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QA Operations Manager (Contamination Control)(m/w/x)
Description
You will safeguard product quality by leading contamination control strategies and providing expert QA guidance during audits to ensure microbial manufacturing remains compliant.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Degree in Life Sciences or related field
- •Experience in GMP-regulated environment, ideally biopharmaceutical
- •Proactive, detail-oriented, problem-solving and improvement mindset
- •Experience in customer-focused stakeholder management
- •Audit experience with Swissmedic/FDA/EMA regulations
- •Background in contamination control and monitoring
- •Fluency in English; German an asset
Education
Work Experience
approx. 4 - 6 years
Tasks
- •Lead asset-specific contamination prevention strategies
- •Ensure end-to-end compliance across microbial manufacturing
- •Author and approve critical GMP documentation
- •Review SOPs, deviations, and change controls
- •Conduct comprehensive quality risk assessments
- •Serve as primary QA expert during inspections
- •Manage microbial topics for customer and internal audits
- •Partner with cross-functional teams to identify risks
- •Drive deviation management and continuous improvement
- •Strengthen contamination prevention control practices
- •Provide microbiology and QA expertise to stakeholders
- •Foster a robust quality culture and operational compliance
Tools & Technologies
Languages
English – Business Fluent
German – Basic
Benefits
Career Advancement
- •Agile career
Informal Culture
- •Dynamic working culture
Purpose-Driven Work
- •Inclusive and ethical workplace
Bonuses & Incentives
- •Performance-based compensation programs
- CH12 Lonza AGFull-timeOn-siteSeniorVisp
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QA Operations Manager (Contamination Control)(m/w/x)
The AI Job Search Engine
Description
You will safeguard product quality by leading contamination control strategies and providing expert QA guidance during audits to ensure microbial manufacturing remains compliant.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Degree in Life Sciences or related field
- •Experience in GMP-regulated environment, ideally biopharmaceutical
- •Proactive, detail-oriented, problem-solving and improvement mindset
- •Experience in customer-focused stakeholder management
- •Audit experience with Swissmedic/FDA/EMA regulations
- •Background in contamination control and monitoring
- •Fluency in English; German an asset
Education
Work Experience
approx. 4 - 6 years
Tasks
- •Lead asset-specific contamination prevention strategies
- •Ensure end-to-end compliance across microbial manufacturing
- •Author and approve critical GMP documentation
- •Review SOPs, deviations, and change controls
- •Conduct comprehensive quality risk assessments
- •Serve as primary QA expert during inspections
- •Manage microbial topics for customer and internal audits
- •Partner with cross-functional teams to identify risks
- •Drive deviation management and continuous improvement
- •Strengthen contamination prevention control practices
- •Provide microbiology and QA expertise to stakeholders
- •Foster a robust quality culture and operational compliance
Tools & Technologies
Languages
English – Business Fluent
German – Basic
Benefits
Career Advancement
- •Agile career
Informal Culture
- •Dynamic working culture
Purpose-Driven Work
- •Inclusive and ethical workplace
Bonuses & Incentives
- •Performance-based compensation programs
About the Company
Lonza
Industry
Pharmaceuticals
Description
Lonza is a global leader in life sciences, committed to improving lives through innovative solutions and ethical practices.
- CH12 Lonza AG
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Full-timeOn-siteSeniorVisp - ten23 health
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Senior QA Specialist/QA Project Manager(m/w/x)
Full-timeOn-siteSeniorVisp