Dein persönlicher KI-Karriere-Agent
Qualification Validation Expert(m/w/x)
Qualifying and validating production, QC, and logistics systems for biomedical tech. GMP and FDA guideline familiarity required. Flexible remote work, international teams.
Anforderungen
- Degree in life sciences, engineering, or comparable technical field, or similar qualification
- Familiarity with GMP and FDA guidelines
- Hands-on experience qualifying systems in regulated environments (pharmaceutical industry or similar)
- Ability to bring structure to dynamic environments
- Initiative in process improvement
- Team player with open communication skills
- Fluent English
- Comfortable collaborating across functions and cultures
Aufgaben
- Support transition from clinical to commercial manufacturing
- Ensure compliance with GMP standards
- Plan and execute qualification and validation
- Manage lifecycle of production, quality control, and logistics systems
- Prepare and maintain qualification and validation documentation
- Advise on qualification and validation projects
- Propose and implement pragmatic solutions
- Contribute to GxP activities
- Enhance qualification and validation processes
- Collaborate with internal and external stakeholders
- Conduct training sessions for knowledge transfer
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Abgeschlossene BerufsausbildungODER
- Bachelor-Abschluss
Sprachen
- Englisch – fließend
Benefits
Flexibles Arbeiten
- Flexible and remote work
Lockere Unternehmenskultur
- International teams
- Cross-border intercultural communication
- Room for creativity
Gesundheits- & Fitnessangebote
- Corporate sports activities
- Health provision
Weiterbildungsangebote
- In-house Training Academy
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Qualification Validation Expert(m/w/x)
Qualifying and validating production, QC, and logistics systems for biomedical tech. GMP and FDA guideline familiarity required. Flexible remote work, international teams.
Anforderungen
- Degree in life sciences, engineering, or comparable technical field, or similar qualification
- Familiarity with GMP and FDA guidelines
- Hands-on experience qualifying systems in regulated environments (pharmaceutical industry or similar)
- Ability to bring structure to dynamic environments
- Initiative in process improvement
- Team player with open communication skills
- Fluent English
- Comfortable collaborating across functions and cultures
Aufgaben
- Support transition from clinical to commercial manufacturing
- Ensure compliance with GMP standards
- Plan and execute qualification and validation
- Manage lifecycle of production, quality control, and logistics systems
- Prepare and maintain qualification and validation documentation
- Advise on qualification and validation projects
- Propose and implement pragmatic solutions
- Contribute to GxP activities
- Enhance qualification and validation processes
- Collaborate with internal and external stakeholders
- Conduct training sessions for knowledge transfer
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Abgeschlossene BerufsausbildungODER
- Bachelor-Abschluss
Sprachen
- Englisch – fließend
Benefits
Flexibles Arbeiten
- Flexible and remote work
Lockere Unternehmenskultur
- International teams
- Cross-border intercultural communication
- Room for creativity
Gesundheits- & Fitnessangebote
- Corporate sports activities
- Health provision
Weiterbildungsangebote
- In-house Training Academy
Gefällt dir diese Stelle?
BetaDein Career Agent findet täglich ähnliche Jobs für dich.
Über das Unternehmen
Miltenyi Biotec
Branche
Pharmaceuticals
Beschreibung
Das Unternehmen entwickelt einzigartige Lösungen für die biomedizinische Spitzenforschung sowie neuartige Zell- und Gentherapien.
Noch nicht perfekt?
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