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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.
Requirements
- 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
Tasks
- 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
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Tools & Technologies
- GMP
Benefits
Bonuses & Incentives
- Performance-based compensation programs
Corporate Discounts
- Lifestyle benefits
- Leisure benefits
Family Support
- Family benefits
Career Advancement
- Agile career
Informal Culture
- Dynamic work culture
Purpose-Driven Work
- Inclusive and ethical workplace
Other Benefits
- Relocation assistance
Not a perfect match?
- LonzaFull-timeOn-siteSeniorVisp
- CH12 Lonza AG
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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.
Requirements
- 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
Tasks
- 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
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Tools & Technologies
- GMP
Benefits
Bonuses & Incentives
- Performance-based compensation programs
Corporate Discounts
- Lifestyle benefits
- Leisure benefits
Family Support
- Family benefits
Career Advancement
- Agile career
Informal Culture
- Dynamic work culture
Purpose-Driven Work
- Inclusive and ethical workplace
Other Benefits
- Relocation assistance
About the Company
CH12 Lonza AG
Industry
Pharmaceuticals
Description
The company is a global leader in life sciences, dedicated to improving lives through innovative solutions.
Not a perfect match?
- Lonza
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Associate Director CQV Integrated Biologics(m/w/x)
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Associate Director, QA SAP Project Management(m/w/x)
Full-timeOn-siteSeniorVisp - ten23 health
Head of Quality & GMP Operations(m/w/x)
Full-timeOn-siteSeniorVisp - CH12 Lonza AG
Senior QA Specialist(m/w/x)
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