AbbVie
Scientist I – Bioassay Sciences and Development(m/w/x)
Full-time/Part-timeOn-siteExperienced
Ludwigshafen am Rhein
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ABAbbVie
Scientist I – Bioassay Sciences and Development(m/w/x)
Ludwigshafen am Rhein
Full-time, Part-timeOn-siteExperienced
Nejo AI Summary
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
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of AbbVie and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
Not a perfect match?
- Octapharma Biopharmaceuticals GmbH
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Principal Research Scientist I/II / Biologics Drug Product Lead (R&D)(m/w/x)
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ABAbbVie
Scientist I – Bioassay Sciences and Development(m/w/x)
Ludwigshafen am Rhein
Full-time, Part-timeOn-siteExperienced
Nejo AI Summary
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
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of AbbVie and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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 - AbbVie
Scientist II Commercial Design Verification Testing (DVT)(m/w/x)
Full-timeOn-siteExperiencedLudwigshafen am Rhein - AGC Biologics GmbH
Team Leader Process Development - Nucleic Acids (pDNA & mRNA)(m/w/x)
Full-timeOn-siteSeniorHeidelberg