CH12 Lonza AG
Associate Director CQV Integrated Biologics(m/w/x)
Full-timeOn-siteSenior
Visp
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Commissioning and qualification of new biologics manufacturing equipment for global pharma. University degree and regulated environment experience required. Relocation assistance, agile career path.
Requirements
- University degree in Engineering, Life Sciences, or related field
- Professional experience in regulated environment (commissioning, qualification, validation)
- Independent and flexible work with strong communication skills
- Structured, focused, and organized working style
- Openness to new ideas, agility, proactive mindset
- Experience with COMOS, DMS, TrackWise, SAP is advantageous
- Business-fluent English required; German skills advantageous
Tasks
- Lead the CQV team functionally and disciplinarily
- Prepare commissioning and qualification documentation for new equipment
- Support modification, expansion, and new-build projects
- Perform PQs for critical systems in new-build projects
- Oversee all systems after release to production
- Manage deviations, GMP-related changes, and CAPAs
- Coordinate internal teams, external service providers, and suppliers
- Present qualification documentation during audits and inspections
- Qualify and validate process equipment and technical facilities
- Continuously optimize processes, systems, and internal workflows
- Ensure operations and engineering teams maintain technical expertise
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Basic
Tools & Technologies
- COMOS
- DMS
- TrackWise
- SAP
Benefits
Competitive Pay
- High-performance compensation programs
Other Benefits
- Relocation assistance
Career Advancement
- Agile career
Informal Culture
- Dynamic working culture
Purpose-Driven Work
- Inclusive and ethical workplace
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Lonza and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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Commissioning and qualification of new biologics manufacturing equipment for global pharma. University degree and regulated environment experience required. Relocation assistance, agile career path.
Requirements
- University degree in Engineering, Life Sciences, or related field
- Professional experience in regulated environment (commissioning, qualification, validation)
- Independent and flexible work with strong communication skills
- Structured, focused, and organized working style
- Openness to new ideas, agility, proactive mindset
- Experience with COMOS, DMS, TrackWise, SAP is advantageous
- Business-fluent English required; German skills advantageous
Tasks
- Lead the CQV team functionally and disciplinarily
- Prepare commissioning and qualification documentation for new equipment
- Support modification, expansion, and new-build projects
- Perform PQs for critical systems in new-build projects
- Oversee all systems after release to production
- Manage deviations, GMP-related changes, and CAPAs
- Coordinate internal teams, external service providers, and suppliers
- Present qualification documentation during audits and inspections
- Qualify and validate process equipment and technical facilities
- Continuously optimize processes, systems, and internal workflows
- Ensure operations and engineering teams maintain technical expertise
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Basic
Tools & Technologies
- COMOS
- DMS
- TrackWise
- SAP
Benefits
Competitive Pay
- High-performance compensation programs
Other Benefits
- Relocation assistance
Career Advancement
- Agile career
Informal Culture
- Dynamic working culture
Purpose-Driven Work
- Inclusive and ethical workplace
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Lonza and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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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- CH12 Lonza AG
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