Mehrer Jahre Berufserfahrung in einem relevanten Regulatory Affairs Bereich (EU, CH), bevorzugt mit pflanzlichen Arzneimitteln. Kenntnisse von Regulatory Information Management Software (RIMS) und in elektronischen Datenbanken wie SPOR, Eudravigilance/Art 57 sind von Vorteil. ...
Reporting to the Head of Regulatory Affairs, the Quality & Regulatory Affairs Specialist is responsible for delivering end to end regulatory package under ODM-Distributor scheme in compliance with established quality management system, overseeing (but not limited to) initial compilation of desig...
Mehrer Jahre Berufserfahrung in einem relevanten Regulatory Affairs Bereich (EU, CH), bevorzugt mit pflanzlichen Arzneimitteln. Kenntnisse von Regulatory Information Management Software (RIMS) und in elektronischen Datenbanken wie SPOR, Eudravigilance/Art 57 sind von Vorteil. ...
Reporting to the Head of Regulatory Affairs, the Quality & Regulatory Affairs Specialist is responsible for delivering end to end regulatory package under ODM-Distributor scheme in compliance with established quality management system, overseeing (but not limited to) initial compilation of design co...
La nuova risorsa verrà inserita all’interno dell’area di registrazione .Il profilo ricercato si occuperà di:.Allestimento della documentazione necessaria per i nuovi processi registrativi nei paesi extra-Europei: .Preparazione delle variazioni volte al mantenimento del life cycle delle registrazioni...
Kenntnisse von Regulatory Information Management Software (RIMS) und in elektronischen Datenbanken wie SPOR, Eudravigilance/Art 57 sind von Vorteil Sehr gute mündliche und schriftliche Englisch- und Deutschkenntnisse Gute Kenntnisse im resp. ...
Regulatory Affairs Specialist II Johnson & Johnson - Switzerland & United States Are you ready to take your career in Regulatory Affairs to the next level and make a significant impact? Join our dynamic team at Johnson & Johnson, where your expertise will play a crucial role in ensuring our inn...
As a key EUDAMED Data Specialist, you will work closely with the project lead to support a data collection and validation project to implement the regulatory requirements of the EU Medical Devices Regulation regarding the European Database for Medical Devices (EUDAMED). Interest in regulatory topics...
Regulatory Affairs Specialist (m/w/d). Erste Berufserfahrung im Bereich Regulatory Affairs, vorzugsweise in der pharmazeutischen Industrie. ...
REGULATORY AFFAIRS SPECIALIST. Esperienzaminima di 2/3 anni maturata nel ruolo di Regulatory Affairs Specialist inambito farmaceutico;. Buonaconoscenza dei principali strumenti informatici e dei programmi di RegulatoryAffairs (es. ...
Process and maintain EMEA, renewals, changes, Free Sale Certificates, and other regulatory certificates. Update of the technical documentation taking into account regulatory requirements. Maintain regulatory affairs files and listing and distribute information as required. Proofread, assemble, route...
The Regulatory Affairs Specialist is responsible for leading substantial and complex regulatory projects. As a member of the Regulatory organization, this position works with management to establish the overall strategic direction for Regulatory Affairs and works collaboratively across multiple inte...
As the Regulatory Affairs Specialist, you will play a critical role in enabling the PHC business for the relevant portfolio within and outside Europe. You will coordinate Regulatory Life Cycle Management activities across multiple countries, ensuring compliance with regulatory requirements and maint...
Regulatory Banking Specialist . We help create sustainable change by stimulating innovation, unlocking data possibilities, navigating risk and regulatory complexity, optimising deals, and aligning costs with business strategy to create a competitive advantage. Bereich Regulatory Affairs bei einer Ba...
Mehrer Jahre Berufserfahrung in einem relevanten Regulatory Affairs Bereich (EU, CH), bevorzugt mit pflanzlichen Arzneimitteln. Kenntnisse von Regulatory Information Management Software (RIMS) und in elektronischen Datenbanken wie SPOR, Eudravigilance/Art 57 sind von Vorteil. ...
As an integral member of our Quality Unit, you will be accountable for change control assessment, compliance of manufacturing activities vs regulatory filing, provision of regulatory documents and regulatory intelligence and local expertise in RA. ...
Your Mission: You will be responsible for the development and upkeep of regulatory documentation to ensure compliance with global standards. Develop and execute regulatory strategies aligned with business objectives. Create, submit, and maintain regulatory documentation, including technical files an...
Become part of a group that enables its customers to meet some of the greatest challenges in patient treatment and join us by applying for Quality Assurance Expert for pharmaceutical QMS and combination products. Assist the line functions in the creation and monitoring of quality processes related t...
Produkt Manager, Product Manager, Produkt Spezialist, Product Specialist. Sales, Sales Representative, Account Manager. ...
Hast du Lust, dich in einem innovativen Fintech einzubringen? Wir bieten dir die einmalige Gelegenheit, unsere Erfolgsgeschichte weiterzuschreiben.Du bist verantwortungsvoll, am Puls der Zeit und magst Tätigkeiten mit einem hohen Wirkungsgrad und kurzen Entscheidungswegen? Dann herzlich willkommen b...
Erfahrung im Vertrieb und Marketing, vorzugsweise im Bereich Brand oder Product Management, Business Development, idealerweise im Bereich Food & Beverage. ...
Verpackungen sind unsere Leidenschaft! .Die Firma Wipf AG entwickelt und produziert hochdichte Verpackungsfolien und Beutel für die Lebensmittel-, Pharma- und Non-Food-Industrie.Das Unternehmen beschäftigt ca.Proaktives Monitoring und Implementierung von Gesetzesänderungen .Regulatorische Prüfung un...
Herr Pascal Forster, Recruiting Specialist, Telefon +41 33 227 74 02. ...
Du beurteilst Product Quality Reviews (PQR). ...
Weitere GMP Tätigkeiten, wie Freigabe, CTD/DMF und anderen Filing Dokumenten, Quality Agreements, Product Quality Reviews. ...