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QC Deviation & Investigation Specialist(m/w/x)
Leading deviation management and document approval (DMS) in life sciences, executing tasks within LIMS. MSc or PhD in scientific/technical field required, QMS or TrackWise experience essential. High performance compensation programs, lifestyle and family benefits offered.
Anforderungen
- MSc or PhD in scientific or technical field
- Experience with Quality Management Systems or TrackWise
- GMP knowledge as an advantage
- Strong problem‑solving ability and proactive mindset
- Excellent analytical and technical understanding
- Business‑fluent English and German skills
Aufgaben
- Lead deviation management in your assigned area
- Drive corrective and preventive actions
- Create, review, and approve DMS documents
- Support continuous improvement for QC 24/7 processes
- Execute essential tasks within the LIMS system
- Implement operational changes to meet business needs
- Act as the primary contact for compliance topics
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
- Deutsch – Grundkenntnisse
Tools & Technologien
- TrackWise
- Quality Management Systems
- GMP
Benefits
Boni & Prämien
- High performance compensation programs
Familienfreundlichkeit
- Lifestyle, family, and leisure benefits
Karriere- und Weiterentwicklung
- Agile career
Lockere Unternehmenskultur
- Dynamic work culture
Sinnstiftende Arbeit
- Inclusive and ethical workplace
Sonstige Vorteile
- Relocation assistance
Noch nicht perfekt?
- CH12 Lonza AGVollzeitnur vor OrtKeine AngabeVisp
- CH12 Lonza AG
Investigation Specialist(m/w/x)
Vollzeitnur vor OrtJuniorVisp - CH12 Lonza AG
GMP Ops Support(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp - CH12 Lonza AG
Senior QA Specialist(m/w/x)
Vollzeitnur vor OrtSeniorVisp - Lonza
Senior Deviation Specialist(m/w/x)
Vollzeitnur vor OrtSeniorVisp
QC Deviation & Investigation Specialist(m/w/x)
Leading deviation management and document approval (DMS) in life sciences, executing tasks within LIMS. MSc or PhD in scientific/technical field required, QMS or TrackWise experience essential. High performance compensation programs, lifestyle and family benefits offered.
Anforderungen
- MSc or PhD in scientific or technical field
- Experience with Quality Management Systems or TrackWise
- GMP knowledge as an advantage
- Strong problem‑solving ability and proactive mindset
- Excellent analytical and technical understanding
- Business‑fluent English and German skills
Aufgaben
- Lead deviation management in your assigned area
- Drive corrective and preventive actions
- Create, review, and approve DMS documents
- Support continuous improvement for QC 24/7 processes
- Execute essential tasks within the LIMS system
- Implement operational changes to meet business needs
- Act as the primary contact for compliance topics
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
- Deutsch – Grundkenntnisse
Tools & Technologien
- TrackWise
- Quality Management Systems
- GMP
Benefits
Boni & Prämien
- High performance compensation programs
Familienfreundlichkeit
- Lifestyle, family, and leisure benefits
Karriere- und Weiterentwicklung
- Agile career
Lockere Unternehmenskultur
- Dynamic work 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
Deviation Specialist(m/w/x)
Vollzeitnur vor OrtKeine AngabeVisp - CH12 Lonza AG
Investigation Specialist(m/w/x)
Vollzeitnur vor OrtJuniorVisp - CH12 Lonza AG
GMP Ops Support(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp - CH12 Lonza AG
Senior QA Specialist(m/w/x)
Vollzeitnur vor OrtSeniorVisp - Lonza
Senior Deviation Specialist(m/w/x)
Vollzeitnur vor OrtSeniorVisp