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CQV Engineer / Qualification & Validation Engineer(m/w/x)
Developing commissioning and qualification documents for new plants and critical systems in life sciences, managing GEP/GMP changes. Proven experience in regulated GMP environment required; COMOS, DMS, Kneat, TrackWise, SAP familiarity advantageous. Flexible work arrangements.
Anforderungen
- Graduation from a technical school or university degree
- Proven experience in a regulated GMP environment
- Strong proficiency in MS Office; familiarity with COMOS, DMS, Kneat, TrackWise, and SAP advantageous
- Proficiency in written and spoken German and/or English
- Independent and flexible work habits; excellent communication skills
- Openness to new ideas; agility in thinking; proactivity in problem-solving
Aufgaben
- Develop and maintain commissioning and qualification documents for new plants
- Create PQs for critical systems
- Provide ongoing SLC support post-implementation
- Supervise and resolve deviations
- Manage changes related to GEP and GMP
- Implement CAPAs effectively
- Coordinate efforts between internal teams and external service providers
- Ensure seamless project execution
- Present qualification documents during audits and inspections
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Abgeschlossene BerufsausbildungODER
- Bachelor-Abschluss
Sprachen
- Deutsch – verhandlungssicher
- Englisch – verhandlungssicher
Tools & Technologien
- MS Office
- COMOS
- DMS
- Kneat
- TrackWise
- SAP
Benefits
Boni & Prämien
- Compensation programs that recognize high performance
Mitarbeiterrabatte
- Numerous lifestyle benefits
- Leisure benefits
Familienfreundlichkeit
- Family benefits
Karriere- und Weiterentwicklung
- Agile career
Lockere Unternehmenskultur
- Dynamic work culture
- Inclusive workplace
Sonstige Vorteile
- Relocation assistance
Noch nicht perfekt?
- LonzaVollzeitnur vor OrtBerufserfahrenVisp
- CH12 Lonza AG
CQV Ingenieur / Qualifizierungs- und Validierungsspezialist(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp - CH12 Lonza AG
Qualifizierungsspezialist CQV(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp - CH12 Lonza AG
(Senior) QA Qualification Specialist(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp - CH12 Lonza AG
CSV Engineer(m/w/x)
Vollzeitnur vor OrtSeniorVisp
CQV Engineer / Qualification & Validation Engineer(m/w/x)
Developing commissioning and qualification documents for new plants and critical systems in life sciences, managing GEP/GMP changes. Proven experience in regulated GMP environment required; COMOS, DMS, Kneat, TrackWise, SAP familiarity advantageous. Flexible work arrangements.
Anforderungen
- Graduation from a technical school or university degree
- Proven experience in a regulated GMP environment
- Strong proficiency in MS Office; familiarity with COMOS, DMS, Kneat, TrackWise, and SAP advantageous
- Proficiency in written and spoken German and/or English
- Independent and flexible work habits; excellent communication skills
- Openness to new ideas; agility in thinking; proactivity in problem-solving
Aufgaben
- Develop and maintain commissioning and qualification documents for new plants
- Create PQs for critical systems
- Provide ongoing SLC support post-implementation
- Supervise and resolve deviations
- Manage changes related to GEP and GMP
- Implement CAPAs effectively
- Coordinate efforts between internal teams and external service providers
- Ensure seamless project execution
- Present qualification documents during audits and inspections
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Abgeschlossene BerufsausbildungODER
- Bachelor-Abschluss
Sprachen
- Deutsch – verhandlungssicher
- Englisch – verhandlungssicher
Tools & Technologien
- MS Office
- COMOS
- DMS
- Kneat
- TrackWise
- SAP
Benefits
Boni & Prämien
- Compensation programs that recognize high performance
Mitarbeiterrabatte
- Numerous lifestyle benefits
- Leisure benefits
Familienfreundlichkeit
- Family benefits
Karriere- und Weiterentwicklung
- Agile career
Lockere Unternehmenskultur
- Dynamic work culture
- Inclusive workplace
Sonstige Vorteile
- Relocation assistance
Über das Unternehmen
CH12 Lonza AG
Branche
Healthcare
Beschreibung
The company is a global leader in life sciences, dedicated to improving lives through innovative solutions.
Noch nicht perfekt?
- Lonza
Qualification CQV Engineer(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp - CH12 Lonza AG
CQV Ingenieur / Qualifizierungs- und Validierungsspezialist(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp - CH12 Lonza AG
Qualifizierungsspezialist CQV(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp - CH12 Lonza AG
(Senior) QA Qualification Specialist(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp - CH12 Lonza AG
CSV Engineer(m/w/x)
Vollzeitnur vor OrtSeniorVisp