Die KI-Suchmaschine für Jobs
Regulatory Affairs Manager - Labeling & Regulatory Intelligence(m/w/x)
Beschreibung
In this role, you will play a crucial part in shaping regulatory strategies and ensuring compliance for medicinal products. Daily tasks will involve reviewing data sheets, coordinating translations, and optimizing labeling processes while collaborating with local regulatory teams.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •Completed scientific studies in natural sciences or pharmacy
- •Pharmacist license
- •2+ years of professional experience in pharmaceutical industry
- •Experience in regulatory affairs
- •Experience with labeling
- •Strong knowledge of international regulatory frameworks and standards
- •Strong project management and analytical thinking ability
- •Team player with excellent communication and problem-solving abilities
- •Business fluent in German and English
Ausbildung
Berufserfahrung
2 Jahre
Aufgaben
- •Review Company Core Data Sheets (CCDS)
- •Implement CCDS into national product information texts for EEA, CH, and UK
- •Coordinate translations and ensure compliance and timely provision
- •Initiate, review, and approve artwork changes for EEA, CH, and UK
- •Collaborate closely with local regulatory affairs
- •Support submissions and responses to authority queries
- •Optimize labeling and artwork processes
- •Train colleagues on the artwork management system
- •Act as a key user for Merz’ artwork management system
- •Lead and monitor the Regulatory Intelligence process in Global Regulatory Affairs
- •Further develop the Regulatory Intelligence process
Sprachen
Deutsch – verhandlungssicher
Englisch – verhandlungssicher
Benefits
Attraktive Vergütung
- •Attractive remuneration
Sonstige Vorteile
- •Extensive social benefits
- •Attractive location
Karriere- und Weiterentwicklung
- •Individual career development
Flexibles Arbeiten
- •Hybrid work model
Familienfreundlichkeit
- •Good work-life balance
Parkplatz & Pendelvorteile
- •Good transport links
Modernes Büro
- •Modern workplaces
Gratis oder Vergünstigte Mahlzeiten
- •Company restaurant
Lockere Unternehmenskultur
- •Flat hierarchies
- •Open corporate culture
Sonstige Zulagen
- •Employer-subsidized benefits
Gesundheits- & Fitnessangebote
- •WellPass
Öffi Tickets
- •Deutschland-ticket
Mitarbeiterrabatte
- •Corporate Benefits
Firmenfahrrad
- •JobBike
- Merz TherapeuticsVollzeitmit HomeofficeSeniorFrankfurt am Main
- Merz Therapeutics
Team Lead Regulatory Affairs Regions(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main - Merz Therapeutics
Regulatory CMC Writing Manager(m/w/x)
Vollzeitmit HomeofficeManagementFrankfurt am Main - STADA Arzneimittel AG
Senior Director Regulatory Global Specialty / Biosimilar Development(m/w/x)
Vollzeitmit HomeofficeSeniorBad Vilbel - Sanofi-Aventis Deutschland GmbH
Regulatory Site Officer(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenFrankfurt am Main
Regulatory Affairs Manager - Labeling & Regulatory Intelligence(m/w/x)
Die KI-Suchmaschine für Jobs
Beschreibung
In this role, you will play a crucial part in shaping regulatory strategies and ensuring compliance for medicinal products. Daily tasks will involve reviewing data sheets, coordinating translations, and optimizing labeling processes while collaborating with local regulatory teams.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •Completed scientific studies in natural sciences or pharmacy
- •Pharmacist license
- •2+ years of professional experience in pharmaceutical industry
- •Experience in regulatory affairs
- •Experience with labeling
- •Strong knowledge of international regulatory frameworks and standards
- •Strong project management and analytical thinking ability
- •Team player with excellent communication and problem-solving abilities
- •Business fluent in German and English
Ausbildung
Berufserfahrung
2 Jahre
Aufgaben
- •Review Company Core Data Sheets (CCDS)
- •Implement CCDS into national product information texts for EEA, CH, and UK
- •Coordinate translations and ensure compliance and timely provision
- •Initiate, review, and approve artwork changes for EEA, CH, and UK
- •Collaborate closely with local regulatory affairs
- •Support submissions and responses to authority queries
- •Optimize labeling and artwork processes
- •Train colleagues on the artwork management system
- •Act as a key user for Merz’ artwork management system
- •Lead and monitor the Regulatory Intelligence process in Global Regulatory Affairs
- •Further develop the Regulatory Intelligence process
Sprachen
Deutsch – verhandlungssicher
Englisch – verhandlungssicher
Benefits
Attraktive Vergütung
- •Attractive remuneration
Sonstige Vorteile
- •Extensive social benefits
- •Attractive location
Karriere- und Weiterentwicklung
- •Individual career development
Flexibles Arbeiten
- •Hybrid work model
Familienfreundlichkeit
- •Good work-life balance
Parkplatz & Pendelvorteile
- •Good transport links
Modernes Büro
- •Modern workplaces
Gratis oder Vergünstigte Mahlzeiten
- •Company restaurant
Lockere Unternehmenskultur
- •Flat hierarchies
- •Open corporate culture
Sonstige Zulagen
- •Employer-subsidized benefits
Gesundheits- & Fitnessangebote
- •WellPass
Öffi Tickets
- •Deutschland-ticket
Mitarbeiterrabatte
- •Corporate Benefits
Firmenfahrrad
- •JobBike
Über das Unternehmen
Merz Therapeutics
Branche
Pharmaceuticals
Beschreibung
Das Unternehmen ist ein führendes Pharma-Unternehmen, das Menschen mit Bewegungsstörungen und anderen gesundheitlichen Beschwerden hilft.
- Merz Therapeutics
Global Regulatory Lead - New Assets(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main - Merz Therapeutics
Team Lead Regulatory Affairs Regions(m/w/x)
Vollzeitmit HomeofficeSeniorFrankfurt am Main - Merz Therapeutics
Regulatory CMC Writing Manager(m/w/x)
Vollzeitmit HomeofficeManagementFrankfurt am Main - STADA Arzneimittel AG
Senior Director Regulatory Global Specialty / Biosimilar Development(m/w/x)
Vollzeitmit HomeofficeSeniorBad Vilbel - Sanofi-Aventis Deutschland GmbH
Regulatory Site Officer(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenFrankfurt am Main