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Leading pharmaceutical development projects for biotech products, ensuring QC delivery and documentation. MSc/PhD in relevant science with cGMP analytics experience required. Performance-based compensation programs.
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 proactive attitude
- Detail-oriented and ability to work in matrix organization
- Business fluent English, written and spoken
Tasks
- Lead pharmaceutical development projects
- Ensure timely delivery of QC work-packages
- Ensure timely delivery of documentation
- Represent QC in internal meetings
- Represent QC in customer meetings
- Address risks proactively
- Communicate effectively
- Maintain compliance with cGMP
- Maintain compliance with SOPs
- Support audits
- Act as SME for QC topics
- Drive process improvements
- Share best practices
Work Experience
- approx. 1 - 4 years
Education
- Master's degree
Languages
- English – Business Fluent
Benefits
Bonuses & Incentives
- Compensation programs that recognize high performance
Not a perfect match?
- LonzaFull-timeOn-siteSeniorBasel
- Lonza
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Associate Principal Scientist Bioanalytics(m/w/x)
Full-timeOn-siteExperiencedBasel, Stein (AR)
Leading pharmaceutical development projects for biotech products, ensuring QC delivery and documentation. MSc/PhD in relevant science with cGMP analytics experience required. Performance-based compensation programs.
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 proactive attitude
- Detail-oriented and ability to work in matrix organization
- Business fluent English, written and spoken
Tasks
- Lead pharmaceutical development projects
- Ensure timely delivery of QC work-packages
- Ensure timely delivery of documentation
- Represent QC in internal meetings
- Represent QC in customer meetings
- Address risks proactively
- Communicate effectively
- Maintain compliance with cGMP
- Maintain compliance with SOPs
- Support audits
- Act as SME for QC topics
- Drive process improvements
- Share best practices
Work Experience
- approx. 1 - 4 years
Education
- Master's degree
Languages
- English – Business Fluent
Benefits
Bonuses & Incentives
- Compensation programs that recognize high performance
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.
Not a perfect match?
- Lonza
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Principal Scientist-Analytical Project Leader(m/w/x)
Full-timeOn-siteSeniorBasel - Roche
Group Head in Analytical Development & Quality Control(m/w/x)
Full-timeOn-siteManagementBasel - Novartis Pharma AG
Analytical Project Leader(m/w/x)
Full-timeOn-siteSeniorBasel - Lonza
Associate Principal Scientist Bioanalytics(m/w/x)
Full-timeOn-siteExperiencedBasel, Stein (AR)