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.Manager Global Quality Assurance CSV(m/w/x)
Global validation of computerized systems for a biotechnology firm, ensuring GxP compliance. 3+ years of CSV/CSA and Data Integrity experience required. Flexible hours, vacation account, digital learning.
Anforderungen
- Degree in pharmacy, chemistry, biology, or related scientific field, or equivalent industrial qualification and experience
- At least 3 years of experience in Quality Assurance, particularly in Computer System Validation (CSV) / Computer System Assurance (CSA) and Data Integrity
- Solid understanding of GxP regulations and pharmaceutical quality systems, with experience in global and local project environments
- Hands-on experience in validation of systems like SAP, Laboratory Information Systems (LIMS), and Manufacturing Execution Systems (MES)
- First audit experience and strong analytical and proactive capabilities, as well as strong problem-solving skills to effectively drive quality improvements
- Motivation to work in an agile environment, embracing change and continuous improvement
- Analytical and proactive, with strong problem-solving skills to drive quality improvements effectively
- Fluent in English
Aufgaben
- Support global validation of computerized systems
- Ensure corporate systems meet quality and regulatory standards
- Oversee pharmaceutical quality system processes
- Collaborate between global and local levels
- Develop and maintain CSV-related quality processes
- Ensure compliance with regulatory requirements
- Contribute to audit and inspection readiness
- Present global QA oversight and validation activities
Berufserfahrung
- 3 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – fließend
- Deutsch – Grundkenntnisse
Tools & Technologien
- SAP
- LIMS
- MES
- GxP
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
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.Manager Global Quality Assurance CSV(m/w/x)
Global validation of computerized systems for a biotechnology firm, ensuring GxP compliance. 3+ years of CSV/CSA and Data Integrity experience required. Flexible hours, vacation account, digital learning.
Anforderungen
- Degree in pharmacy, chemistry, biology, or related scientific field, or equivalent industrial qualification and experience
- At least 3 years of experience in Quality Assurance, particularly in Computer System Validation (CSV) / Computer System Assurance (CSA) and Data Integrity
- Solid understanding of GxP regulations and pharmaceutical quality systems, with experience in global and local project environments
- Hands-on experience in validation of systems like SAP, Laboratory Information Systems (LIMS), and Manufacturing Execution Systems (MES)
- First audit experience and strong analytical and proactive capabilities, as well as strong problem-solving skills to effectively drive quality improvements
- Motivation to work in an agile environment, embracing change and continuous improvement
- Analytical and proactive, with strong problem-solving skills to drive quality improvements effectively
- Fluent in English
Aufgaben
- Support global validation of computerized systems
- Ensure corporate systems meet quality and regulatory standards
- Oversee pharmaceutical quality system processes
- Collaborate between global and local levels
- Develop and maintain CSV-related quality processes
- Ensure compliance with regulatory requirements
- Contribute to audit and inspection readiness
- Present global QA oversight and validation activities
Berufserfahrung
- 3 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – fließend
- Deutsch – Grundkenntnisse
Tools & Technologien
- SAP
- LIMS
- MES
- GxP
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
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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Manager SAP Master Data and Data Quality(m/w/x)
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Specialist QA Compliance(m/w/x)
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