Die KI-Suchmaschine für Jobs
DSP Process Engineer(m/w/x)
Beschreibung
As a DSP Process Engineer, you will engage in scaling and optimizing biopharmaceutical production processes, collaborating with various teams to implement innovative technologies and ensure compliance with safety regulations. This role involves hands-on experimentation and the transfer of developed processes to GMP environments.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •University degree (Master's/Diploma) in Biotechnology, Process Engineering, Biochemistry, or comparable field
- •Several years of professional experience in the biopharmaceutical industry, ideally in purification of proteins with different chromatographic techniques, separation/filtration, ultrafiltration/diafiltration from lab to tech scale
- •Experience in bioconjugation and click-chemistry
- •Strong teamwork and communication skills
- •Excellent organizational skills
- •Collaborative spirit for open exchange in crossfunctional teams
- •Independent work style and solution-oriented approach
- •High self-motivation, reliability, and sense of responsibility
- •Pioneering spirit and willingness to continuously learn
- •Extensive knowledge and professional experience with production processes for biological products, particularly in purification techniques for various modalities
- •Process engineering understanding and knowledge in scale-up of purification processes
- •Experience in programming / working with Process control Systems, software for data handling, electronic batch records, etc.
- •Expertise in programming or/and multivariate data analysis beneficial
- •Knowledge in bioanalytics
- •Analytical thinking and approach
- •Very good IT skills (MS Office) and knowledge in handling modern, IT-supported plant systems
- •Excellent German and English skills, both written and spoken
Ausbildung
Berufserfahrung
ca. 4 - 6 Jahre
Aufgaben
- •Plan and execute purification of technical materials
- •Troubleshoot and implement technology for microbial projects
- •Scale up processes and characterize technical equipment
- •Provide technical expertise to global downstream project teams
- •Support the introduction of electronic systems and AI solutions
- •Evaluate and implement new technologies in collaboration with Lab Head
- •Organize and optimize lab and process procedures per guidelines
- •Establish documentation including protocols and safety evaluations
- •Lead pilot plant activities functionally
- •Collaborate closely with development units and GMP production
- •Plan, execute, and document experiments with analytical methods
- •Ensure efficient transfer of processes to GMP pilot plants
- •Maintain assigned facilities and adapt them for new projects
Tools & Technologien
Sprachen
Deutsch – verhandlungssicher
Englisch – verhandlungssicher
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
- Sanofi-Aventis Deutschland GmbHVollzeitnur vor OrtSeniorFrankfurt am Main
- Sanofi-Aventis Deutschland GmbH
Laboratory Head non-GMP PP Tech Area(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 - Formo Bio GmbH
Research Associate - Downstream Processing(m/w/x)
Vollzeitnur vor OrtBerufserfahrenFrankfurt am Main - Formo Bio GmbH
Upstream Processing Scientist(m/w/x)
Vollzeitnur vor OrtBerufserfahrenFrankfurt am Main
DSP Process Engineer(m/w/x)
Die KI-Suchmaschine für Jobs
Beschreibung
As a DSP Process Engineer, you will engage in scaling and optimizing biopharmaceutical production processes, collaborating with various teams to implement innovative technologies and ensure compliance with safety regulations. This role involves hands-on experimentation and the transfer of developed processes to GMP environments.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •University degree (Master's/Diploma) in Biotechnology, Process Engineering, Biochemistry, or comparable field
- •Several years of professional experience in the biopharmaceutical industry, ideally in purification of proteins with different chromatographic techniques, separation/filtration, ultrafiltration/diafiltration from lab to tech scale
- •Experience in bioconjugation and click-chemistry
- •Strong teamwork and communication skills
- •Excellent organizational skills
- •Collaborative spirit for open exchange in crossfunctional teams
- •Independent work style and solution-oriented approach
- •High self-motivation, reliability, and sense of responsibility
- •Pioneering spirit and willingness to continuously learn
- •Extensive knowledge and professional experience with production processes for biological products, particularly in purification techniques for various modalities
- •Process engineering understanding and knowledge in scale-up of purification processes
- •Experience in programming / working with Process control Systems, software for data handling, electronic batch records, etc.
- •Expertise in programming or/and multivariate data analysis beneficial
- •Knowledge in bioanalytics
- •Analytical thinking and approach
- •Very good IT skills (MS Office) and knowledge in handling modern, IT-supported plant systems
- •Excellent German and English skills, both written and spoken
Ausbildung
Berufserfahrung
ca. 4 - 6 Jahre
Aufgaben
- •Plan and execute purification of technical materials
- •Troubleshoot and implement technology for microbial projects
- •Scale up processes and characterize technical equipment
- •Provide technical expertise to global downstream project teams
- •Support the introduction of electronic systems and AI solutions
- •Evaluate and implement new technologies in collaboration with Lab Head
- •Organize and optimize lab and process procedures per guidelines
- •Establish documentation including protocols and safety evaluations
- •Lead pilot plant activities functionally
- •Collaborate closely with development units and GMP production
- •Plan, execute, and document experiments with analytical methods
- •Ensure efficient transfer of processes to GMP pilot plants
- •Maintain assigned facilities and adapt them for new projects
Tools & Technologien
Sprachen
Deutsch – verhandlungssicher
Englisch – verhandlungssicher
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
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.
- Sanofi-Aventis Deutschland GmbH
Scientist non-GMP PP Tech Area(m/w/x)
Vollzeitnur vor OrtSeniorFrankfurt am Main - Sanofi-Aventis Deutschland GmbH
Laboratory Head non-GMP PP Tech Area(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 - Formo Bio GmbH
Research Associate - Downstream Processing(m/w/x)
Vollzeitnur vor OrtBerufserfahrenFrankfurt am Main - Formo Bio GmbH
Upstream Processing Scientist(m/w/x)
Vollzeitnur vor OrtBerufserfahrenFrankfurt am Main