CHEPLAPHARM Arzneimittel GmbH
Global Head of Pharmacovigilance(m/w/x)
Vollzeitmit HomeofficeSenior
Greifswald, Berlin, Binningen
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CHCHEPLAPHARM Arzneimittel GmbH
Senior Portfolio Owner Pharmacovigilance(m/w/x)
Greifswald, Berlin, Binningen
Vollzeitmit HomeofficeSenior
Nejo KI-Zusammenfassung
End-to-end ownership of pharmacovigilance product strategy for global pharmaceutical brand availability. 8+ years in pharmacovigilance and 10+ years leadership experience required. Work from EU country (2 months/year), 30 days holiday.
Anforderungen
- Master’s degree in scientific or related discipline
- 10+ years professional and leadership experience in complex, matrixed, cross-functional organizations
- 8+ years professional experience in Pharmacovigilance
- Proven ability to lead teams in complex environments
- Effective coordination across departments and stakeholders
- Strong leadership and communication skills
- Ability to motivate teams and build relationships
- Ability to evaluate solution approaches
- Work within partially defined frameworks
- Develop robust concepts based on market practices
- Experience handling complex, uncertain problem situations
- Decision-making based on incomplete information
- High degree of autonomy in adapting processes
- Achieve operational and strategic objectives
Aufgaben
- Provide end-to-end ownership of pharmacovigilance product-related activities
- Ensure strong product strategy for compliance, availability, and patient safety
- Act as central point of accountability and escalation
- Coordinate operations and provide leadership to the product team
- Organize and prioritize work
- Foster cross-functional alignment
- Involve relevant experts when needed
- Ensure effective collaboration and high-quality outcomes
- Manage core pharmacovigilance activities
- Process cases and assess causality and labeledness
- Detect signals and evaluate safety
- Mitigate risks and manage crises
- Implement risk management measures
- Deliver regulatory requirements (e.g., PSURs, safety variations)
- Align with global GVP requirements
- Define and drive global product safety strategy
- Integrate safety insights into product lifecycle
- Ensure regulatory PV compliance
- Prepare for inspections
- Align with global health authority expectations
- Provide disciplinary and functional leadership to PV team
- Allocate resources and manage budget
- Prioritize tasks and develop capabilities
- Make final decisions
- Align with internal stakeholders (e.g., SCM, Therapeutic Areas, Quality, Regulatory)
- Act as central escalation point (SPOC)
- Manage external partners, vendors, and service providers
- Monitor global regulatory developments
- Evaluate new PV tools and processes
- Drive continuous improvement of safety systems and methodologies
- Collaborate with medical and scientific functions
Berufserfahrung
- 10 Jahre
Ausbildung
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
Benefits
Flexibles Arbeiten
- Customizable working models
- Working time account
Workation & Sabbatical
- Work from EU country (2 months/year)
Mehr Urlaubstage
- Compensatory time off
- 30 days of holiday
Sonstige Zulagen
- Flexible benefits budget
- Subsidies for meal costs
Betriebliche Altersvorsorge
- Increased company pension provision
Gesundheits- & Fitnessangebote
- Fitness and health offers
Öffi Tickets
- Subsidies for travel costs
Mitarbeiterrabatte
- Corporate benefits platform with discounts
Weiterbildungsangebote
- Tailored 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.
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CHCHEPLAPHARM Arzneimittel GmbH
Senior Portfolio Owner Pharmacovigilance(m/w/x)
Greifswald, Berlin, Binningen
Vollzeitmit HomeofficeSenior
Nejo KI-Zusammenfassung
End-to-end ownership of pharmacovigilance product strategy for global pharmaceutical brand availability. 8+ years in pharmacovigilance and 10+ years leadership experience required. Work from EU country (2 months/year), 30 days holiday.
Anforderungen
- Master’s degree in scientific or related discipline
- 10+ years professional and leadership experience in complex, matrixed, cross-functional organizations
- 8+ years professional experience in Pharmacovigilance
- Proven ability to lead teams in complex environments
- Effective coordination across departments and stakeholders
- Strong leadership and communication skills
- Ability to motivate teams and build relationships
- Ability to evaluate solution approaches
- Work within partially defined frameworks
- Develop robust concepts based on market practices
- Experience handling complex, uncertain problem situations
- Decision-making based on incomplete information
- High degree of autonomy in adapting processes
- Achieve operational and strategic objectives
Aufgaben
- Provide end-to-end ownership of pharmacovigilance product-related activities
- Ensure strong product strategy for compliance, availability, and patient safety
- Act as central point of accountability and escalation
- Coordinate operations and provide leadership to the product team
- Organize and prioritize work
- Foster cross-functional alignment
- Involve relevant experts when needed
- Ensure effective collaboration and high-quality outcomes
- Manage core pharmacovigilance activities
- Process cases and assess causality and labeledness
- Detect signals and evaluate safety
- Mitigate risks and manage crises
- Implement risk management measures
- Deliver regulatory requirements (e.g., PSURs, safety variations)
- Align with global GVP requirements
- Define and drive global product safety strategy
- Integrate safety insights into product lifecycle
- Ensure regulatory PV compliance
- Prepare for inspections
- Align with global health authority expectations
- Provide disciplinary and functional leadership to PV team
- Allocate resources and manage budget
- Prioritize tasks and develop capabilities
- Make final decisions
- Align with internal stakeholders (e.g., SCM, Therapeutic Areas, Quality, Regulatory)
- Act as central escalation point (SPOC)
- Manage external partners, vendors, and service providers
- Monitor global regulatory developments
- Evaluate new PV tools and processes
- Drive continuous improvement of safety systems and methodologies
- Collaborate with medical and scientific functions
Berufserfahrung
- 10 Jahre
Ausbildung
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
Benefits
Flexibles Arbeiten
- Customizable working models
- Working time account
Workation & Sabbatical
- Work from EU country (2 months/year)
Mehr Urlaubstage
- Compensatory time off
- 30 days of holiday
Sonstige Zulagen
- Flexible benefits budget
- Subsidies for meal costs
Betriebliche Altersvorsorge
- Increased company pension provision
Gesundheits- & Fitnessangebote
- Fitness and health offers
Öffi Tickets
- Subsidies for travel costs
Mitarbeiterrabatte
- Corporate benefits platform with discounts
Weiterbildungsangebote
- Tailored 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.
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
Global Head of Pharmacovigilance(m/w/x)
Vollzeitmit HomeofficeSeniorGreifswald, Berlin, Binningen - CHEPLAPHARM Arzneimittel GmbH
Senior Portfolio Owner Regulatory Affairs(m/w/x)
Vollzeitmit HomeofficeSeniorGreifswald, Berlin, Binningen - CHEPLAPHARM Arzneimittel GmbH
Senior Portfolio Owner Quality(m/w/x)
Vollzeitmit HomeofficeSeniorGreifswald, Berlin, Binningen - CHEPLAPHARM Arzneimittel GmbH
Global Head of Product Operations(m/w/x)
Vollzeitmit HomeofficeSeniorGreifswald, Berlin, Binningen - CHEPLAPHARM Arzneimittel GmbH
Global Head of Knowledge Hub(m/w/x)
Vollzeitmit HomeofficeSeniorGreifswald, Berlin, Binningen