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Associate Director, Quality Strategy and Operations(m/w/x)
Managing quality strategy and project portfolio for life sciences manufacturing operations. Stakeholder influence and cross-functional management essential. Performance-based compensation programs.
Anforderungen
- Degree in Life Sciences, Engineering, or Business
- Strong problem-solving and root cause analysis
- Fluent English (verbal and written)
- Drive to enhance team performance
- Stakeholder influence and cross-functional management
- Task prioritization in GMP-regulated environments
- Proactive escalation of compliance concerns
- Continuous improvement mindset
- Presentation skills for senior stakeholders
Aufgaben
- Lead and execute quality improvement initiatives
- Manage the site's quality project portfolio
- Design and maintain the quality organization's meeting structure
- Own agendas and follow-ups for strategic meetings
- Partner with manufacturing operations to align quality objectives
- Track and report on people, finance, and innovation initiatives
- Harmonize quality practices across site assets and technologies
- Support the Head of Quality in executing the Site Quality Plan
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- GMP
Benefits
Boni & Prämien
- Performance-based compensation programs
Mitarbeiterrabatte
- Lifestyle benefits
- Leisure benefits
Familienfreundlichkeit
- Family benefits
Karriere- und Weiterentwicklung
- Agile career
Lockere Unternehmenskultur
- Dynamic work culture
Sinnstiftende Arbeit
- Inclusive and ethical workplace
Sonstige Vorteile
- Relocation assistance
Noch nicht perfekt?
- LonzaVollzeitnur vor OrtSeniorVisp
- CH12 Lonza AG
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Head of Quality & GMP Operations(m/w/x)
Vollzeitnur vor OrtSeniorVisp - CH12 Lonza AG
Senior QA Specialist(m/w/x)
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Associate Director, Quality Strategy and Operations(m/w/x)
Managing quality strategy and project portfolio for life sciences manufacturing operations. Stakeholder influence and cross-functional management essential. Performance-based compensation programs.
Anforderungen
- Degree in Life Sciences, Engineering, or Business
- Strong problem-solving and root cause analysis
- Fluent English (verbal and written)
- Drive to enhance team performance
- Stakeholder influence and cross-functional management
- Task prioritization in GMP-regulated environments
- Proactive escalation of compliance concerns
- Continuous improvement mindset
- Presentation skills for senior stakeholders
Aufgaben
- Lead and execute quality improvement initiatives
- Manage the site's quality project portfolio
- Design and maintain the quality organization's meeting structure
- Own agendas and follow-ups for strategic meetings
- Partner with manufacturing operations to align quality objectives
- Track and report on people, finance, and innovation initiatives
- Harmonize quality practices across site assets and technologies
- Support the Head of Quality in executing the Site Quality Plan
Berufserfahrung
- ca. 1 - 4 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- GMP
Benefits
Boni & Prämien
- Performance-based compensation programs
Mitarbeiterrabatte
- Lifestyle benefits
- Leisure benefits
Familienfreundlichkeit
- Family benefits
Karriere- und Weiterentwicklung
- Agile career
Lockere Unternehmenskultur
- Dynamic work culture
Sinnstiftende Arbeit
- Inclusive and ethical workplace
Sonstige Vorteile
- Relocation assistance
Über das Unternehmen
CH12 Lonza AG
Branche
Pharmaceuticals
Beschreibung
The company is a global leader in life sciences, dedicated to improving lives through innovative solutions.
Noch nicht perfekt?
- Lonza
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Associate Director, QA SAP Project Management(m/w/x)
Vollzeitnur vor OrtSeniorVisp - ten23 health
Head of Quality & GMP Operations(m/w/x)
Vollzeitnur vor OrtSeniorVisp - CH12 Lonza AG
Senior QA Specialist(m/w/x)
Vollzeitnur vor OrtSeniorVisp