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Senior QA Specialist, DPS (Drug Product Services)(m/w/x)
Dedicated shop floor QA oversight for manufacturing processes at a global life sciences contract manufacturer. Long-term pharmaceutical GMP environment experience required. Cross-functional team collaboration.
Anforderungen
- University degree in Chemistry, Biology, Biotechnology, or related field
- Long-term experience in pharmaceutical GMP environment
- Experience in QA department as an advantage
- Fluent English and advantageous German skills
Aufgaben
- Represent Quality Assurance in cross-functional teams
- Maintain interfaces with manufacturing and engineering teams
- Execute tasks related to drug product processes
- Act as the primary contact for manufacturing QA issues
- Provide dedicated shop floor QA oversight
- Approve quality records including deviations and CAPAs
- Review GMP-relevant documents and batch records
- Present QA topics during customer and regulatory audits
- Deliver GXP-related trainings to operations personnel
- Support product-specific and regulatory risk assessments
- Contribute to continuous improvement of the Quality Management System
Berufserfahrung
- ca. 4 - 6 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
- Deutsch – Grundkenntnisse
Tools & Technologien
- GMP
Benefits
Boni & Prämien
- Performance-based compensation programs
Karriere- und Weiterentwicklung
- Agile career
Lockere Unternehmenskultur
- Dynamic working culture
Sinnstiftende Arbeit
- Inclusive and ethical workplace
Noch nicht perfekt?
- CH12 Lonza AGVollzeitnur vor OrtSeniorVisp
- CH12 Lonza AG
Senior QA Specialist, QA Project Management(m/w/x)
Vollzeitnur vor OrtSeniorVisp - Lonza
Senior QA Specialist/QA Project Manager(m/w/x)
Vollzeitnur vor OrtSeniorVisp - Lonza
Senior QA Specialist - Product Quality Review(m/w/x)
Vollzeitnur vor OrtSeniorVisp - Lonza
Senior QA Specialist, QA Operations(m/w/x)
Vollzeitnur vor OrtSeniorVisp
Senior QA Specialist, DPS (Drug Product Services)(m/w/x)
Dedicated shop floor QA oversight for manufacturing processes at a global life sciences contract manufacturer. Long-term pharmaceutical GMP environment experience required. Cross-functional team collaboration.
Anforderungen
- University degree in Chemistry, Biology, Biotechnology, or related field
- Long-term experience in pharmaceutical GMP environment
- Experience in QA department as an advantage
- Fluent English and advantageous German skills
Aufgaben
- Represent Quality Assurance in cross-functional teams
- Maintain interfaces with manufacturing and engineering teams
- Execute tasks related to drug product processes
- Act as the primary contact for manufacturing QA issues
- Provide dedicated shop floor QA oversight
- Approve quality records including deviations and CAPAs
- Review GMP-relevant documents and batch records
- Present QA topics during customer and regulatory audits
- Deliver GXP-related trainings to operations personnel
- Support product-specific and regulatory risk assessments
- Contribute to continuous improvement of the Quality Management System
Berufserfahrung
- ca. 4 - 6 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
- Deutsch – Grundkenntnisse
Tools & Technologien
- GMP
Benefits
Boni & Prämien
- Performance-based compensation programs
Karriere- und Weiterentwicklung
- Agile career
Lockere Unternehmenskultur
- Dynamic working culture
Sinnstiftende Arbeit
- Inclusive and ethical workplace
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
Senior QA Specialist(m/w/x)
Vollzeitnur vor OrtSeniorVisp - CH12 Lonza AG
Senior QA Specialist, QA Project Management(m/w/x)
Vollzeitnur vor OrtSeniorVisp - Lonza
Senior QA Specialist/QA Project Manager(m/w/x)
Vollzeitnur vor OrtSeniorVisp - Lonza
Senior QA Specialist - Product Quality Review(m/w/x)
Vollzeitnur vor OrtSeniorVisp - Lonza
Senior QA Specialist, QA Operations(m/w/x)
Vollzeitnur vor OrtSeniorVisp