Sanofi-Aventis Deutschland GmbH
Laboratory Head non-GMP PP Tech Area(m/w/x)
Vollzeitnur vor OrtSenior
Frankfurt am Main
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SASanofi-Aventis Deutschland GmbH
Scientist - Tech Area(m/w/x)
Frankfurt am Main
VollzeitVor OrtSenior
AI/ML
Nejo KI-Zusammenfassung
Scaling microbial projects for non-GMP drug substance production, implementing new continuous process technologies and AI solutions at a cardiovascular medicine developer. Experience in production (USP) and purification (DSP) of biologics with microbial systems required; mammalian cell culture experience beneficial. 14-week paid family leave, childcare benefits.
Anforderungen
- Advanced university degree (PhD/similar) in Natural Sciences/Engineering (Biology, Biotechnology, Chemical Engineering, or similar), or minimum 5 years professional experience
- Experience in production (USP) and purification (DSP) of biologics (microbial systems)
- Beneficial experience with mammalian cell culture
- Experience in scale-up and continuous production processes
- Experience in identification, evaluation, implementation of new technologies
- Experience in international/interdisciplinary project management
- Strong teamwork and communication skills
- Excellent organizational skills
- Collaborative spirit for cross-functional exchange
- Independent work style and solution-oriented approach
- High self-motivation, reliability, and responsibility
- Pioneering spirit and willingness to learn
- Knowledge/experience with biological product production processes (proteins, plasmids)
- Process engineering understanding; cultivation/purification scale-up knowledge
- Knowledge of continuous production processes
- Knowledge in bioanalytics
- Knowledge in process digitalization
- Beneficial programming skills, data analysis tools, multivariate data analysis know-how
- Analytical thinking and approach
- Very good IT skills (MS Office), knowledge of IT-supported plant systems
Aufgaben
- Support non-GMP production (USP) of microbial drug substance.
- Support non-GMP purification (DSP) of microbial drug substance.
- Identify and evaluate new technical scale technologies.
- Implement new technical scale technologies.
- Pioneer continuous and disposable production processes.
- Assess feasibility of GMP facilities.
- Evaluate GMP facility robustness and performance.
- Select or design new production facilities.
- Plan microbial projects at non-GMP technical scale.
- Scale up microbial projects at non-GMP technical scale.
- Supply technical material for microbial projects.
- Analyze technical material for microbial projects.
- Troubleshoot microbial projects at non-GMP technical scale.
- Characterize and evaluate equipment.
- Develop predictive models for continuous processes.
- Develop predictive models for process scalability.
- Introduce electronic systems and AI solutions.
- Digitalize processes, workflows, and documentation.
- Digitalize analysis of process-relevant production data.
- Organize and coordinate lab and process procedures.
- Optimize lab and process procedures.
- Ensure compliance with guidelines and safety regulations.
- Establish protocols and safety evaluations.
- Establish working procedures.
- Plan and execute experiments.
- Develop and document experiments.
- Incorporate in-process analytical methods.
- Ensure efficient and documented process transfer.
- Transfer processes to GMP pilot plants.
- Transfer processes to other Sanofi sites.
- Provide technical support and expertise for transfers.
- Maintain assigned facilities.
- Adapt facilities for new projects.
- Collaborate with development units and GMP production.
- Collaborate with non-GMP PP Heads (USP and DSP).
- Represent non-GMP Pilot Plant in project teams.
- Represent non-GMP Pilot Plant in cross-functional initiatives.
- Stay current with specialized literature.
- Attend scientific congresses and training courses.
- Identify innovative processes and methods.
- Implement new knowledge in your area.
- Coordinate knowledge implementation with your supervisor.
Berufserfahrung
- 5 Jahre
Ausbildung
- Doktor / Ph.D.
Sprachen
- Deutsch – verhandlungssicher
- Englisch – verhandlungssicher
Tools & Technologien
- MS Office
Benefits
Gesundheits- & Fitnessangebote
- High-quality healthcare
Mentale Gesundheitsförderung
- Prevention programs
Sonstige Vorteile
- Coverage for long-term illness
Großzügige Elternzeit
- 14-week paid family leave
Kinderbetreuung
- Childcare benefits
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Sanofi-Aventis Deutschland GmbH erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
Noch nicht perfekt?
- Sanofi-Aventis Deutschland GmbH
DSP Process Engineer(m/w/x)
Vollzeitnur vor OrtSeniorFrankfurt am Main - Sanofi-Aventis Deutschland GmbH
Laboratory Head Upstream Process Development(m/w/x)
Vollzeitnur vor OrtBerufserfahrenFrankfurt am Main - Sanofi
Scientist high-throughput Biophysical Characterization(m/w/x)
Vollzeitnur vor OrtBerufserfahrenFrankfurt am Main - Sanofi-Aventis Deutschland GmbH
Scientist Protein Analytics(m/w/x)
Vollzeitnur vor OrtBerufserfahrenFrankfurt am Main
SASanofi-Aventis Deutschland GmbH
Scientist - Tech Area(m/w/x)
Frankfurt am Main
VollzeitVor OrtSenior
AI/ML
Nejo KI-Zusammenfassung
Scaling microbial projects for non-GMP drug substance production, implementing new continuous process technologies and AI solutions at a cardiovascular medicine developer. Experience in production (USP) and purification (DSP) of biologics with microbial systems required; mammalian cell culture experience beneficial. 14-week paid family leave, childcare benefits.
