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Senior QA Expert - Equipment Qualification & Validation(m/w/x)
Leading qualification of aseptic fill and finish equipment, managing GMP deviations at global life sciences firm. Experience with aseptic fill&finish lines and health authority audits required. Relocation assistance available.
Anforderungen
- Experience with aseptic fill&finish lines
- Experience with equipment qualification and validation
- Experience with health authority audits
- Degree in life science or equivalent
- Teamwork and positive culture contribution
- Experience or interest in data integrity
- Fluency in English and German skills
Aufgaben
- Lead qualification and validation for aseptic fill and finish equipment
- Manage GMP deviations within global quality management systems
- Define qualification strategies for CAPEX and OPEX projects
- Supervise equipment trending and sterilization process validation
- Oversee change control management and CAPA handling
- Serve as subject matter expert during audits and inspections
- Manage the lifecycle of equipment qualification documentation
- Approve SOPs, qualification protocols, and technical reports
Berufserfahrung
- ca. 4 - 6 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
- Deutsch – Grundkenntnisse
Tools & Technologien
- aseptic fill&finish lines
- GMP
- Swissmedic
- FDA
- data integrity (DI)
Benefits
Boni & Prämien
- Performance-based compensation programs
Mitarbeiterrabatte
- Lifestyle benefits
- Leisure benefits
Familienfreundlichkeit
- Family benefits
Sonstige Vorteile
- Relocation assistance
Weiterbildungsangebote
- Agile career opportunities
Startup-Atmosphäre
- Dynamic work culture
Sinnstiftende Arbeit
- Inclusive and ethical workplace
Noch nicht perfekt?
- LonzaVollzeitnur vor OrtBerufserfahrenStein (AR)
- Lonza
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Senior Scientist, Equipment Qualification(m/w/x)
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Vollzeitnur vor OrtSeniorStein (AR)
Senior QA Expert - Equipment Qualification & Validation(m/w/x)
Leading qualification of aseptic fill and finish equipment, managing GMP deviations at global life sciences firm. Experience with aseptic fill&finish lines and health authority audits required. Relocation assistance available.
Anforderungen
- Experience with aseptic fill&finish lines
- Experience with equipment qualification and validation
- Experience with health authority audits
- Degree in life science or equivalent
- Teamwork and positive culture contribution
- Experience or interest in data integrity
- Fluency in English and German skills
Aufgaben
- Lead qualification and validation for aseptic fill and finish equipment
- Manage GMP deviations within global quality management systems
- Define qualification strategies for CAPEX and OPEX projects
- Supervise equipment trending and sterilization process validation
- Oversee change control management and CAPA handling
- Serve as subject matter expert during audits and inspections
- Manage the lifecycle of equipment qualification documentation
- Approve SOPs, qualification protocols, and technical reports
Berufserfahrung
- ca. 4 - 6 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
- Deutsch – Grundkenntnisse
Tools & Technologien
- aseptic fill&finish lines
- GMP
- Swissmedic
- FDA
- data integrity (DI)
Benefits
Boni & Prämien
- Performance-based compensation programs
Mitarbeiterrabatte
- Lifestyle benefits
- Leisure benefits
Familienfreundlichkeit
- Family benefits
Sonstige Vorteile
- Relocation assistance
Weiterbildungsangebote
- Agile career opportunities
Startup-Atmosphäre
- Dynamic work culture
Sinnstiftende Arbeit
- Inclusive and ethical workplace
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?
- Lonza
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Vollzeitnur vor OrtBerufserfahrenStein (AR) - Lonza
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Vollzeitnur vor OrtSeniorStein (AR) - CH12 Lonza AG
Global MSAT Drug Product Qualification and Validation Lead(m/w/x)
Vollzeitnur vor OrtSeniorStein (AR)