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Scientist I – Bioassay Sciences and Development(m/w/x)
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.
Requirements
- 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
Tasks
- 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.
Work Experience
- 2 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
- German – Business Fluent
Tools & Technologies
- mRNA lipid nanoparticles
- PCR
- FACS
- SPR
- electronic laboratory notebooks
- regulated documentation systems
Benefits
Informal Culture
- Diverse work environment
- Open corporate culture
- Great Place to Work recognition
- Inclusive culture
Purpose-Driven Work
- Real impact
Mentorship & Coaching
- Intensive onboarding process
- Mentor support
Flexible Working
- Flexible work models
- Healthy work-life balance
Healthcare & Fitness
- Corporate health management
- Comprehensive health programs
- Exercise programs
Other Benefits
- Company social benefits
- International organization
- Equality, equity, diversity and inclusion commitment
Career Advancement
- Wide career opportunities
- Strong international network
Learning & Development
- Top-tier development opportunities
Not a perfect match?
- AbbVieFull-time/Part-timeOn-siteExperiencedLudwigshafen am Rhein
- Octapharma Biopharmaceuticals GmbH
Scientist R&D Molecular Design(m/w/x)
Full-timeOn-siteExperiencedHeidelberg - AbbVie
Principal Research Scientist I/II / Biologics Drug Product Lead (R&D)(m/w/x)
Full-timeOn-siteSeniorLudwigshafen am Rhein - AGC Biologics GmbH
Team Leader Process Development - Nucleic Acids (pDNA & mRNA)(m/w/x)
Full-timeOn-siteSeniorHeidelberg - AbbVie
Bench Scientist II / Senior Bench Scientist I – Mass Spectrometry & Characterization of Therapeutic Proteins(m/w/x)
Full-timeOn-siteSeniorLudwigshafen am Rhein
Scientist I – Bioassay Sciences and Development(m/w/x)
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.
Requirements
- 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
Tasks
- 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.
Work Experience
- 2 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
- German – Business Fluent
Tools & Technologies
- mRNA lipid nanoparticles
- PCR
- FACS
- SPR
- electronic laboratory notebooks
- regulated documentation systems
Benefits
Informal Culture
- Diverse work environment
- Open corporate culture
- Great Place to Work recognition
- Inclusive culture
Purpose-Driven Work
- Real impact
Mentorship & Coaching
- Intensive onboarding process
- Mentor support
Flexible Working
- Flexible work models
- Healthy work-life balance
Healthcare & Fitness
- Corporate health management
- Comprehensive health programs
- Exercise programs
Other Benefits
- Company social benefits
- International organization
- Equality, equity, diversity and inclusion commitment
Career Advancement
- Wide career opportunities
- Strong international network
Learning & Development
- Top-tier development opportunities
About the Company
AbbVie
Industry
Pharmaceuticals
Description
Das Unternehmen setzt sich für die Entdeckung und Bereitstellung innovativer Medikamente und Lösungen ein, die ernsthafte Gesundheitsprobleme lösen.
Not a perfect match?
- AbbVie
Scientist I – Bioassay Sciences and Development(m/w/x)
Full-time/Part-timeOn-siteExperiencedLudwigshafen am Rhein - Octapharma Biopharmaceuticals GmbH
Scientist R&D Molecular Design(m/w/x)
Full-timeOn-siteExperiencedHeidelberg - AbbVie
Principal Research Scientist I/II / Biologics Drug Product Lead (R&D)(m/w/x)
Full-timeOn-siteSeniorLudwigshafen am Rhein - AGC Biologics GmbH
Team Leader Process Development - Nucleic Acids (pDNA & mRNA)(m/w/x)
Full-timeOn-siteSeniorHeidelberg - AbbVie
Bench Scientist II / Senior Bench Scientist I – Mass Spectrometry & Characterization of Therapeutic Proteins(m/w/x)
Full-timeOn-siteSeniorLudwigshafen am Rhein