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Scientist I – Bioassay Sciences and Development(m/w/x)
Developing and validating cell bioassays, qPCR, and ddPCR for genetic medicine technologies, with GMP reagent qualification at a global pharma firm. Experience with genetic medicine technologies (PCR, FACS, SPR) highly desirable. Intensive onboarding, dedicated mentor support.
Anforderungen
- Bachelor's (5 years experience) or Master's (2 years 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 technological advancements in laboratory automation
- Experience developing/validating binding and cell-based assays
- Strong organizational skills
- Strong presentation skills
- Strong cross-functional teamwork skills
- Strong networking skills
- Experience with electronic laboratory notebooks and regulated documentation systems
- Excellent written/verbal communication skills in English
- Excellent written/verbal communication skills in German
Aufgaben
- Design, optimize, transfer cell bioassays.
- Design, optimize, transfer qPCR and ddPCR.
- Independently qualify reagents under GMP.
- Independently validate assays for release studies.
- Independently analyze samples for stability studies.
- Independently transfer test methods for tLNP development.
- Author laboratory reports in English.
- Author Standard Operating Procedures (SOPs).
- Author automated system documentation.
- Author development and validation reports.
- Coordinate GMP-relevant laboratory tasks.
- Serve as equipment subject matter expert.
- Oversee equipment qualification.
- Communicate effectively 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
- potency assays
- PCR
- FACS
- SPR
- electronic laboratory notebooks
- regulated documentation systems
Benefits
Lockere Unternehmenskultur
- Diverse work environment
- Open corporate 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
Karriere- und Weiterentwicklung
- Wide range of career opportunities
- Top-tier, attractive development opportunities
- Strong international network
Noch nicht perfekt?
- AbbVieVollzeit/Teilzeitnur vor OrtBerufserfahrenLudwigshafen am Rhein
- Octapharma Biopharmaceuticals GmbH
Scientist R&D Molecular Design(m/w/x)
Vollzeitnur vor OrtBerufserfahrenHeidelberg - AbbVie
Scientist II Commercial Design Verification Testing (DVT)(m/w/x)
Vollzeitnur vor OrtBerufserfahrenLudwigshafen am Rhein - AbbVie
Principal Research Scientist I/II / Biologics Drug Product Lead (R&D)(m/w/x)
Vollzeitnur vor OrtSeniorLudwigshafen am Rhein - AbbVie
Principal Research Scientist I/II / Biologics Drug Product Lead (R&D)(m/w/x)
Vollzeitnur vor OrtSeniorLudwigshafen am Rhein
Scientist I – Bioassay Sciences and Development(m/w/x)
Developing and validating cell bioassays, qPCR, and ddPCR for genetic medicine technologies, with GMP reagent qualification at a global pharma firm. Experience with genetic medicine technologies (PCR, FACS, SPR) highly desirable. Intensive onboarding, dedicated mentor support.
Anforderungen
- Bachelor's (5 years experience) or Master's (2 years 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 technological advancements in laboratory automation
- Experience developing/validating binding and cell-based assays
- Strong organizational skills
- Strong presentation skills
- Strong cross-functional teamwork skills
- Strong networking skills
- Experience with electronic laboratory notebooks and regulated documentation systems
- Excellent written/verbal communication skills in English
- Excellent written/verbal communication skills in German
Aufgaben
- Design, optimize, transfer cell bioassays.
- Design, optimize, transfer qPCR and ddPCR.
- Independently qualify reagents under GMP.
- Independently validate assays for release studies.
- Independently analyze samples for stability studies.
- Independently transfer test methods for tLNP development.
- Author laboratory reports in English.
- Author Standard Operating Procedures (SOPs).
- Author automated system documentation.
- Author development and validation reports.
- Coordinate GMP-relevant laboratory tasks.
- Serve as equipment subject matter expert.
- Oversee equipment qualification.
- Communicate effectively 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
- potency assays
- PCR
- FACS
- SPR
- electronic laboratory notebooks
- regulated documentation systems
Benefits
Lockere Unternehmenskultur
- Diverse work environment
- Open corporate 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
Karriere- und Weiterentwicklung
- Wide range of career opportunities
- Top-tier, attractive development opportunities
- Strong international network
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
Scientist II Commercial Design Verification Testing (DVT)(m/w/x)
Vollzeitnur vor OrtBerufserfahrenLudwigshafen am Rhein - AbbVie
Principal Research Scientist I/II / Biologics Drug Product Lead (R&D)(m/w/x)
Vollzeitnur vor OrtSeniorLudwigshafen am Rhein - AbbVie
Principal Research Scientist I/II / Biologics Drug Product Lead (R&D)(m/w/x)
Vollzeitnur vor OrtSeniorLudwigshafen am Rhein