on product performance data to create post-market related reports
- Hands-on experience in maintaining QMS at an IVD manufacturer
- Strong written and verbal communication skills in English
About Elemed:
We serve within the Medical device, diagnostic and combination device arena, working with Managers up to VP of Quality and Regulatory. Our team helps medical device experts of today become leaders of tomorrow.
Our Mission:
At Elemed, we recruit exceptional people that solve regulatory and compliance problems, so patients can have access to safe, innovative and life-changing Medical Devices.
