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Quality Assurance Manager – Third Party Manufacturing & Technical Transfer(m/w/x)
Leading QA for external pharmaceutical manufacturing, overseeing new product integration and deviation investigations, at a global healthcare solutions provider. 10+ years in pharmaceutical manufacturing and a relevant science degree required; French language skills a plus. Flexible working arrangements.
Anforderungen
- Degree in Pharmacy, Pharmaceutical Technology, Biotechnology, or related field
- 10+ years of experience in pharmaceutical manufacturing
- Strong knowledge of GMP and international quality standards
- Excellent communication skills in English; French is a plus
- Proven leadership and ability to foster collaboration
- Willingness to travel up to 30%
- Expertise in cGMP for solid, liquid, injectable, and biosimilar products
- Certifications such as IRCA Lead Auditor or GMP-GDP training are an advantage
Aufgaben
- Ensure TPMs meet cGMP and regulatory standards
- Develop and implement Quality Improvement Plans
- Drive continuous improvement initiatives
- Monitor quality performance and manage Quality Technical Agreements
- Act as QA lead for deviations and complaints investigations
- Oversee CAPA and product release issues
- Manage validation and change controls
- Coordinate audits and compliance initiatives with TPMs
- Lead QA activities during technology transfers
- Support new product introductions and geographic expansion
- Collaborate across functions to resolve technical issues
Berufserfahrung
- 10 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
- Französisch – Grundkenntnisse
Benefits
Flexibles Arbeiten
- Flexibility
Weiterbildungsangebote
- Development programs
Sonstige Vorteile
- Supportive environment
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Quality Assurance Manager – Third Party Manufacturing & Technical Transfer(m/w/x)
Leading QA for external pharmaceutical manufacturing, overseeing new product integration and deviation investigations, at a global healthcare solutions provider. 10+ years in pharmaceutical manufacturing and a relevant science degree required; French language skills a plus. Flexible working arrangements.
Anforderungen
- Degree in Pharmacy, Pharmaceutical Technology, Biotechnology, or related field
- 10+ years of experience in pharmaceutical manufacturing
- Strong knowledge of GMP and international quality standards
- Excellent communication skills in English; French is a plus
- Proven leadership and ability to foster collaboration
- Willingness to travel up to 30%
- Expertise in cGMP for solid, liquid, injectable, and biosimilar products
- Certifications such as IRCA Lead Auditor or GMP-GDP training are an advantage
Aufgaben
- Ensure TPMs meet cGMP and regulatory standards
- Develop and implement Quality Improvement Plans
- Drive continuous improvement initiatives
- Monitor quality performance and manage Quality Technical Agreements
- Act as QA lead for deviations and complaints investigations
- Oversee CAPA and product release issues
- Manage validation and change controls
- Coordinate audits and compliance initiatives with TPMs
- Lead QA activities during technology transfers
- Support new product introductions and geographic expansion
- Collaborate across functions to resolve technical issues
Berufserfahrung
- 10 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
- Französisch – Grundkenntnisse
Benefits
Flexibles Arbeiten
- Flexibility
Weiterbildungsangebote
- Development programs
Sonstige Vorteile
- Supportive environment
Über das Unternehmen
Abbott
Branche
Healthcare
Beschreibung
Das Unternehmen ist ein weltweit führendes Unternehmen im Gesundheitswesen, das bahnbrechende wissenschaftliche Erkenntnisse nutzt und Lösungen zur Verbesserung der Gesundheit der Menschen entwickelt.
Noch nicht perfekt?
- 1201 F. Hoffmann-La Roche AG
QA Manager(m/w/x)
Vollzeitnur vor OrtSeniorKaiseraugst - 1201 F. Hoffmann-La Roche AG
QA Manager IT/OT(m/w/x)
Vollzeitnur vor OrtSeniorBasel - Roche Pharma AG
QA Manager für das Quality System und Compliance in Central Certification(m/w/x)
VollzeitBefristeter Vertragnur vor OrtBerufserfahrenGrenzach - 1201 F. Hoffmann-La Roche AG
Site Manager External Manufacturing(m/w/x)
Vollzeitnur vor OrtSeniorBasel - F. Hoffmann-La Roche AG
QA Manager - Antibiotics(m/w/x)
VollzeitBefristeter Vertragnur vor OrtSeniorKaiseraugst