Dein persönlicher KI-Karriere-Agent
Scientist im Bereich Quality Assurance Operations(m/w/x)
Ensuring GMP compliance for active substance manufacturing and QC testing. Approx. 8 years QA experience in biotech required. Friendly, collaborative culture, personal initiative recognition.
Anforderungen
- Scientific degree (e.g., Biotechnology, Pharmacy, Chemistry, or similar)
- Approx. 8 years QA experience in pharmaceutical/biotech company
- IT experience with TrackWise, MS Office, and databases desirable
- Teamwork, responsibility, and quality awareness
- Very good German and English skills
- Valid work permit
Aufgaben
- Ensure GMP compliance during manufacturing, QC testing, and release of active substances
- Design and implement GMP-compliant quality management systems
- Adapt systems to new laws and guidelines
- Conduct management reviews and regular KPI reporting
- Manage documentation, including harmonizing QS systems across AGC Biologics sites
- Qualify suppliers, including audits and negotiating quality agreements
- Support customer audits and regulatory inspections
- Provide QA support for qualifications and validations
- Review batch records and prepare batch release
- Process deviations, OOS results, and change control procedures
- Follow up on CAPA actions
- Contribute to all QA activities in a pharmaceutical operation
Berufserfahrung
- 8 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Deutsch – fließend
- Englisch – verhandlungssicher
Tools & Technologien
- TrackWise
- MS Office
Benefits
Attraktive Vergütung
- Highly competitive compensation package
Lockere Unternehmenskultur
- Friendly, collaborative culture
Sonstige Vorteile
- Personal initiative recognition
Karriere- und Weiterentwicklung
- Professional achievement recognition
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Scientist im Bereich Quality Assurance Operations(m/w/x)
Ensuring GMP compliance for active substance manufacturing and QC testing. Approx. 8 years QA experience in biotech required. Friendly, collaborative culture, personal initiative recognition.
Anforderungen
- Scientific degree (e.g., Biotechnology, Pharmacy, Chemistry, or similar)
- Approx. 8 years QA experience in pharmaceutical/biotech company
- IT experience with TrackWise, MS Office, and databases desirable
- Teamwork, responsibility, and quality awareness
- Very good German and English skills
- Valid work permit
Aufgaben
- Ensure GMP compliance during manufacturing, QC testing, and release of active substances
- Design and implement GMP-compliant quality management systems
- Adapt systems to new laws and guidelines
- Conduct management reviews and regular KPI reporting
- Manage documentation, including harmonizing QS systems across AGC Biologics sites
- Qualify suppliers, including audits and negotiating quality agreements
- Support customer audits and regulatory inspections
- Provide QA support for qualifications and validations
- Review batch records and prepare batch release
- Process deviations, OOS results, and change control procedures
- Follow up on CAPA actions
- Contribute to all QA activities in a pharmaceutical operation
Berufserfahrung
- 8 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Deutsch – fließend
- Englisch – verhandlungssicher
Tools & Technologien
- TrackWise
- MS Office
Benefits
Attraktive Vergütung
- Highly competitive compensation package
Lockere Unternehmenskultur
- Friendly, collaborative culture
Sonstige Vorteile
- Personal initiative recognition
Karriere- und Weiterentwicklung
- Professional achievement recognition
Gefällt dir diese Stelle?
BetaDein Career Agent findet täglich ähnliche Jobs für dich.
Über das Unternehmen
AGC Biologics GmbH
Branche
Pharmaceuticals
Beschreibung
AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) committed to delivering high standards of service.
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