Regulatory Affairs Specialist

Job SummaryThis role involves managing product registrations, submitting regulatory documents, preparing regulatory files, and updating technical files to comply with the Medical Device Regulation (MDR).Key ResponsibilitiesReview and update technical files to ensure compliance with the Medical Device Regulation (MDR).Develop and implement regulatory...

Job SummaryThis role involves managing product registrations, submitting regulatory documents, preparing regulatory files, and updating technical files to comply with the Medical Device Regulation (MDR).Key ResponsibilitiesReview and update technical files to ensure compliance with the Medical Device Regulation (MDR).Develop and implement regulatory...

Regulatory Affairs at Hobson Prior**Job Summary**We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Hobson Prior. As a key member of our regulatory team, you will be responsible for managing product registrations, submitting regulatory documents, and preparing regulatory files to ensure compliance with the Medical Device...

Regulatory Affairs at Hobson Prior**Job Summary**We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Hobson Prior. As a key member of our regulatory team, you will be responsible for managing product registrations, submitting regulatory documents, and preparing regulatory files to ensure compliance with the Medical Device...

Hobson Prior is seeking a highly skilled Regulatory Affairs Specialist to manage product registrations, submit regulatory documents, and maintain technical files in compliance with the Medical Device Regulation (MDR). The ideal candidate will have a strong understanding of regulatory standards and the ability to handle complex regulatory situations.Key...

Hobson Prior is seeking a highly skilled Regulatory Affairs Specialist to manage product registrations, submit regulatory documents, and maintain technical files in compliance with the Medical Device Regulation (MDR). The ideal candidate will have a strong understanding of regulatory standards and the ability to handle complex regulatory situations.Key...

{"h1":"Regulatory Affairs Specialist","p":"Wir suchen einen erfahrenen Regulatory Affairs Specialist, der sich auf die internationale Registrierung und Anmeldung von chemischen Stoffen spezialisiert hat. Als Teil unseres Teams werden Sie sich um die Sicherstellung der sicheren Verwendung von registrierten chemischen Stoffen kümmern und die Einhaltung der...

{"h1":"Regulatory Affairs Specialist","p":"Wir suchen einen erfahrenen Regulatory Affairs Specialist, der sich auf die internationale Registrierung und Anmeldung von chemischen Stoffen spezialisiert hat. Als Teil unseres Teams werden Sie sich um die Sicherstellung der sicheren Verwendung von registrierten chemischen Stoffen kümmern und die Einhaltung der...

Job SummaryThis role involves managing product registrations, submitting regulatory documents, and preparing regulatory files to ensure compliance with the Medical Device Regulation (MDR).Key ResponsibilitiesReview and update technical files to ensure compliance with the Medical Device Regulation (MDR).Manage product registrations and submit regulatory...

Job SummaryThis role involves managing product registrations, submitting regulatory documents, and preparing regulatory files to ensure compliance with the Medical Device Regulation (MDR).Key ResponsibilitiesReview and update technical files to ensure compliance with the Medical Device Regulation (MDR).Manage product registrations and submit regulatory...

Job SummaryHobson Prior is seeking a highly skilled Senior Manager/Director of Regulatory Affairs to join our team. As a key member of our organization, you will be responsible for managing product registrations, submitting regulatory documents, preparing regulatory files, and updating technical files to comply with the Medical Device Regulation (MDR).Key...

Job SummaryHobson Prior is seeking a highly skilled Senior Manager/Director of Regulatory Affairs to join our team. As a key member of our organization, you will be responsible for managing product registrations, submitting regulatory documents, preparing regulatory files, and updating technical files to comply with the Medical Device Regulation (MDR).Key...

Beschreibung der PositionWir suchen einen engagierten Kollegen als Qualitäts- und Regulatory Affairs Manager zur Verstärkung unseres Qualitätsmanagement- und Regulatory Affairs-Teams in Tübingen.HauptraumfelderAufrechterhaltung und Weiterentwicklung des Regulatory Affairs-ProzessesDurchführung von Konformitätsbewertungsverfahren für...

Beschreibung der PositionWir suchen einen engagierten Kollegen als Fachmann für Qualitätsmanagement und Regulatory Affairs zur Verstärkung unseres Qualitätsmanagement- und Regulatory Affairs-Teams in Tübingen.HauptraumfelderAufrechterhaltung, Pflege und Weiterentwicklung des Regulatory Affairs-Prozesses in Zusammenarbeit mit den...

Corporate Vice President Quality Assurance & Regulatory AffairsAbout Our Company :ACE Partners is a leading global Medical Device company specialising in Class III Cardiovascular Devices. Our innovations significantly impact patient outcomes, and we are at the forefront of the industry in both Europe and the U.S.Position Overview :We are seeking a dynamic...

Corporate Vice President Quality Assurance & Regulatory AffairsAbout Our Company :ACE Partners is a leading global Medical Device company specialising in Class III Cardiovascular Devices. Our innovations significantly impact patient outcomes, and we are at the forefront of the industry in both Europe and the U.S.Position Overview :We are seeking a dynamic...

Corporate Vice President Quality Assurance & Regulatory AffairsAbout Us :We're a leading global Medical Device company specialising in Class III Cardiovascular Devices. Our innovations significantly impact patient outcomes, and we are at the forefront of the industry in both Europe and the U.S.Position Overview :We are seeking a dynamic Senior Director of...

Corporate Vice President Quality Assurance & Regulatory AffairsAbout Us :We're a leading global Medical Device company specialising in Class III Cardiovascular Devices. Our innovations significantly impact patient outcomes, and we are at the forefront of the industry in both Europe and the U.S.Position Overview :We are seeking a dynamic Senior Director of...

JobbeschreibungWir suchen einen engagierten Kollegen (m/w/d) als Qualitätsmanager (m/w/d) für unser Qualitätsmanagement & Regulatory Affairs-Team in Tübingen.HauptraumfelderRegulatory Affairs-Prozess: Aufrechterhaltung, Pflege und Weiterentwicklung des Regulatory Affairs-Prozesses in Zusammenarbeit mit den...

Unser Kunde ist ein renommierter und moderner Anbieter von chemischen Produkten.AufgabenInternationale Registrierung und Anmeldung von chemischen Stoffen im Rahmen von EU-REACH, Japan, Korea, Türkei und UKSicherstellung der sicheren Verwendung von registrierten chemischen StoffenBewertung von Produkten, die in Europa in Verkehr gebracht werden, hinsichtlich...