Die KI-Suchmaschine für Jobs
Senior QA Automation Specialist(m/w/x)
Beschreibung
In this role, you will collaborate with internal teams on quality assurance for electronic batch records, ensuring compliance and consistency. Daily activities will involve reviewing batch records, managing performance metrics, and supporting the QA department to maintain high-quality standards.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •Academic degree in Chemistry, Biotechnology, Life Sciences, or related field
- •Solid experience in GMP-regulated pharmaceutical/API industry
- •Experience in electronic batch records (execution and/or review)
- •Ability to recognize non-compliance and gaps in quality standards
- •Structured, detailed, and well-organized work attitude; open-minded to new ideas; agile, highly motivated, and dynamic
- •Business fluent English; good German language skills advantageous
Ausbildung
Berufserfahrung
ca. 4 - 6 Jahre
Aufgaben
- •Partner with internal customers on quality topics related to eBR setup
- •Check and approve master production records for consistency
- •Review completed batch records within specified timeframes
- •Review minor deviations, investigations, and CAPAs by due dates
- •Ensure closure and archiving of batch records after completion
- •Assist in managing and tracking performance metrics and quality data
- •Support QA department in various meetings
- •Take on additional tasks as assigned
Sprachen
Englisch – verhandlungssicher
Deutsch – Grundkenntnisse
Benefits
Boni & Prämien
- •Compensation programs that recognize high performance
Mitarbeiterrabatte
- •Numerous lifestyle benefits
- •Leisure benefits
Familienfreundlichkeit
- •Family benefits
Sonstige Vorteile
- •Relocation assistance
- CH12 Lonza AGVollzeitnur vor OrtKeine AngabeVisp
- CH12 Lonza AG
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Senior QA Automation Specialist(m/w/x)
Die KI-Suchmaschine für Jobs
Beschreibung
In this role, you will collaborate with internal teams on quality assurance for electronic batch records, ensuring compliance and consistency. Daily activities will involve reviewing batch records, managing performance metrics, and supporting the QA department to maintain high-quality standards.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •Academic degree in Chemistry, Biotechnology, Life Sciences, or related field
- •Solid experience in GMP-regulated pharmaceutical/API industry
- •Experience in electronic batch records (execution and/or review)
- •Ability to recognize non-compliance and gaps in quality standards
- •Structured, detailed, and well-organized work attitude; open-minded to new ideas; agile, highly motivated, and dynamic
- •Business fluent English; good German language skills advantageous
Ausbildung
Berufserfahrung
ca. 4 - 6 Jahre
Aufgaben
- •Partner with internal customers on quality topics related to eBR setup
- •Check and approve master production records for consistency
- •Review completed batch records within specified timeframes
- •Review minor deviations, investigations, and CAPAs by due dates
- •Ensure closure and archiving of batch records after completion
- •Assist in managing and tracking performance metrics and quality data
- •Support QA department in various meetings
- •Take on additional tasks as assigned
Sprachen
Englisch – verhandlungssicher
Deutsch – Grundkenntnisse
Benefits
Boni & Prämien
- •Compensation programs that recognize high performance
Mitarbeiterrabatte
- •Numerous lifestyle benefits
- •Leisure benefits
Familienfreundlichkeit
- •Family benefits
Sonstige Vorteile
- •Relocation assistance
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.
- CH12 Lonza AG
QA Automation Specialist - Batch Record Review(m/w/x)
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