BioNTech SE
Senior Director Global Quality Supply(m/w/x)
Vollzeitnur vor OrtSenior
Mainz
Neuer Job?Nejo!
Dein persönlicher KI-Karriere-Agent
BIBioNTech SE
Executive Director Manufacturing Network QA(m/w/x)
Mainz
VollzeitVor OrtSenior
Nejo KI-Zusammenfassung
Overseeing GxP-compliant pharmaceutical manufacturing operations globally and aligning with clinical objectives. Extensive GxP and pharmaceutical manufacturing experience required. Flexible hours, vacation account, digital learning.
Anforderungen
- Degree in Life Sciences, Pharmacy, Chemistry, Engineering, or related field
- Advanced degrees (MSc, PhD, MBA) desirable
- Extensive Quality Assurance experience
- Extensive GxP compliance experience
- Extensive manufacturing operations experience (pharmaceutical)
- Proven track record managing global manufacturing networks
- Proven track record leading large-scale strategic initiatives
- Significant experience steering external manufacturing networks
- Experience managing external manufacturing partnerships
- Experience ensuring compliance across diverse modalities
- Demonstrated success preparing commercial product launches (QA perspective)
- Demonstrated success executing commercial product launches (QA perspective)
- Familiarity with international regulatory landscapes
- Familiarity with manufacturing operations (China, Singapore, Europe, USA)
- Strong leadership capabilities
- Ability to inspire cross-functional teams
- Ability to guide cross-functional teams (diverse regions/modalities)
- Direct disciplinary team management
- Exceptional analytical skills
- Exceptional problem-solving skills
- Ability to manage escalations
- Ability to drive effective remediation strategies
- Excellent communication skills
- Excellent interpersonal skills
- Ability to collaborate effectively with stakeholders
Aufgaben
- Oversee GxP-compliant manufacturing operations globally
- Align operations with clinical and commercial objectives
- Drive strategic and tactical changes across the network
- Manage escalations and remediation activities
- Represent Quality Assurance in critical decision-making forums
- Ensure site-specific compliance with regional and global standards
- Prepare for internal and external manufacturing decision forums
- Lead a team of Site Quality Heads and Quality Assurance professionals
- Foster a culture of collaboration, accountability, and excellence
- Equip the team with necessary skills and resources
- Drive continuous improvement in team performance
Berufserfahrung
- ca. 4 - 6 Jahre
Ausbildung
- Bachelor-AbschlussODER
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
Benefits
Flexibles Arbeiten
- Flexible hours
Mehr Urlaubstage
- Vacation account
Weiterbildungsangebote
- Digital Learning
- LinkedIn Learning
Karriere- und Weiterentwicklung
- Performance and talent development
- Leadership development
Sonstige Vorteile
- Apprenticeships
- Support for your full potential
Startup-Atmosphäre
- Voice at the table
Lockere Unternehmenskultur
- Culture on an equal footing
Sinnstiftende Arbeit
- Opportunities to shape and impact
Firmenfahrrad
- Company bike
Öffi Tickets
- Job ticket
- Deutschlandticket
Betriebliche Altersvorsorge
- Employer-funded pension
Kinderbetreuung
- Childcare
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens BioNTech SE 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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Overseeing GxP-compliant pharmaceutical manufacturing operations globally and aligning with clinical objectives. Extensive GxP and pharmaceutical manufacturing experience required. Flexible hours, vacation account, digital learning.
Anforderungen
- Degree in Life Sciences, Pharmacy, Chemistry, Engineering, or related field
- Advanced degrees (MSc, PhD, MBA) desirable
- Extensive Quality Assurance experience
- Extensive GxP compliance experience
- Extensive manufacturing operations experience (pharmaceutical)
- Proven track record managing global manufacturing networks
- Proven track record leading large-scale strategic initiatives
- Significant experience steering external manufacturing networks
- Experience managing external manufacturing partnerships
- Experience ensuring compliance across diverse modalities
- Demonstrated success preparing commercial product launches (QA perspective)
- Demonstrated success executing commercial product launches (QA perspective)
- Familiarity with international regulatory landscapes
- Familiarity with manufacturing operations (China, Singapore, Europe, USA)
- Strong leadership capabilities
- Ability to inspire cross-functional teams
- Ability to guide cross-functional teams (diverse regions/modalities)
- Direct disciplinary team management
- Exceptional analytical skills
- Exceptional problem-solving skills
- Ability to manage escalations
- Ability to drive effective remediation strategies
- Excellent communication skills
- Excellent interpersonal skills
- Ability to collaborate effectively with stakeholders
Aufgaben
- Oversee GxP-compliant manufacturing operations globally
- Align operations with clinical and commercial objectives
- Drive strategic and tactical changes across the network
- Manage escalations and remediation activities
- Represent Quality Assurance in critical decision-making forums
- Ensure site-specific compliance with regional and global standards
- Prepare for internal and external manufacturing decision forums
- Lead a team of Site Quality Heads and Quality Assurance professionals
- Foster a culture of collaboration, accountability, and excellence
- Equip the team with necessary skills and resources
- Drive continuous improvement in team performance
Berufserfahrung
- ca. 4 - 6 Jahre
Ausbildung
- Bachelor-AbschlussODER
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
Benefits
Flexibles Arbeiten
- Flexible hours
Mehr Urlaubstage
- Vacation account
Weiterbildungsangebote
- Digital Learning
- LinkedIn Learning
Karriere- und Weiterentwicklung
- Performance and talent development
- Leadership development
Sonstige Vorteile
- Apprenticeships
- Support for your full potential
Startup-Atmosphäre
- Voice at the table
Lockere Unternehmenskultur
- Culture on an equal footing
Sinnstiftende Arbeit
- Opportunities to shape and impact
Firmenfahrrad
- Company bike
Öffi Tickets
- Job ticket
- Deutschlandticket
Betriebliche Altersvorsorge
- Employer-funded pension
Kinderbetreuung
- Childcare
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens BioNTech SE 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
BioNTech SE
Branche
Pharmaceuticals
Beschreibung
Das Unternehmen entwickelt bahnbrechende Medikamente zur Verbesserung der globalen Gesundheit und zur Bekämpfung von Krankheiten.
Noch nicht perfekt?
- BioNTech SE
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Vollzeitnur vor OrtSeniorMainz - BioNTech SE
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Vollzeitnur vor OrtSeniorMainz - BioNTech SE
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Vollzeitnur vor OrtBerufserfahrenMainz - BioNTech SE
.Manager Global Quality Assurance CSV(m/w/x)
Vollzeitnur vor OrtBerufserfahrenMainz - BioNTech SE
Senior Scientist Manufacturing(m/w/x)
Vollzeitnur vor OrtSeniorMainz