Anforderungen
- Advanced university degree (PhD/similar) in Natural Sciences/Engineering (Biology, Biotechnology, Chemical Engineering, or similar), or minimum 5 years professional experience
- Experience in production (USP) and purification (DSP) of biologics (microbial systems)
- Beneficial experience with mammalian cell culture
- Experience in scale-up and continuous production processes
- Experience in identification, evaluation, implementation of new technologies
- Experience in international/interdisciplinary project management
- Strong teamwork and communication skills
- Excellent organizational skills
- Collaborative spirit for cross-functional exchange
- Independent work style and solution-oriented approach
- High self-motivation, reliability, and responsibility
- Pioneering spirit and willingness to learn
- Knowledge/experience with biological product production processes (proteins, plasmids)
- Process engineering understanding; cultivation/purification scale-up knowledge
- Knowledge of continuous production processes
- Knowledge in bioanalytics
- Knowledge in process digitalization
- Beneficial programming skills, data analysis tools, multivariate data analysis know-how
- Analytical thinking and approach
- Very good IT skills (MS Office), knowledge of IT-supported plant systems
Aufgaben
- Support non-GMP production (USP) of microbial drug substance.
- Support non-GMP purification (DSP) of microbial drug substance.
- Identify and evaluate new technical scale technologies.
- Implement new technical scale technologies.
- Pioneer continuous and disposable production processes.
- Assess feasibility of GMP facilities.
- Evaluate GMP facility robustness and performance.
- Select or design new production facilities.
- Plan microbial projects at non-GMP technical scale.
- Scale up microbial projects at non-GMP technical scale.
- Supply technical material for microbial projects.
- Analyze technical material for microbial projects.
- Troubleshoot microbial projects at non-GMP technical scale.
- Characterize and evaluate equipment.
- Develop predictive models for continuous processes.
- Develop predictive models for process scalability.
- Introduce electronic systems and AI solutions.
- Digitalize processes, workflows, and documentation.
- Digitalize analysis of process-relevant production data.
- Organize and coordinate lab and process procedures.
- Optimize lab and process procedures.
- Ensure compliance with guidelines and safety regulations.
- Establish protocols and safety evaluations.
- Establish working procedures.
- Plan and execute experiments.
- Develop and document experiments.
- Incorporate in-process analytical methods.
- Ensure efficient and documented process transfer.
- Transfer processes to GMP pilot plants.
- Transfer processes to other Sanofi sites.
- Provide technical support and expertise for transfers.
- Maintain assigned facilities.
- Adapt facilities for new projects.
- Collaborate with development units and GMP production.
- Collaborate with non-GMP PP Heads (USP and DSP).
- Represent non-GMP Pilot Plant in project teams.
- Represent non-GMP Pilot Plant in cross-functional initiatives.
- Stay current with specialized literature.
- Attend scientific congresses and training courses.
- Identify innovative processes and methods.
- Implement new knowledge in your area.
- Coordinate knowledge implementation with your supervisor.
Berufserfahrung
- 5 Jahre
Ausbildung
- Doktor / Ph.D.
Sprachen
- Deutsch – verhandlungssicher
- Englisch – verhandlungssicher
Tools & Technologien
- MS Office
Benefits
Gesundheits- & Fitnessangebote
- High-quality healthcare
Mentale Gesundheitsförderung
- Prevention programs
Sonstige Vorteile
- Coverage for long-term illness
Großzügige Elternzeit
- 14-week paid family leave
Kinderbetreuung
- Childcare benefits
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Sanofi-Aventis Deutschland GmbH erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
Über das Unternehmen
Sanofi-Aventis Deutschland GmbH
Branche
Pharmaceuticals
Beschreibung
Das Unternehmen bietet Arzneimittel zur Prävention von Herz-Kreislauf-Erkrankungen an und setzt sich für die Verbesserung der Lebensqualität ein.
Noch nicht perfekt?
- Sanofi-Aventis Deutschland GmbH
Laboratory Head non-GMP PP Tech Area(m/w/x)
Vollzeitnur vor OrtSeniorFrankfurt am Main - Sanofi-Aventis Deutschland GmbH
DSP Process Engineer(m/w/x)
Vollzeitnur vor OrtSeniorFrankfurt am Main - Sanofi-Aventis Deutschland GmbH
Laboratory Head Upstream Process Development(m/w/x)
Vollzeitnur vor OrtBerufserfahrenFrankfurt am Main - Sanofi
Scientist high-throughput Biophysical Characterization(m/w/x)
Vollzeitnur vor OrtBerufserfahrenFrankfurt am Main - Sanofi-Aventis Deutschland GmbH
Scientist Protein Analytics(m/w/x)
Vollzeitnur vor OrtBerufserfahrenFrankfurt am Main