CH12 Lonza AG
Associate Director CQV Integrated Biologics(m/w/x)
Full-timeOn-siteSenior
Visp
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LOLonza
Head of CQV/CSV - Advanced Synthesis Conjugates(m/w/x)
Visp
Full-timeOn-siteSenior
Nejo AI Summary
Defining validation strategy for complex synthesis facilities, providing technical expertise for equipment and clean rooms in biopharma. Leadership in validation within biopharma and strong cGMP background required. High performance compensation programs.
Requirements
- Leadership in CQV/CSV within biopharma
- Strong background in cGMPs
- Knowledge of engineering and manufacturing
- Leadership skills and team orientation
- Outstanding internal and external communication
- Structured and well-organized working attitude
- Agility, motivation, and success drive
- Proficiency in German and English
Tasks
- Lead and develop a specialized CQV and CSV team
- Hire and qualify team members
- Define the CQV and CSV strategy for synthesis facilities
- Provide technical expertise for equipment and clean rooms
- Bridge the gap between engineering and operations
- Make strategic decisions on validation standards
- Ensure compliance in commissioning and qualification phases
- Support GMP risk assessments
- Act as a subject matter expert during audits
- Contribute to the development of global CQV standards
- Manage resources and drive continuous process improvements
- Collaborate with manufacturing, QA, and engineering departments
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- CQV
- CSV
- cGMPs
Benefits
Bonuses & Incentives
- High performance compensation programs
Family Support
- Lifestyle, family, and leisure benefits
Career Advancement
- Agile career
Informal Culture
- Dynamic working culture
Purpose-Driven Work
- Inclusive and ethical workplace
Other Benefits
- Relocation assistance
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.
Not a perfect match?
- Lonza
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Full-timeOn-siteSeniorVisp - Lonza
Qualification CQV Engineer(m/w/x)
Full-timeOn-siteExperiencedVisp - CH12 Lonza AG
CSV Engineer(m/w/x)
Full-timeOn-siteSeniorVisp
LOLonza
Head of CQV/CSV - Advanced Synthesis Conjugates(m/w/x)
Visp
Full-timeOn-siteSenior
Nejo AI Summary
Defining validation strategy for complex synthesis facilities, providing technical expertise for equipment and clean rooms in biopharma. Leadership in validation within biopharma and strong cGMP background required. High performance compensation programs.
Requirements
- Leadership in CQV/CSV within biopharma
- Strong background in cGMPs
- Knowledge of engineering and manufacturing
- Leadership skills and team orientation
- Outstanding internal and external communication
- Structured and well-organized working attitude
- Agility, motivation, and success drive
- Proficiency in German and English
Tasks
- Lead and develop a specialized CQV and CSV team
- Hire and qualify team members
- Define the CQV and CSV strategy for synthesis facilities
- Provide technical expertise for equipment and clean rooms
- Bridge the gap between engineering and operations
- Make strategic decisions on validation standards
- Ensure compliance in commissioning and qualification phases
- Support GMP risk assessments
- Act as a subject matter expert during audits
- Contribute to the development of global CQV standards
- Manage resources and drive continuous process improvements
- Collaborate with manufacturing, QA, and engineering departments
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- CQV
- CSV
- cGMPs
Benefits
Bonuses & Incentives
- High performance compensation programs
Family Support
- Lifestyle, family, and leisure benefits
Career Advancement
- Agile career
Informal Culture
- Dynamic working culture
Purpose-Driven Work
- Inclusive and ethical workplace
Other Benefits
- Relocation assistance
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.
Not a perfect match?
- CH12 Lonza AG
Associate Director CQV Integrated Biologics(m/w/x)
Full-timeOn-siteSeniorVisp - Lonza
Team Lead CSV Biologics(m/w/x)
Full-timeOn-siteSeniorVisp - Lonza
Functional Lead QA CSV(m/w/x)
Full-timeOn-siteSeniorVisp - Lonza
Qualification CQV Engineer(m/w/x)
Full-timeOn-siteExperiencedVisp - CH12 Lonza AG
CSV Engineer(m/w/x)
Full-timeOn-siteSeniorVisp