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Scientist Commercial QC(m/w/x)
Description
You will ensure the quality of drug products by performing precise analytical testing and maintaining a high-standard lab environment while driving technical investigations and documentation.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Training as lab technician or BSc in Analytical Chemistry, Biochemistry or related field
- •Experience in GMP-regulated QC laboratory
- •Experience with HPLC, CE-SDS, icIEF, or ELISA (plus)
- •Understanding of cGMP, GDocP, and Data Integrity principles
- •Excellent communication skills in English
Education
Work Experience
approx. 1 - 4 years
Tasks
- •Perform analytical testing for drug products
- •Conduct batch release and stability studies
- •Execute and review basic laboratory tasks
- •Calibrate pH meters and check balances
- •Document assay performance following GDocP standards
- •Report relevant observations to your supervisor
- •Follow all applicable EHS regulations
- •Maintain laboratory cleanliness and audit readiness
- •Adhere to 6S and cGMP principles
- •Troubleshoot method and equipment issues
- •Propose mitigation measures for investigations
- •Draft method SOPs and technical reports
Tools & Technologies
Languages
English – Business Fluent
Benefits
Career Advancement
- •Agile career
Informal Culture
- •Dynamic work culture
Purpose-Driven Work
- •Inclusive and ethical workplace
Bonuses & Incentives
- •Performance-based compensation programs
- CH12 Lonza AGFull-timeOn-siteSeniorBasel, Stein (AR)
- Lonza
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Scientist Commercial QC(m/w/x)
The AI Job Search Engine
Description
You will ensure the quality of drug products by performing precise analytical testing and maintaining a high-standard lab environment while driving technical investigations and documentation.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Training as lab technician or BSc in Analytical Chemistry, Biochemistry or related field
- •Experience in GMP-regulated QC laboratory
- •Experience with HPLC, CE-SDS, icIEF, or ELISA (plus)
- •Understanding of cGMP, GDocP, and Data Integrity principles
- •Excellent communication skills in English
Education
Work Experience
approx. 1 - 4 years
Tasks
- •Perform analytical testing for drug products
- •Conduct batch release and stability studies
- •Execute and review basic laboratory tasks
- •Calibrate pH meters and check balances
- •Document assay performance following GDocP standards
- •Report relevant observations to your supervisor
- •Follow all applicable EHS regulations
- •Maintain laboratory cleanliness and audit readiness
- •Adhere to 6S and cGMP principles
- •Troubleshoot method and equipment issues
- •Propose mitigation measures for investigations
- •Draft method SOPs and technical reports
Tools & Technologies
Languages
English – Business Fluent
Benefits
Career Advancement
- •Agile career
Informal Culture
- •Dynamic work culture
Purpose-Driven Work
- •Inclusive and ethical workplace
Bonuses & Incentives
- •Performance-based compensation programs
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.
- CH12 Lonza AG
Senior Scientist Quality Control(m/w/x)
Full-timeOn-siteSeniorBasel, Stein (AR) - Lonza
Laboratory Scientist Phys-Chemical QC(m/w/x)
Full-timeOn-siteExperiencedBasel - Lonza
Laboratory Scientist Bioanalytics(m/w/x)
Full-timeOn-siteExperiencedBasel - CH12 Lonza AG
Senior GMP Validation Scientist – Laboratory Execution Physico-Chemical Quality Control(m/w/x)
Full-timeOn-siteSeniorBasel - Lonza
Scientist Primary Packaging and Raw Materials(m/w/x)
Full-timeOn-siteExperiencedBasel