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Reviewing and approving GMP documentation and material releases in biopharmaceutical manufacturing. Solid QA experience in GMP, with material management background, required. Relocation assistance provided.
Requirements
- Solid QA experience in GMP environment
- Experience in material management or raw materials
- Scientific or technical education background
- Fluency in English and German skills
- Accurate and efficient work in regulated environment
- Collaborative and proactive cross-functional approach
Tasks
- Review and approve GMP documentation
- Approve methods, protocols, and specifications
- Oversee material testing and batch releases
- Investigate deviations and OOS/OOE results
- Manage change control and quality agreements
- Drive qualification and validation activities
- Maintain material master data in SAP
- Support warehouse and logistics quality oversight
- Participate in audits and inspections
- Lead cross-functional quality projects
- Train and mentor team members
- Deputize for the Team Lead as needed
- Shape new QMS platforms and systems
Education
- Vocational certification
Languages
- English – Business Fluent
- German – Basic
Tools & Technologies
- GMP
- CAPA
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
Informal Culture
- Dynamic work culture
Purpose-Driven Work
- Inclusive and ethical workplace
Not a perfect match?
- LonzaFull-timeOn-siteSeniorStein (AR)
- Lonza
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Reviewing and approving GMP documentation and material releases in biopharmaceutical manufacturing. Solid QA experience in GMP, with material management background, required. Relocation assistance provided.
Requirements
- Solid QA experience in GMP environment
- Experience in material management or raw materials
- Scientific or technical education background
- Fluency in English and German skills
- Accurate and efficient work in regulated environment
- Collaborative and proactive cross-functional approach
Tasks
- Review and approve GMP documentation
- Approve methods, protocols, and specifications
- Oversee material testing and batch releases
- Investigate deviations and OOS/OOE results
- Manage change control and quality agreements
- Drive qualification and validation activities
- Maintain material master data in SAP
- Support warehouse and logistics quality oversight
- Participate in audits and inspections
- Lead cross-functional quality projects
- Train and mentor team members
- Deputize for the Team Lead as needed
- Shape new QMS platforms and systems
Education
- Vocational certification
Languages
- English – Business Fluent
- German – Basic
Tools & Technologies
- GMP
- CAPA
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
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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