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Compliance Engineer DPS Growth Project(m/w/x)
GMP documentation, SOPs, and audit material preparation for pharmaceutical manufacturing. Pharmaceutical GMP and engineering experience, plus project management skills, required. Relocation assistance provided.
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
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
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- GMP
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
Not a perfect match?
- LonzaFull-timeOn-siteExperiencedStein (AR)
- Lonza
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Senior QA Expert(m/w/x)
Full-timeOn-siteSeniorStein (AR)
Compliance Engineer DPS Growth Project(m/w/x)
GMP documentation, SOPs, and audit material preparation for pharmaceutical manufacturing. Pharmaceutical GMP and engineering experience, plus project management skills, required. Relocation assistance provided.
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
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
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- GMP
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.
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Full-timeOn-siteSeniorStein (AR)