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QC Investigator(m/w/x)
Leading critical quality deviations and root cause analysis for pharmaceutical manufacturing at global pharma with 100,000+ employees. Extensive cGMP expertise and 3+ years pharma industry experience required. Exposure to global quality standards and regulations.
Anforderungen
- Degree in Life Sciences
- 3+ years of professional experience in pharmaceutical industry
- Experience in Quality Assurance or QC testing
- Extensive expertise in cGMP
- Knowledge of local and international GMP regulations
- Proficiency in LPS methodology
- Knowledge of root cause analysis
- Analytical ability to evaluate complex issues
- Results-oriented decision making
- Excellent communication skills in German or English
- Collaboration skills across global network
Aufgaben
- Lead critical and complex deviations and investigations
- Focus on quality KPIs to maintain high standards
- Support and guide deviation huddles for the QC organization
- Contribute to root cause analysis and implement CAPA measures
- Oversee improvement activities in deviations and investigations
- Enhance technical writing standards within the QC organization
- Collaborate with teams to ensure safety and reliability in analytical processes
Berufserfahrung
- 3 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Deutsch – verhandlungssicher
- Englisch – verhandlungssicher
Noch nicht perfekt?
- F. Hoffmann-La Roche AGVollzeitnur vor OrtSeniorKaiseraugst
- Novartis Pharma Schweizerhalle AG
QC Analyst II(m/w/x)
Vollzeitnur vor OrtBerufserfahrenBasel - Novartis Pharma Schweizerhalle AG
QC Analyst II(m/w/x)
Vollzeitnur vor OrtBerufserfahrenBasel - Novartis Pharma Stein AG
QC Analyst II(m/w/x)
VollzeitBefristeter Vertragnur vor OrtBerufserfahrenStein - Novartis Pharma Stein AG
QC Analyst II(m/w/x)
VollzeitBefristeter Vertragnur vor OrtBerufserfahrenStein
QC Investigator(m/w/x)
Leading critical quality deviations and root cause analysis for pharmaceutical manufacturing at global pharma with 100,000+ employees. Extensive cGMP expertise and 3+ years pharma industry experience required. Exposure to global quality standards and regulations.
Anforderungen
- Degree in Life Sciences
- 3+ years of professional experience in pharmaceutical industry
- Experience in Quality Assurance or QC testing
- Extensive expertise in cGMP
- Knowledge of local and international GMP regulations
- Proficiency in LPS methodology
- Knowledge of root cause analysis
- Analytical ability to evaluate complex issues
- Results-oriented decision making
- Excellent communication skills in German or English
- Collaboration skills across global network
Aufgaben
- Lead critical and complex deviations and investigations
- Focus on quality KPIs to maintain high standards
- Support and guide deviation huddles for the QC organization
- Contribute to root cause analysis and implement CAPA measures
- Oversee improvement activities in deviations and investigations
- Enhance technical writing standards within the QC organization
- Collaborate with teams to ensure safety and reliability in analytical processes
Berufserfahrung
- 3 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Deutsch – verhandlungssicher
- Englisch – verhandlungssicher
Über das Unternehmen
1201 F. Hoffmann-La Roche AG
Branche
Pharmaceuticals
Beschreibung
Roche is dedicated to advancing science and ensuring access to healthcare for everyone, with over 100,000 employees globally.
Noch nicht perfekt?
- F. Hoffmann-La Roche AG
Complaint Lead Investigator(m/w/x)
Vollzeitnur vor OrtSeniorKaiseraugst - Novartis Pharma Schweizerhalle AG
QC Analyst II(m/w/x)
Vollzeitnur vor OrtBerufserfahrenBasel - Novartis Pharma Schweizerhalle AG
QC Analyst II(m/w/x)
Vollzeitnur vor OrtBerufserfahrenBasel - Novartis Pharma Stein AG
QC Analyst II(m/w/x)
VollzeitBefristeter Vertragnur vor OrtBerufserfahrenStein - Novartis Pharma Stein AG
QC Analyst II(m/w/x)
VollzeitBefristeter Vertragnur vor OrtBerufserfahrenStein