Aktuelle Jobs im Zusammenhang mit (Senior) Team Lead Regulatory Affairs - Tübingen - NES Global Deutschland GmbH NES Fircroft


  • Tübingen, Baden-Württemberg, Deutschland Hobson Prior Vollzeit

    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...


  • Tübingen, Baden-Württemberg, Deutschland Hobson Prior Vollzeit

    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...


  • Tübingen, Baden-Württemberg, Deutschland ACE Partners Vollzeit

    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...


  • Tübingen, Baden-Württemberg, Deutschland ACE Partners Vollzeit

    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...


  • Tübingen, Baden-Württemberg, Deutschland ACE Partners Vollzeit

    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...


  • Tübingen, Baden-Württemberg, Deutschland ACE Partners Vollzeit

    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...


  • Tübingen, Baden-Württemberg, Deutschland ACE Partners Vollzeit

    Transformative Leadership OpportunityAbout ACE Partners :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 Vice President of Regulatory Affairs...


  • Tübingen, Baden-Württemberg, Deutschland ACE Partners Vollzeit

    Transformative Leadership OpportunityAbout ACE Partners :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 Vice President of Regulatory Affairs...


  • Tübingen, Deutschland ACE Partners Vollzeit

    Corporate Vice President Quality Assurance & Regulatory AffairsAbout Us:We're working with 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 Vice...


  • Tübingen, Baden-Württemberg, Deutschland Hobson Prior Vollzeit

    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...


  • Tübingen, Baden-Württemberg, Deutschland Hobson Prior Vollzeit

    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...


  • Tübingen, Baden-Württemberg, Deutschland ACE Partners Vollzeit

    ACE Partners is seeking a seasoned leader to drive global regulatory and quality operations. As Vice President of Regulatory Affairs and Quality Assurance, you will be responsible for implementing and aligning global regulatory and quality strategies with corporate goals. This role requires a strong understanding of global regulatory requirements, including...


  • Tübingen, Baden-Württemberg, Deutschland ACE Partners Vollzeit

    ACE Partners is seeking a seasoned leader to drive global regulatory and quality operations. As Vice President of Regulatory Affairs and Quality Assurance, you will be responsible for implementing and aligning global regulatory and quality strategies with corporate goals. This role requires a strong understanding of global regulatory requirements, including...


  • Tübingen, Baden-Württemberg, Deutschland ACE Partners Vollzeit

    ACE Partners is seeking a seasoned leader to drive global regulatory and quality operations. As Vice President of Regulatory Affairs and Quality Assurance, you will be responsible for implementing and aligning global regulatory and quality strategies with corporate goals. This role requires a strong understanding of global regulatory requirements, including...


  • Tübingen, Baden-Württemberg, Deutschland ACE Partners Vollzeit

    ACE Partners is seeking a seasoned leader to drive global regulatory and quality operations. As Vice President of Regulatory Affairs and Quality Assurance, you will be responsible for implementing and aligning global regulatory and quality strategies with corporate goals. This role requires a strong understanding of global regulatory requirements, including...


  • Tübingen, Baden-Württemberg, Deutschland Hobson Prior Vollzeit

    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...


  • Tübingen, Baden-Württemberg, Deutschland Hobson Prior Vollzeit

    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...


  • Tübingen, Baden-Württemberg, Deutschland Hobson Prior Vollzeit

    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...


  • Tübingen, Baden-Württemberg, Deutschland Hobson Prior Vollzeit

    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...


  • Tübingen, Baden-Württemberg, Deutschland ACE Partners Vollzeit

    ACE Partners is seeking a seasoned leader to drive global regulatory and quality operations. As Vice President of Regulatory Affairs and Quality Assurance, you will be responsible for implementing and aligning global regulatory and quality strategies with corporate goals. This role requires a strong understanding of global regulatory requirements, including...

(Senior) Team Lead Regulatory Affairs

vor 4 Monaten


Tübingen, Deutschland NES Global Deutschland GmbH NES Fircroft Vollzeit

Unser Mandant ist ein traditionsreiches, deutsches Unternehmen und hat sich hinzu einem weltweit agierenden Konzern entwickelt. Mit dem Fokus auf Spezialchemikalien, die als Funktionsgeber, Hilfsmittel und Additive für industrielle Prozesse eingesetzt werden, tragen heute über 2.000 Mitarbeitende zum Erfolg des Unternehmens bei.

Tasks
  • Fachliche und disziplinarische Leitung eines RA-Teams
  • Registrierung und Anmeldung chemischer Stoffe gemäß globaler Chemikalienvorschriften (EU-REACH und Nicht-EU-Regionen)
  • Sicherstellung der sicheren Verwendung registrierter chemischer Stoffe durch die Bereitstellung von Sicherheitsberichten (CSRs)
  • Bewertung der Produkte für den europäischen Markt in Bezug auf die Einhaltung relevanter Vorschriften
  • Interne Kommunikation zu REACH-relevanten Themen sowie externe Kommunikation mit Lieferanten, Kunden und Behörden
  • Mitarbeit in Arbeitsgruppen von Industrieverbänden
  • Pflege und Weiterentwicklung von Datenbanken sowie Implementierung von Prozessen
Requirements
  • Abgeschlossenes naturwissenschaftliches Studium, gerne Chemie, Biologie, Toxikologie, Ökotoxikologie o.Ä.
  • Umfassende, praxisorientierte Kenntnisse im Chemikalienrecht und in der Registrierung (z.B. REACH, TSCA, K-REACH, KKDIK o.Ä.)
  • Erste Führungserfahrungen von Vorteil
  • Hervorragende Teamfähigkeit und Kommunikationsstärke
  • Selbständige und zielgerichtete Arbeitsweise sowie ausgeprägte analytische und konzeptionelle Fähigkeiten
  • Sehr gute schriftliche und mündliche Kommunikationsfähigkeiten in Englisch und idealerweise auch in Deutsch
Benefits
  • Urlaubsgeld 1.200 EUR
  • 13. Monatsgehalt
  • Tarifliche Altersvorsorge (Arbeitgeber finanziert)
  • Pflegezusatzversicherung
  • Zukunftsbetrag: bis zu zwei zusätzliche freie Tage
  • Erfolgsprämie
  • Möglichkeit für stillen Beteiligung (Unternehmenseinlage)
  • Jobrad & Gesundheitsmanagement
  • Kinderferienbetreuung (50% der Kosten werden übernommen)
  • 37,5h & Gleitzeit-Regelung
  • Bis zu 50% Homeoffice


NES Fircroft verfügt über mehr als 50 Jahre Erfahrung im Bereich des globalen Workforce-Management und der Rekrutierung von technischen Experten.