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Project Lead Phys-Chem QC(m/w/x)
Description
In this role, you will lead pharmaceutical development projects, ensuring that quality control work is delivered on time while maintaining compliance. You will also represent QC in meetings, address risks, and drive process improvements to enhance operations.
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Requirements
- •MSc or PhD in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences or related field
- •Experience in Analytics or Quality Control under cGMP regulations
- •Knowledge of analytical lifecycle for biotechnology products and CMC requirements
- •Strong communication and interpersonal skills with a proactive attitude
- •Detail-oriented and able to work in a matrix organization
- •Business fluent English, written and spoken
Education
Work Experience
approx. 4 - 6 years
Tasks
- •Lead pharmaceutical development projects from early phases to market readiness
- •Ensure timely delivery of QC work-packages and documentation
- •Represent QC in internal and customer meetings
- •Proactively address risks and communicate effectively
- •Maintain compliance with cGMP and SOPs
- •Support audits and act as a subject matter expert for QC topics
- •Drive process improvements and share best practices
Languages
English – Business Fluent
Benefits
Bonuses & Incentives
- •Compensation programs that recognize high performance
Career Advancement
- •Agile career
Informal Culture
- •Dynamic work culture
Purpose-Driven Work
- •Inclusive and ethical workplace
- LonzaFull-timeOn-siteSeniorBasel
- Novartis Pharma AG
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Project Lead Phys-Chem QC(m/w/x)
The AI Job Search Engine
Description
In this role, you will lead pharmaceutical development projects, ensuring that quality control work is delivered on time while maintaining compliance. You will also represent QC in meetings, address risks, and drive process improvements to enhance operations.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •MSc or PhD in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences or related field
- •Experience in Analytics or Quality Control under cGMP regulations
- •Knowledge of analytical lifecycle for biotechnology products and CMC requirements
- •Strong communication and interpersonal skills with a proactive attitude
- •Detail-oriented and able to work in a matrix organization
- •Business fluent English, written and spoken
Education
Work Experience
approx. 4 - 6 years
Tasks
- •Lead pharmaceutical development projects from early phases to market readiness
- •Ensure timely delivery of QC work-packages and documentation
- •Represent QC in internal and customer meetings
- •Proactively address risks and communicate effectively
- •Maintain compliance with cGMP and SOPs
- •Support audits and act as a subject matter expert for QC topics
- •Drive process improvements and share best practices
Languages
English – Business Fluent
Benefits
Bonuses & Incentives
- •Compensation programs that recognize high performance
Career Advancement
- •Agile career
Informal Culture
- •Dynamic work culture
Purpose-Driven Work
- •Inclusive and ethical workplace
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.
- Lonza
Principal Scientist-Analytical Project Leader(m/w/x)
Full-timeOn-siteSeniorBasel - Novartis Pharma AG
Analytical Project Leader(m/w/x)
Full-timeOn-siteSeniorBasel - Roche
Group Head in Analytical Development & Quality Control(m/w/x)
Full-timeOn-siteManagementBasel - 1201 F. Hoffmann-La Roche AG
Group Head Particle Laboratory in Analytical Development and Quality Control(m/w/x)
Full-timeOn-siteSeniorBasel - CH12 Lonza AG
Senior Scientist Quality Control(m/w/x)
Full-timeOn-siteSeniorBasel, Stein (AR)