AbbVie
Scientist I – Bioassay Sciences and Development(m/w/x)
Vollzeit/Teilzeitnur vor OrtBerufserfahren
Ludwigshafen am Rhein
Neuer Job?Nejo!
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ABAbbVie
Scientist I – Bioassay Sciences and Development(m/w/x)
Ludwigshafen am Rhein
Vollzeit, TeilzeitVor OrtBerufserfahren
Nejo KI-Zusammenfassung
Advancing targeted mRNA lipid nanoparticles and automating assays in a GMP environment. Bachelor's with 5 years or Master's with 2 years experience in scientific field required. Formal mentor support program.
Anforderungen
- Bachelor's degree (plus 5 years relevant experience) or Master's degree (plus 2 years relevant experience) in scientific/technical field, or equivalent professional experience
- Experience with mRNA lipid nanoparticles and potency assays (plus)
- Experience with genetic medicine technologies (PCR, FACS, SPR) (highly desirable)
- Strong analytical ability, innovative mindset, excellent problem-solving skills, curiosity for lab automation advancements
- Experience developing/validating binding and cell-based assays for biomolecules
- Strong organizational, presentation, cross-functional teamwork, and networking skills
- Experience with electronic lab notebooks and regulated documentation systems
- Excellent written and verbal communication skills in English and German
Aufgaben
- Advance efforts on targeted mRNA lipid nanoparticles.
- Translate scientific innovation into operational standards.
- Automate assays in a GMP compliant environment.
- Execute assays for running programs.
- Verify data for running programs.
- Optimize new modalities and technologies.
- Integrate new modalities and technologies.
- Implement expression assays.
- Implement functional potency assays.
- Implement PCR applications.
- Characterize innovative therapeutics.
- Perform quality control on innovative therapeutics.
- Design, optimize, and transfer cell-based bioassays.
- Design, optimize, and transfer qPCR and ddPCR technologies.
- Qualify reagents independently under GMP.
- Validate assays under GMP.
- Analyze samples for release and stability studies.
- Transfer test methods under GMP.
- Author laboratory reports.
- Author Standard Operating Procedures (SOPs) in English.
- Document automated systems.
- Author development and validation reports.
- Coordinate GMP-relevant laboratory tasks.
- Serve as equipment subject matter expert.
- Oversee equipment qualification.
- Communicate in meetings and teleconferences.
- Collaborate across sites and departments.
- Promote best practices in laboratory automation.
Berufserfahrung
- 2 Jahre
Ausbildung
- Bachelor-AbschlussODER
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
- Deutsch – verhandlungssicher
Tools & Technologien
- mRNA lipid nanoparticles
- PCR
- FACS
- SPR
- electronic laboratory notebooks
- regulated documentation systems
Benefits
Lockere Unternehmenskultur
- Diverse work environment
- Open corporate culture
- Great Place to Work recognition
- Inclusive culture
Sinnstiftende Arbeit
- Real impact
Mentoring & Coaching
- Intensive onboarding process
- Mentor support
Flexibles Arbeiten
- Flexible work models
- Healthy work-life balance
Gesundheits- & Fitnessangebote
- Corporate health management
- Comprehensive health programs
- Exercise programs
Sonstige Vorteile
- Company social benefits
- International organization
- Equality, equity, diversity and inclusion commitment
Karriere- und Weiterentwicklung
- Wide career opportunities
- Strong international network
Weiterbildungsangebote
- Top-tier development opportunities
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens AbbVie 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?
- Octapharma Biopharmaceuticals GmbH
Scientist R&D Molecular Design(m/w/x)
Vollzeitnur vor OrtBerufserfahrenHeidelberg - AbbVie
Principal Research Scientist I/II / Biologics Drug Product Lead (R&D)(m/w/x)
Vollzeitnur vor OrtSeniorLudwigshafen am Rhein - AbbVie
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Vollzeitnur vor OrtBerufserfahrenLudwigshafen am Rhein - AGC Biologics GmbH
Team Leader Process Development - Nucleic Acids (pDNA & mRNA)(m/w/x)
Vollzeitnur vor OrtSeniorHeidelberg
ABAbbVie
Scientist I – Bioassay Sciences and Development(m/w/x)
Ludwigshafen am Rhein
Vollzeit, TeilzeitVor OrtBerufserfahren
Nejo KI-Zusammenfassung
Advancing targeted mRNA lipid nanoparticles and automating assays in a GMP environment. Bachelor's with 5 years or Master's with 2 years experience in scientific field required. Formal mentor support program.
