CHEPLAPHARM Arzneimittel GmbH
Senior Portfolio Owner Regulatory Affairs(m/w/x)
Vollzeitmit HomeofficeSenior
Greifswald, Berlin, Binningen
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CHCHEPLAPHARM Arzneimittel GmbH
Global Head of Regulatory Affairs(m/w/x)
Greifswald, Berlin, Binningen
Vollzeitmit HomeofficeSenior
Nejo KI-Zusammenfassung
Leading a global team of 80 regulatory professionals for a specialty pharma company. Driving regulatory strategies for product integration and lifecycle management. Master's degree and 10+ years of global regulatory expertise required. Work from another EU country up to 2 months/year, 30 days holiday.
Anforderungen
- Master’s degree in relevant scientific or pharmaceutical discipline
- More than 10 years professional experience in Regulatory Affairs
- Deep expertise in global regulatory requirements
- Deep expertise in submission processes across multiple markets
- Proven track record leading large regulatory organizations
- At least 10 years leadership experience
- Leadership experience in international and globally distributed teams
- Strong ability to build and maintain long-term relationships with regulatory authorities
- Strong ability to build and maintain long-term relationships with external partners
- Excellent communication skills
- Excellent leadership skills
- Indirect management across different hierarchical levels
Aufgaben
- Lead a global organization of 80 regulatory professionals
- Drive regulatory strategies for the product portfolio
- Focus on product integration and lifecycle management
- Ensure sustained market supply and portfolio continuity
- Support financial objectives through regulatory contributions
- Maintain global regulatory compliance and market authorizations
- Oversee regulatory assessments during due diligence
- Evaluate regulatory risks, timelines, and integration feasibility
- Make high-impact regulatory and strategic decisions
- Guide cross-functional teams for effective lifecycle management
- Foster alignment with enabling functions for regulatory operations
- Develop and lead a global regulatory team
- Promote collaboration, accountability, and operational excellence
- Ensure efficient use of enterprise systems and processes
Berufserfahrung
- 10 Jahre
Ausbildung
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
Benefits
Flexibles Arbeiten
- Individually customisable working models
- Working time account
Workation & Sabbatical
- Work from another EU country (up to 2 months/year)
Mehr Urlaubstage
- Compensatory time off
- 30 days of holiday
Sonstige Zulagen
- Flexible benefits budget
- Subsidies for meal costs
Betriebliche Altersvorsorge
- Company pension provision
Gesundheits- & Fitnessangebote
- Fitness and health offers
Öffi Tickets
- Subsidies for travel costs
Mitarbeiterrabatte
- Corporate benefits platform access
- Discounts at partner companies
Weiterbildungsangebote
- Internal training courses
- External training courses
Team Events & Ausflüge
- Company events
- Team events
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens CHEPLAPHARM Arzneimittel GmbH erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
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CHCHEPLAPHARM Arzneimittel GmbH
Global Head of Regulatory Affairs(m/w/x)
Greifswald, Berlin, Binningen
Vollzeitmit HomeofficeSenior
Nejo KI-Zusammenfassung
Leading a global team of 80 regulatory professionals for a specialty pharma company. Driving regulatory strategies for product integration and lifecycle management. Master's degree and 10+ years of global regulatory expertise required. Work from another EU country up to 2 months/year, 30 days holiday.
Anforderungen
- Master’s degree in relevant scientific or pharmaceutical discipline
- More than 10 years professional experience in Regulatory Affairs
- Deep expertise in global regulatory requirements
- Deep expertise in submission processes across multiple markets
- Proven track record leading large regulatory organizations
- At least 10 years leadership experience
- Leadership experience in international and globally distributed teams
- Strong ability to build and maintain long-term relationships with regulatory authorities
- Strong ability to build and maintain long-term relationships with external partners
- Excellent communication skills
- Excellent leadership skills
- Indirect management across different hierarchical levels
Aufgaben
- Lead a global organization of 80 regulatory professionals
- Drive regulatory strategies for the product portfolio
- Focus on product integration and lifecycle management
- Ensure sustained market supply and portfolio continuity
- Support financial objectives through regulatory contributions
- Maintain global regulatory compliance and market authorizations
- Oversee regulatory assessments during due diligence
- Evaluate regulatory risks, timelines, and integration feasibility
- Make high-impact regulatory and strategic decisions
- Guide cross-functional teams for effective lifecycle management
- Foster alignment with enabling functions for regulatory operations
- Develop and lead a global regulatory team
- Promote collaboration, accountability, and operational excellence
- Ensure efficient use of enterprise systems and processes
Berufserfahrung
- 10 Jahre
Ausbildung
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
Benefits
Flexibles Arbeiten
- Individually customisable working models
- Working time account
Workation & Sabbatical
- Work from another EU country (up to 2 months/year)
Mehr Urlaubstage
- Compensatory time off
- 30 days of holiday
Sonstige Zulagen
- Flexible benefits budget
- Subsidies for meal costs
Betriebliche Altersvorsorge
- Company pension provision
Gesundheits- & Fitnessangebote
- Fitness and health offers
Öffi Tickets
- Subsidies for travel costs
Mitarbeiterrabatte
- Corporate benefits platform access
- Discounts at partner companies
Weiterbildungsangebote
- Internal training courses
- External training courses
Team Events & Ausflüge
- Company events
- Team events
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens CHEPLAPHARM Arzneimittel GmbH erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
Gefällt dir diese Stelle?
BetaDein Career Agent findet täglich ähnliche Jobs für dich.
Über das Unternehmen
CHEPLAPHARM Arzneimittel GmbH
Branche
Pharmaceuticals
Beschreibung
Das Unternehmen ist ein globales und wachsendes Specialty Pharmaunternehmen mit einem außergewöhnlichen, nachhaltigen Geschäftsmodell.
Noch nicht perfekt?
- CHEPLAPHARM Arzneimittel GmbH
Senior Portfolio Owner Regulatory Affairs(m/w/x)
Vollzeitmit HomeofficeSeniorGreifswald, Berlin, Binningen - CHEPLAPHARM Arzneimittel GmbH
Global Head of Knowledge Hub(m/w/x)
Vollzeitmit HomeofficeSeniorGreifswald, Berlin, Binningen - CHEPLAPHARM Arzneimittel GmbH
Global Head of Quality(m/w/x)
Vollzeitmit HomeofficeSeniorGreifswald, Berlin, Binningen - CHEPLAPHARM Arzneimittel GmbH
Global Head of Pharmacovigilance(m/w/x)
Vollzeitmit HomeofficeSeniorGreifswald, Berlin, Binningen - CHEPLAPHARM Arzneimittel GmbH
Global Head of Science Affiliates(m/w/x)
Vollzeitmit HomeofficeSeniorGreifswald, Berlin, Binningen