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QA Specialist, Batch Record Review(m/w/x)
Reviewing executed batch records and production documentation for pharmaceutical batch releases. Degree in Biology, Chemistry, Biotechnology, or related field, with GMP pharmaceutical experience preferred. Relocation assistance.
Anforderungen
- Degree in Biology, Chemistry, Biotechnology, or related field
- Advantageous experience in GMP pharmaceutical or API industry
- Ability to identify non-compliance and quality gaps
- Structured, precise, and well-organized working attitude
- Openness to new ideas and suggestions
- Agile, highly motivated, and dynamic drive
- Business fluent English
- Preferred good command of German
Aufgaben
- Review executed batch records and production documentation
- Examine test procedures, raw data, and logbooks
- Ensure documentation completeness to support batch releases
- Evaluate batch record comments with operations and QA managers
- Support deviations and investigations for review observations
- Collect and evaluate regular KPI data
- Write and revise SOPs within your area of expertise
- Collaborate with quality and operations functions
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
- Deutsch – verhandlungssicher
Tools & Technologien
- GMP
- API
Benefits
Boni & Prämien
- High performance compensation programs
Karriere- und Weiterentwicklung
- Agile career
Lockere Unternehmenskultur
- Dynamic working culture
Sinnstiftende Arbeit
- Inclusive and ethical workplace
Sonstige Vorteile
- Relocation assistance
Noch nicht perfekt?
- CH12 Lonza AGVollzeitnur vor OrtKeine AngabeVisp
- Lonza
(Senior) QA Operations Specialist, Small Molecules (Large Scale)(m/w/x)
Vollzeitnur vor OrtJuniorVisp - Lonza
Senior Batch Record Reviewer(m/w/x)
Vollzeitnur vor OrtSeniorVisp - Lonza
Senior QA Automation Specialist(m/w/x)
Vollzeitnur vor OrtSeniorVisp - Lonza
QA Batch Record Reviewer, Microbial(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp
QA Specialist, Batch Record Review(m/w/x)
Reviewing executed batch records and production documentation for pharmaceutical batch releases. Degree in Biology, Chemistry, Biotechnology, or related field, with GMP pharmaceutical experience preferred. Relocation assistance.
Anforderungen
- Degree in Biology, Chemistry, Biotechnology, or related field
- Advantageous experience in GMP pharmaceutical or API industry
- Ability to identify non-compliance and quality gaps
- Structured, precise, and well-organized working attitude
- Openness to new ideas and suggestions
- Agile, highly motivated, and dynamic drive
- Business fluent English
- Preferred good command of German
Aufgaben
- Review executed batch records and production documentation
- Examine test procedures, raw data, and logbooks
- Ensure documentation completeness to support batch releases
- Evaluate batch record comments with operations and QA managers
- Support deviations and investigations for review observations
- Collect and evaluate regular KPI data
- Write and revise SOPs within your area of expertise
- Collaborate with quality and operations functions
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
- Deutsch – verhandlungssicher
Tools & Technologien
- GMP
- API
Benefits
Boni & Prämien
- High performance compensation programs
Karriere- und Weiterentwicklung
- Agile career
Lockere Unternehmenskultur
- Dynamic working culture
Sinnstiftende Arbeit
- Inclusive and ethical workplace
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.
Noch nicht perfekt?
- CH12 Lonza AG
QA Automation Specialist - Batch Record Review(m/w/x)
Vollzeitnur vor OrtKeine AngabeVisp - Lonza
(Senior) QA Operations Specialist, Small Molecules (Large Scale)(m/w/x)
Vollzeitnur vor OrtJuniorVisp - Lonza
Senior Batch Record Reviewer(m/w/x)
Vollzeitnur vor OrtSeniorVisp - Lonza
Senior QA Automation Specialist(m/w/x)
Vollzeitnur vor OrtSeniorVisp - Lonza
QA Batch Record Reviewer, Microbial(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp