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Scientist Quality Control – Stability Studies(m/w/x)
Description
In this role, you will independently manage stability studies while writing and reviewing essential documentation. Your day-to-day responsibilities will involve interpreting data, troubleshooting issues, and ensuring the integrity of storage chambers.
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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
Education
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
Tools & Technologies
Languages
English – Business Fluent
German – Basic
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
- CH12 Lonza AGFull-timeOn-siteExperiencedVisp
- Lonza
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Scientist Quality Control – Stability Studies(m/w/x)
The AI Job Search Engine
Description
In this role, you will independently manage stability studies while writing and reviewing essential documentation. Your day-to-day responsibilities will involve interpreting data, troubleshooting issues, and ensuring the integrity of storage chambers.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
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
Education
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
Tools & Technologies
Languages
English – Business Fluent
German – Basic
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
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.
- CH12 Lonza AG
Laborant(in) Stabilität(m/w/x)
Full-timeOn-siteExperiencedVisp - Lonza
(Senior) QA Operations Specialist, Small Molecules (Large Scale)(m/w/x)
Full-timeOn-siteJuniorVisp - CH12 Lonza AG
Laboratory Technician - HPLC - Quality Control for Biopharmaceuticals(m/w/x)
Full-timeOn-siteJuniorVisp - Lonza
QC Data Reviewer for Biochemical Methods(m/w/x)
Full-timeOn-siteExperiencedVisp - CH12 Lonza AG
Senior Labortechniker QC mit dem Schwerpunkt Bioanalytik(m/w/x)
Full-timeOn-siteSeniorVisp