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Key Expert Downstream Processing(m/w/x)
Optimizing downstream bioprocesses for biotechnological manufacturing, including chromatography, filtration, and drying. Hands-on cGMP and DoE experience required. Employee benefit programs.
Requirements
- PhD or Master's degree in Biology, Biotechnology, Biochemistry, Bioprocess Engineering, Chemical Engineering, Chemistry, or related field
- Hands-on laboratory experience in downstream processing including chromatography, crystallization, filtration, and drying processes
- Experience with cGMP environments
- Experience with Design of Experiments (DoE)
- Experience with process modeling
- Experience with preparative/analytical chromatography
- Proficiency in HPLC
- Proficiency in gel electrophoresis
- Proficiency in broad analytical methods
- Knowledge of enzyme kinetics advantageous
- Knowledge of protein folding advantageous
- Strong project management skills
- Ability to work across cultures
- Ability to bridge technical, manufacturing, quality, and regulatory requirements
- Fluency in English (verbal and written)
- Fluency in German (verbal and written)
- Chinese language skills advantageous
- Willingness to travel to China
- Willingness to support cross-cultural collaboration
- Willingness to support on-site implementation activities
Tasks
- Develop and optimize downstream bioprocesses
- Transfer bioprocesses for biotechnological manufacturing
- Implement chromatography, crystallization, precipitation, filtration, and drying
- Support scale-up activities and process characterization
- Troubleshoot and start up manufacturing operations
- Lead technology transfer between manufacturing sites
- Prepare process transfer documentation
- Develop regulatory submission documents
- Support process validations globally
- Establish laboratory infrastructure for process development
- Equip laboratory with necessary capabilities
- Provide technical input to regulatory dossiers
- Respond to authority questions on downstream processing
- Represent downstream processing in audits and inspections
Work Experience
- approx. 1 - 4 years
Education
- Master's degree
Languages
- English – Business Fluent
- German – Business Fluent
- Chinese – Basic
Tools & Technologies
- HPLC
- gel electrophoresis
Benefits
Corporate Discounts
- Employee benefit programs
Not a perfect match?
- Sanofi-Aventis Deutschland GmbHFull-timeOn-siteSeniorFrankfurt am Main
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Key Expert Downstream Processing(m/w/x)
Optimizing downstream bioprocesses for biotechnological manufacturing, including chromatography, filtration, and drying. Hands-on cGMP and DoE experience required. Employee benefit programs.
Requirements
- PhD or Master's degree in Biology, Biotechnology, Biochemistry, Bioprocess Engineering, Chemical Engineering, Chemistry, or related field
- Hands-on laboratory experience in downstream processing including chromatography, crystallization, filtration, and drying processes
- Experience with cGMP environments
- Experience with Design of Experiments (DoE)
- Experience with process modeling
- Experience with preparative/analytical chromatography
- Proficiency in HPLC
- Proficiency in gel electrophoresis
- Proficiency in broad analytical methods
- Knowledge of enzyme kinetics advantageous
- Knowledge of protein folding advantageous
- Strong project management skills
- Ability to work across cultures
- Ability to bridge technical, manufacturing, quality, and regulatory requirements
- Fluency in English (verbal and written)
- Fluency in German (verbal and written)
- Chinese language skills advantageous
- Willingness to travel to China
- Willingness to support cross-cultural collaboration
- Willingness to support on-site implementation activities
Tasks
- Develop and optimize downstream bioprocesses
- Transfer bioprocesses for biotechnological manufacturing
- Implement chromatography, crystallization, precipitation, filtration, and drying
- Support scale-up activities and process characterization
- Troubleshoot and start up manufacturing operations
- Lead technology transfer between manufacturing sites
- Prepare process transfer documentation
- Develop regulatory submission documents
- Support process validations globally
- Establish laboratory infrastructure for process development
- Equip laboratory with necessary capabilities
- Provide technical input to regulatory dossiers
- Respond to authority questions on downstream processing
- Represent downstream processing in audits and inspections
Work Experience
- approx. 1 - 4 years
Education
- Master's degree
Languages
- English – Business Fluent
- German – Business Fluent
- Chinese – Basic
Tools & Technologies
- HPLC
- gel electrophoresis
Benefits
Corporate Discounts
- Employee benefit programs
About the Company
Sanofi-Aventis Deutschland GmbH
Industry
Pharmaceuticals
Description
Das Unternehmen bietet Arzneimittel zur Prävention von Herz-Kreislauf-Erkrankungen an und setzt sich für die Verbesserung der Lebensqualität ein.
Not a perfect match?
- Sanofi-Aventis Deutschland GmbH
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Key Expert Process Analytical Technologies / Analytical Transfers(m/w/x)
Full-timeOn-siteExperiencedFrankfurt am Mainfrom 83,856 - 125,784 / year - Formo Foods GmbH
Research Associate - Downstream Processing(m/w/x)
Full-timeOn-siteExperiencedFrankfurt am Main - Sanofi-Aventis Deutschland GmbH
DSP Technician(m/w/x)
Full-timeTemporary contractOn-siteSeniorFrankfurt am Main - Sanofi-Aventis Deutschland GmbH
Laboratory Head Upstream Process Development(m/w/x)
Full-timeOn-siteExperiencedFrankfurt am Main