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Leading physical-chemical analytical work-packages for pharmaceutical development projects from early phases to market readiness at a global life sciences firm. MSc/PhD in Analytical Chemistry or related field, with cGMP analytical experience required. Cross-functional matrix organization, customer-facing role.
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
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
Work Experience
- approx. 4 - 6 years
Education
- Master's degree
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
Not a perfect match?
- LonzaFull-timeOn-siteManagementBasel
- Lonza
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Senior Laboratory Scientist Phys-Chemical QC(m/w/x)
Full-timeOn-siteSeniorBasel
Leading physical-chemical analytical work-packages for pharmaceutical development projects from early phases to market readiness at a global life sciences firm. MSc/PhD in Analytical Chemistry or related field, with cGMP analytical experience required. Cross-functional matrix organization, customer-facing role.
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
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
Work Experience
- approx. 4 - 6 years
Education
- Master's degree
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.
Not a perfect match?
- Lonza
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Principal Scientist-Analytical Project Leader(m/w/x)
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