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QC Data Reviewer for Biochemical Methods(m/w/x)
Reviewing ELISA and qPCR data, assessing quality parameters for stability studies and batch release. GMP environment experience in Quality Control and hands-on qPCR/ELISA experience required. Performance-based compensation programs.
Anforderungen
- BSc, MSc, or equivalent experience in Chemistry, Biochemistry, or similar field
- Experience in a GMP environment within Quality Control
- Hands-on experience with qPCR and/or ELISA
- Detail-oriented and adaptable to changing priorities
- Knowledge of Quality Management Systems and LIMS
- Fluency in English; language skills in German
Aufgaben
- Review data from ELISA and qPCR analyses
- Check execution of assays in the lab
- Evaluate results for accuracy
- Assess quality parameters for stability studies
- Evaluate batch release quality
- Investigate unexpected results
- Ensure compliance with GMP and internal procedures
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Bachelor-AbschlussODER
- Master-Abschluss
Sprachen
- Englisch – fließend
- Deutsch – Grundkenntnisse
Tools & Technologien
- qPCR
- ELISA
- Quality Management Systems
- LIMS
Benefits
Boni & Prämien
- Compensation programs recognizing high performance
Mitarbeiterrabatte
- Numerous lifestyle benefits
- Leisure benefits
Familienfreundlichkeit
- Family benefits
Karriere- und Weiterentwicklung
- Agile career
Lockere Unternehmenskultur
- Dynamic work culture
- Inclusive workplace
Sinnstiftende Arbeit
- Ethical workplace
Sonstige Vorteile
- Relocation assistance
Noch nicht perfekt?
- LonzaVollzeitnur vor OrtSeniorVisp
- CH12 Lonza AG
QC Laborantin:in(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp - Lonza
QA Specialist, Batch Record Review(m/w/x)
Vollzeitnur vor OrtJuniorVisp - Lonza
QC Deviation & Investigation Specialist(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp - CH12 Lonza AG
Senior Labortechniker QC mit dem Schwerpunkt Bioanalytik(m/w/x)
Vollzeitnur vor OrtSeniorVisp
QC Data Reviewer for Biochemical Methods(m/w/x)
Reviewing ELISA and qPCR data, assessing quality parameters for stability studies and batch release. GMP environment experience in Quality Control and hands-on qPCR/ELISA experience required. Performance-based compensation programs.
Anforderungen
- BSc, MSc, or equivalent experience in Chemistry, Biochemistry, or similar field
- Experience in a GMP environment within Quality Control
- Hands-on experience with qPCR and/or ELISA
- Detail-oriented and adaptable to changing priorities
- Knowledge of Quality Management Systems and LIMS
- Fluency in English; language skills in German
Aufgaben
- Review data from ELISA and qPCR analyses
- Check execution of assays in the lab
- Evaluate results for accuracy
- Assess quality parameters for stability studies
- Evaluate batch release quality
- Investigate unexpected results
- Ensure compliance with GMP and internal procedures
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Bachelor-AbschlussODER
- Master-Abschluss
Sprachen
- Englisch – fließend
- Deutsch – Grundkenntnisse
Tools & Technologien
- qPCR
- ELISA
- Quality Management Systems
- LIMS
Benefits
Boni & Prämien
- Compensation programs recognizing high performance
Mitarbeiterrabatte
- Numerous lifestyle benefits
- Leisure benefits
Familienfreundlichkeit
- Family benefits
Karriere- und Weiterentwicklung
- Agile career
Lockere Unternehmenskultur
- Dynamic work culture
- Inclusive workplace
Sinnstiftende Arbeit
- 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?
- Lonza
Senior Batch Record Reviewer(m/w/x)
Vollzeitnur vor OrtSeniorVisp - CH12 Lonza AG
QC Laborantin:in(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp - Lonza
QA Specialist, Batch Record Review(m/w/x)
Vollzeitnur vor OrtJuniorVisp - Lonza
QC Deviation & Investigation Specialist(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp - CH12 Lonza AG
Senior Labortechniker QC mit dem Schwerpunkt Bioanalytik(m/w/x)
Vollzeitnur vor OrtSeniorVisp