Die KI-Suchmaschine für Jobs
QC Deviation & Investigation Specialist(m/w/x)
Beschreibung
You will ensure the safety of biologics manufacturing by leading investigations and managing compliance. Your day-to-day involves driving corrective actions and optimizing laboratory workflows.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
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
Ausbildung
Berufserfahrung
ca. 1 - 4 Jahre
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
Tools & Technologien
Sprachen
Englisch – verhandlungssicher
Deutsch – Grundkenntnisse
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
- CH12 Lonza AGVollzeitnur vor OrtJuniorVisp
- CH12 Lonza AG
Deviation Specialist(m/w/x)
Vollzeitnur vor OrtKeine AngabeVisp - Lonza
Senior Deviation Specialist(m/w/x)
Vollzeitnur vor OrtSeniorVisp - CH12 Lonza AG
Senior QA Specialist(m/w/x)
Vollzeitnur vor OrtSeniorVisp - Lonza
Senior QA Specialist/QA Project Manager(m/w/x)
Vollzeitnur vor OrtSeniorVisp
QC Deviation & Investigation Specialist(m/w/x)
Die KI-Suchmaschine für Jobs
Beschreibung
You will ensure the safety of biologics manufacturing by leading investigations and managing compliance. Your day-to-day involves driving corrective actions and optimizing laboratory workflows.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
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
Ausbildung
Berufserfahrung
ca. 1 - 4 Jahre
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
Tools & Technologien
Sprachen
Englisch – verhandlungssicher
Deutsch – Grundkenntnisse
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.
- CH12 Lonza AG
Investigation Specialist(m/w/x)
Vollzeitnur vor OrtJuniorVisp - CH12 Lonza AG
Deviation Specialist(m/w/x)
Vollzeitnur vor OrtKeine AngabeVisp - Lonza
Senior Deviation Specialist(m/w/x)
Vollzeitnur vor OrtSeniorVisp - CH12 Lonza AG
Senior QA Specialist(m/w/x)
Vollzeitnur vor OrtSeniorVisp - Lonza
Senior QA Specialist/QA Project Manager(m/w/x)
Vollzeitnur vor OrtSeniorVisp