Lonza
Junior Project Leader Quality Control for Drug Product(m/w/x)
Full-timeOn-siteJunior
Visp
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CHCH12 Lonza AG
Scientist Quality Control – Stability Studies(m/w/x)
Visp
Full-timeOn-siteJunior
Nejo AI Summary
Managing independent QC projects, interpreting complex data, and overseeing storage chambers for pharmaceutical development. Experience with IT quality systems (LIMS, TrackWise) required. Relocation assistance provided.
Requirements
- University degree in chemistry, biology, biochemistry, or related fields
- Ability to analyse large and complex data sets
- Team player and good communication skills
- Experience in pharmaceutical industry and/or GMP
- Experience with IT quality systems (e.g. LIMS, TrackWise)
- Fluency in English and understanding of German
Tasks
- Manage stability studies and projects independently
- Write and review protocols, reports, and SOPs for stability studies
- Interpret and present stability data
- Troubleshoot on a scientific basis
- Oversee storage chambers, including qualification and monitoring
- Identify and implement improvements and new technical solutions
- Handle deviations and out-of-specification results related to stability studies
Education
- Master's degree
Languages
- English – Business Fluent
- German – Basic
Tools & Technologies
- LIMS
- TrackWise
Benefits
Bonuses & Incentives
- Compensation programs for high performance
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 CH12 Lonza AG 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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CHCH12 Lonza AG
Scientist Quality Control – Stability Studies(m/w/x)
Visp
Full-timeOn-siteJunior
Nejo AI Summary
Managing independent QC projects, interpreting complex data, and overseeing storage chambers for pharmaceutical development. Experience with IT quality systems (LIMS, TrackWise) required. Relocation assistance provided.
Requirements
- University degree in chemistry, biology, biochemistry, or related fields
- Ability to analyse large and complex data sets
- Team player and good communication skills
- Experience in pharmaceutical industry and/or GMP
- Experience with IT quality systems (e.g. LIMS, TrackWise)
- Fluency in English and understanding of German
Tasks
- Manage stability studies and projects independently
- Write and review protocols, reports, and SOPs for stability studies
- Interpret and present stability data
- Troubleshoot on a scientific basis
- Oversee storage chambers, including qualification and monitoring
- Identify and implement improvements and new technical solutions
- Handle deviations and out-of-specification results related to stability studies
Education
- Master's degree
Languages
- English – Business Fluent
- German – Basic
Tools & Technologies
- LIMS
- TrackWise
Benefits
Bonuses & Incentives
- Compensation programs for high performance
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 CH12 Lonza AG 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
CH12 Lonza AG
Industry
Pharmaceuticals
Description
The company is a global leader in life sciences, dedicated to improving lives through innovative solutions.
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