Anforderungen
- Bachelor's degree (plus 5 years relevant experience) or Master's degree (plus 2 years relevant experience) in scientific/technical field, or equivalent professional experience
- Experience with mRNA lipid nanoparticles and potency assays (plus)
- Experience with genetic medicine technologies (PCR, FACS, SPR) (highly desirable)
- Strong analytical ability, innovative mindset, excellent problem-solving skills, curiosity for lab automation advancements
- Experience developing/validating binding and cell-based assays for biomolecules
- Strong organizational, presentation, cross-functional teamwork, and networking skills
- Experience with electronic lab notebooks and regulated documentation systems
- Excellent written and verbal communication skills in English and German
Aufgaben
- Advance efforts on targeted mRNA lipid nanoparticles.
- Translate scientific innovation into operational standards.
- Automate assays in a GMP compliant environment.
- Execute assays for running programs.
- Verify data for running programs.
- Optimize new modalities and technologies.
- Integrate new modalities and technologies.
- Implement expression assays.
- Implement functional potency assays.
- Implement PCR applications.
- Characterize innovative therapeutics.
- Perform quality control on innovative therapeutics.
- Design, optimize, and transfer cell-based bioassays.
- Design, optimize, and transfer qPCR and ddPCR technologies.
- Qualify reagents independently under GMP.
- Validate assays under GMP.
- Analyze samples for release and stability studies.
- Transfer test methods under GMP.
- Author laboratory reports.
- Author Standard Operating Procedures (SOPs) in English.
- Document automated systems.
- Author development and validation reports.
- Coordinate GMP-relevant laboratory tasks.
- Serve as equipment subject matter expert.
- Oversee equipment qualification.
- Communicate in meetings and teleconferences.
- Collaborate across sites and departments.
- Promote best practices in laboratory automation.
Berufserfahrung
- 2 Jahre
Ausbildung
- Bachelor-AbschlussODER
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
- Deutsch – verhandlungssicher
Tools & Technologien
- mRNA lipid nanoparticles
- PCR
- FACS
- SPR
- electronic laboratory notebooks
- regulated documentation systems
Benefits
Lockere Unternehmenskultur
- Diverse work environment
- Open corporate culture
- Great Place to Work recognition
- Inclusive culture
Sinnstiftende Arbeit
- Real impact
Mentoring & Coaching
- Intensive onboarding process
- Mentor support
Flexibles Arbeiten
- Flexible work models
- Healthy work-life balance
Gesundheits- & Fitnessangebote
- Corporate health management
- Comprehensive health programs
- Exercise programs
Sonstige Vorteile
- Company social benefits
- International organization
- Equality, equity, diversity and inclusion commitment
Karriere- und Weiterentwicklung
- Wide career opportunities
- Strong international network
Weiterbildungsangebote
- Top-tier development opportunities
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens AbbVie 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
AbbVie
Branche
Pharmaceuticals
Beschreibung
Das Unternehmen setzt sich für die Entdeckung und Bereitstellung innovativer Medikamente und Lösungen ein, die ernsthafte Gesundheitsprobleme lösen.
Noch nicht perfekt?
- AbbVie
Scientist I – Bioassay Sciences and Development(m/w/x)
Vollzeit/Teilzeitnur vor OrtBerufserfahrenLudwigshafen am Rhein - Octapharma Biopharmaceuticals GmbH
Scientist R&D Molecular Design(m/w/x)
Vollzeitnur vor OrtBerufserfahrenHeidelberg - AbbVie
Principal Research Scientist I/II / Biologics Drug Product Lead (R&D)(m/w/x)
Vollzeitnur vor OrtSeniorLudwigshafen am Rhein - AbbVie
Scientist II Commercial Design Verification Testing (DVT)(m/w/x)
Vollzeitnur vor OrtBerufserfahrenLudwigshafen am Rhein - AGC Biologics GmbH
Team Leader Process Development - Nucleic Acids (pDNA & mRNA)(m/w/x)
Vollzeitnur vor OrtSeniorHeidelberg