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Scientist, Process Development, Tech Ops(m/w/x)
Executing laboratory experiments for biotherapeutic process development, contributing to QbD activities. 2+ years industry experience in protein/biological process development required. Well-being support.
Requirements
- BS or MS in Biochemistry, Life Sciences, or related discipline required
- PhD or equivalent experience preferred
- 2+ years industry and managerial experience in pharmaceutical or biological operations
- Experience in protein/biological process development
- Cross-functional work ability
Tasks
- Execute laboratory experiments according to protocols and timelines
- Apply scientific methods to generate accurate and reliable data
- Contribute to Quality by Design (QbD) activities with experimental data
- Analyze and document experimental results and observations
- Prepare and maintain high-quality laboratory documentation
- Contribute to Life-Cycle Management (LCM) and Sustain & Improve activities
- Collaborate with project teams and laboratory groups
- Adhere to safety, quality, compliance, and regulatory requirements
Work Experience
- 2 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
Benefits
Mental Health Support
- Well-being support
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Scientist, Process Development, Tech Ops(m/w/x)
Executing laboratory experiments for biotherapeutic process development, contributing to QbD activities. 2+ years industry experience in protein/biological process development required. Well-being support.
Requirements
- BS or MS in Biochemistry, Life Sciences, or related discipline required
- PhD or equivalent experience preferred
- 2+ years industry and managerial experience in pharmaceutical or biological operations
- Experience in protein/biological process development
- Cross-functional work ability
Tasks
- Execute laboratory experiments according to protocols and timelines
- Apply scientific methods to generate accurate and reliable data
- Contribute to Quality by Design (QbD) activities with experimental data
- Analyze and document experimental results and observations
- Prepare and maintain high-quality laboratory documentation
- Contribute to Life-Cycle Management (LCM) and Sustain & Improve activities
- Collaborate with project teams and laboratory groups
- Adhere to safety, quality, compliance, and regulatory requirements
Work Experience
- 2 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
Benefits
Mental Health Support
- Well-being support
About the Company
CSL Behring
Industry
Pharmaceuticals
Description
Das Unternehmen ist ein globaler Marktführer in der Biotherapeutik, der innovative Therapien für Patienten mit immunologischen, hämatologischen, kardiovaskulären und anderen Erkrankungen entwickelt.
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