CHEPLAPHARM Arzneimittel GmbH
Senior Project Lead End to End Integration(m/w/x)
VollzeitRemoteSenior
Greifswald, Berlin
Neuer Job?Nejo!
Die KI-Suchmaschine für Jobs
CHCHEPLAPHARM Arzneimittel GmbH
Head of Regulatory Affairs(m/w/x)
Greifswald
Vollzeitmit HomeofficeSenior
Nejo KI-Zusammenfassung
Leading regulatory activities for specialty pharma products with a 10-member product team at a global Specialty Pharma company. 10+ years Regulatory Affairs experience and initial leadership required. 30 days holiday, individually customizable working models.
Anforderungen
- Degree in Natural Sciences, Pharmacy or Medicine
- At least 10 years of professional experience in Regulatory Affairs
- Initial leadership experience
- Strong understanding of multidisciplinary functions across the pharmaceutical product lifecycle
- Proven experience in development and leadership of regulatory strategies
- High competence in managing complex interfaces and engaging with stakeholders
- Cooperative and solution-oriented working approach
- Confident communication and negotiation skills in German and English
Aufgaben
- Lead regulatory activities for a product team of up to 10 members
- Ensure compliance with national and international regulations
- Develop and implement regulatory strategies aligned with company goals
- Take responsibility for all regulatory processes within the team
- Ensure timely execution and proactive risk management
- Provide regulatory expertise to internal functions and project teams
- Contribute to the optimization of regulatory processes and systems
- Act as the Regulatory Affairs representative in cross-functional initiatives
- Monitor and assess legislative and regulatory developments
- Evaluate the impact of regulations on the business
- Provide technical leadership and foster team development
- Manage external service providers for quality and compliance
Berufserfahrung
- 10 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Deutsch – verhandlungssicher
- Englisch – verhandlungssicher
Benefits
Flexibles Arbeiten
- Individually customisable working models
Mehr Urlaubstage
- Compensatory time off
- 30 days of holiday
Sonstige Zulagen
- Flexible benefits budget
- Subsidies for travel and meal costs
Gesundheits- & Fitnessangebote
- Fitness and health offers
Mitarbeiterrabatte
- Access to corporate benefits platform
Weiterbildungsangebote
- Internal and external training courses
Team Events & Ausflüge
- Company and 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.
Noch nicht perfekt?
- CHEPLAPHARM Arzneimittel GmbH
Senior Leader SCM Therapeutic Area - Oncology & Dermatology(m/w/x)
Vollzeitmit HomeofficeSeniorGreifswald, Berlin - CHEPLAPHARM Arzneimittel GmbH
Senior Manager External Supply Onboarding(m/w/x)
VollzeitRemoteSeniorGreifswald, Berlin - CHEPLAPHARM Arzneimittel GmbH
Senior Specialist Quality – Systems – Deviation and Change Control Management(m/w/x)
Vollzeitmit HomeofficeSeniorGreifswald - CHEPLAPHARM Arzneimittel GmbH
Senior Portfolio Manager(m/w/x)
Vollzeitmit HomeofficeSeniorGreifswald, Berlin
CHCHEPLAPHARM Arzneimittel GmbH
Head of Regulatory Affairs(m/w/x)
Greifswald
Vollzeitmit HomeofficeSenior
Nejo KI-Zusammenfassung
Leading regulatory activities for specialty pharma products with a 10-member product team at a global Specialty Pharma company. 10+ years Regulatory Affairs experience and initial leadership required. 30 days holiday, individually customizable working models.
Anforderungen
- Degree in Natural Sciences, Pharmacy or Medicine
- At least 10 years of professional experience in Regulatory Affairs
- Initial leadership experience
- Strong understanding of multidisciplinary functions across the pharmaceutical product lifecycle
- Proven experience in development and leadership of regulatory strategies
- High competence in managing complex interfaces and engaging with stakeholders
- Cooperative and solution-oriented working approach
- Confident communication and negotiation skills in German and English
Aufgaben
- Lead regulatory activities for a product team of up to 10 members
- Ensure compliance with national and international regulations
- Develop and implement regulatory strategies aligned with company goals
- Take responsibility for all regulatory processes within the team
- Ensure timely execution and proactive risk management
- Provide regulatory expertise to internal functions and project teams
- Contribute to the optimization of regulatory processes and systems
- Act as the Regulatory Affairs representative in cross-functional initiatives
- Monitor and assess legislative and regulatory developments
- Evaluate the impact of regulations on the business
- Provide technical leadership and foster team development
- Manage external service providers for quality and compliance
Berufserfahrung
- 10 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Deutsch – verhandlungssicher
- Englisch – verhandlungssicher
Benefits
Flexibles Arbeiten
- Individually customisable working models
Mehr Urlaubstage
- Compensatory time off
- 30 days of holiday
Sonstige Zulagen
- Flexible benefits budget
- Subsidies for travel and meal costs
Gesundheits- & Fitnessangebote
- Fitness and health offers
Mitarbeiterrabatte
- Access to corporate benefits platform
Weiterbildungsangebote
- Internal and external training courses
Team Events & Ausflüge
- Company and 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.
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 Project Lead End to End Integration(m/w/x)
VollzeitRemoteSeniorGreifswald, Berlin - CHEPLAPHARM Arzneimittel GmbH
Senior Leader SCM Therapeutic Area - Oncology & Dermatology(m/w/x)
Vollzeitmit HomeofficeSeniorGreifswald, Berlin - CHEPLAPHARM Arzneimittel GmbH
Senior Manager External Supply Onboarding(m/w/x)
VollzeitRemoteSeniorGreifswald, Berlin - CHEPLAPHARM Arzneimittel GmbH
Senior Specialist Quality – Systems – Deviation and Change Control Management(m/w/x)
Vollzeitmit HomeofficeSeniorGreifswald - CHEPLAPHARM Arzneimittel GmbH
Senior Portfolio Manager(m/w/x)
Vollzeitmit HomeofficeSeniorGreifswald, Berlin