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Senior QA Specialist, QA Operations(m/w/x)
Overseeing quality operations for commissioning and qualification at global life sciences firm, coordinating with QC, Engineering, and Manufacturing. Significant experience in pharmaceutical quality required; tech transfer experience preferred. Relocation assistance available.
Anforderungen
- Academic degree in Life Sciences or related field
- Significant experience in pharmaceutical Quality area
- Work experience in Quality Assurance, Production or Engineering in pharmaceutical industries and cGMP regulated environment
- Preferred QA experience in tech transfer
- Excellent knowledge of computer systems and quality tools such as risk based approaches
- Fluent English (written and verbal)
Aufgaben
- Manage QA operations during commissioning and qualification
- Assess and manage tasks impacting quality during GMP manufacturing
- Plan future activities and coordinate with QC, Engineering, and Manufacturing
- Support daily Quality Assurance activities per approved SOPs and policies
- Review GMP records for compliance with cGMP procedures
- Make real-time decisions on process events based on SOPs and policies
- Participate in walkthroughs and audits/inspections
Berufserfahrung
- ca. 4 - 6 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- TW
- SAP
Benefits
Sonstige Vorteile
- Lifestyle benefits
- Relocation assistance
Familienfreundlichkeit
- Family benefits
Mitarbeiterrabatte
- Leisure benefits
Noch nicht perfekt?
- CH12 Lonza AGVollzeitnur vor OrtSeniorVisp
- Lonza
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Senior QA Specialist, QA Operations(m/w/x)
Overseeing quality operations for commissioning and qualification at global life sciences firm, coordinating with QC, Engineering, and Manufacturing. Significant experience in pharmaceutical quality required; tech transfer experience preferred. Relocation assistance available.
Anforderungen
- Academic degree in Life Sciences or related field
- Significant experience in pharmaceutical Quality area
- Work experience in Quality Assurance, Production or Engineering in pharmaceutical industries and cGMP regulated environment
- Preferred QA experience in tech transfer
- Excellent knowledge of computer systems and quality tools such as risk based approaches
- Fluent English (written and verbal)
Aufgaben
- Manage QA operations during commissioning and qualification
- Assess and manage tasks impacting quality during GMP manufacturing
- Plan future activities and coordinate with QC, Engineering, and Manufacturing
- Support daily Quality Assurance activities per approved SOPs and policies
- Review GMP records for compliance with cGMP procedures
- Make real-time decisions on process events based on SOPs and policies
- Participate in walkthroughs and audits/inspections
Berufserfahrung
- ca. 4 - 6 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- TW
- SAP
Benefits
Sonstige Vorteile
- Lifestyle benefits
- Relocation assistance
Familienfreundlichkeit
- Family benefits
Mitarbeiterrabatte
- Leisure benefits
Über das Unternehmen
Lonza
Branche
Pharmaceuticals
Beschreibung
Lonza is a global leader in life sciences, committed to improving lives through innovative solutions and ethical practices.
Noch nicht perfekt?
- CH12 Lonza AG
Senior QA Specialist(m/w/x)
Vollzeitnur vor OrtSeniorVisp - Lonza
Senior QA Specialist/QA Project Manager(m/w/x)
Vollzeitnur vor OrtSeniorVisp - CH12 Lonza AG
Senior QA Specialist, QA Project Management(m/w/x)
Vollzeitnur vor OrtSeniorVisp - Lonza
Senior QA Specialist, DPS (Drug Product Services)(m/w/x)
Vollzeitnur vor OrtSeniorVisp - Lonza
Senior QA Specialist - Qualification/Validation/EM (Environmental Monitoring)(m/w/x)
Vollzeitnur vor OrtSeniorVisp