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Compliance Engineer DPS Growth Project(m/w/x)
Description
You will ensure high-level GMP compliance at a sterile manufacturing site by managing documentation, leading CAPA lifecycles, and preparing the team for critical regulatory inspections.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Degree in Pharmacy, Engineering, or related field
- •Experience in pharmaceutical GMP and engineering
- •Solid project management skills
- •Excellent communication and detail-oriented working style
- •Knowledge of GMP and regulatory expectations
- •Fluency in German and English
- •Stakeholder collaboration and confident GMP representation
Education
Work Experience
approx. 1 - 4 years
Tasks
- •Create and review GMP documentation
- •Draft periodic reviews and qualification documents
- •Develop and update SOPs
- •Prepare presentation materials for audits
- •Organize subject matter experts for inspections
- •Coordinate with internal inspection teams
- •Support site-wide inspection readiness
- •Oversee GMP activities within CAPA processes
- •Manage change management workflows
- •Lead the full CAPA lifecycle
- •Execute and document re-qualification activities
- •Represent the Engineering Lead Team
Tools & Technologies
Languages
German – Business Fluent
English – Business Fluent
Benefits
Bonuses & Incentives
- •Performance-based compensation programs
Corporate Discounts
- •Lifestyle benefits
- •Leisure benefits
Family Support
- •Family benefits
Other Benefits
- •Relocation assistance
Career Advancement
- •Agile career opportunities
Informal Culture
- •Dynamic work culture
Purpose-Driven Work
- •Inclusive and ethical workplace
- LonzaFull-timeOn-siteExperiencedStein (AR)
- Lonza
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Senior QA Expert(m/w/x)
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Head Manufacturing for Lyophilized Vials in a Growth Project(m/w/x)
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Compliance Engineer DPS Growth Project(m/w/x)
The AI Job Search Engine
Description
You will ensure high-level GMP compliance at a sterile manufacturing site by managing documentation, leading CAPA lifecycles, and preparing the team for critical regulatory inspections.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Degree in Pharmacy, Engineering, or related field
- •Experience in pharmaceutical GMP and engineering
- •Solid project management skills
- •Excellent communication and detail-oriented working style
- •Knowledge of GMP and regulatory expectations
- •Fluency in German and English
- •Stakeholder collaboration and confident GMP representation
Education
Work Experience
approx. 1 - 4 years
Tasks
- •Create and review GMP documentation
- •Draft periodic reviews and qualification documents
- •Develop and update SOPs
- •Prepare presentation materials for audits
- •Organize subject matter experts for inspections
- •Coordinate with internal inspection teams
- •Support site-wide inspection readiness
- •Oversee GMP activities within CAPA processes
- •Manage change management workflows
- •Lead the full CAPA lifecycle
- •Execute and document re-qualification activities
- •Represent the Engineering Lead Team
Tools & Technologies
Languages
German – Business Fluent
English – Business Fluent
Benefits
Bonuses & Incentives
- •Performance-based compensation programs
Corporate Discounts
- •Lifestyle benefits
- •Leisure benefits
Family Support
- •Family benefits
Other Benefits
- •Relocation assistance
Career Advancement
- •Agile career opportunities
Informal Culture
- •Dynamic work culture
Purpose-Driven Work
- •Inclusive and ethical workplace
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.
- Lonza
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