CH12 Lonza AG
Senior Scientist Quality Control(m/w/x)
Full-timeOn-siteSenior
Basel, Stein (AR)
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CHCH12 Lonza AG
Scientist Quality Control, physico-chemical analysis(m/w/x)
Stein (AR)
Full-timeOn-siteExperienced
Nejo AI Summary
Drug Product release and stability testing in cGMP lab, including mobile phase preparations and assay documentation. Experience with iCIEF, CE-SDS, and method validation in cGMP environment required. Relocation assistance available.
Requirements
- Solid work experience in cGMP controlled environment
- Experience with iCIEF, CE-SDS, and basic phys/chem techniques (e.g. pH, UV-VIS, osmolality, HPLC) and understanding of current requirements and documentation
- Experience with method validation and method transfer according to GMP
- Apprenticeship as Lab technician, Bachelor or equivalent in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences or related field
- Knowledge of lab quality systems like LIMS, Tiamo or CDS like Empower/Chromeleon
- Fluency in written and spoken English, German is an asset
- Ability to work independently and in a dynamic & fast-paced project environment, proactive attitude
Tasks
- Execute physico-chemical and biochemical Drug Product release testing
- Review stability testing under cGMP following existing method SOPs
- Document assay execution under cGMP and Good Documentation Practices
- Flag relevant observations to the supervisor for assessment
- Perform operational tasks in the lab, including mobile phase preparations
- Calibrate equipment and maintain adherence to 6S standards
- Manage consumables and support equipment maintenance
- Contribute to validation and transfer activities for new projects
- Assist in investigation and troubleshooting for assigned tasks
Work Experience
- approx. 1 - 4 years
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- English – Business Fluent
- German – Basic
Tools & Technologies
- iCIEF
- CE-SDS
- HPLC
- LIMS
- Tiamo
- Empower
- Chromeleon
Benefits
Bonuses & Incentives
- Compensation programs for high performance
Corporate Discounts
- Lifestyle benefits
- Leisure benefits
Family Support
- Family benefits
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.
Not a perfect match?
- CH12 Lonza AG
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CHCH12 Lonza AG
Scientist Quality Control, physico-chemical analysis(m/w/x)
Stein (AR)
Full-timeOn-siteExperienced
Nejo AI Summary
Drug Product release and stability testing in cGMP lab, including mobile phase preparations and assay documentation. Experience with iCIEF, CE-SDS, and method validation in cGMP environment required. Relocation assistance available.
Requirements
- Solid work experience in cGMP controlled environment
- Experience with iCIEF, CE-SDS, and basic phys/chem techniques (e.g. pH, UV-VIS, osmolality, HPLC) and understanding of current requirements and documentation
- Experience with method validation and method transfer according to GMP
- Apprenticeship as Lab technician, Bachelor or equivalent in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences or related field
- Knowledge of lab quality systems like LIMS, Tiamo or CDS like Empower/Chromeleon
- Fluency in written and spoken English, German is an asset
- Ability to work independently and in a dynamic & fast-paced project environment, proactive attitude
Tasks
- Execute physico-chemical and biochemical Drug Product release testing
- Review stability testing under cGMP following existing method SOPs
- Document assay execution under cGMP and Good Documentation Practices
- Flag relevant observations to the supervisor for assessment
- Perform operational tasks in the lab, including mobile phase preparations
- Calibrate equipment and maintain adherence to 6S standards
- Manage consumables and support equipment maintenance
- Contribute to validation and transfer activities for new projects
- Assist in investigation and troubleshooting for assigned tasks
Work Experience
- approx. 1 - 4 years
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- English – Business Fluent
- German – Basic
Tools & Technologies
- iCIEF
- CE-SDS
- HPLC
- LIMS
- Tiamo
- Empower
- Chromeleon
Benefits
Bonuses & Incentives
- Compensation programs for high performance
Corporate Discounts
- Lifestyle benefits
- Leisure benefits
Family Support
- Family benefits
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.
Not a perfect match?
- CH12 Lonza AG
Senior Scientist Quality Control(m/w/x)
Full-timeOn-siteSeniorBasel, Stein (AR) - CH12 Lonza AG
Scientist Microbiology, Quality Control(m/w/x)
Full-timeOn-siteExperiencedStein (AR) - Lonza
Senior Scientist, Equipment Qualification(m/w/x)
Full-timeOn-siteSeniorStein (AR) - Eurofins Scientific
Drug Substance Scientist / Manager (CMC – API)(m/w/x)
Full-timeOn-siteSeniorSankt Gallen - Lonza
Associate Principal Scientist Bioanalytics(m/w/x)
Full-timeOn-siteExperiencedBasel, Stein (AR)