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
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.
Requirements
- 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
Tasks
- 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.
Work Experience
- 2 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
- German – Business Fluent
Tools & Technologies
- mRNA lipid nanoparticles
- potency assays
- PCR
- FACS
- SPR
- electronic laboratory notebooks
- regulated documentation systems
Benefits
Informal Culture
- Diverse work environment
- Open corporate 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
Career Advancement
- Wide range of career opportunities
- Top-tier, attractive development opportunities
- Strong international network
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.
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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
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.
Requirements
- 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
Tasks
- 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.
Work Experience
- 2 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
- German – Business Fluent
Tools & Technologies
- mRNA lipid nanoparticles
- potency assays
- PCR
- FACS
- SPR
- electronic laboratory notebooks
- regulated documentation systems
Benefits
Informal Culture
- Diverse work environment
- Open corporate 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
Career Advancement
- Wide range of career opportunities
- Top-tier, attractive development opportunities
- Strong international network
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
Scientist II Commercial Design Verification Testing (DVT)(m/w/x)
Full-timeOn-siteExperiencedLudwigshafen am Rhein - AbbVie
Principal Research Scientist I/II / Biologics Drug Product Lead (R&D)(m/w/x)
Full-timeOn-siteSeniorLudwigshafen am Rhein - AbbVie
Principal Research Scientist I/II / Biologics Drug Product Lead (R&D)(m/w/x)
Full-timeOn-siteSeniorLudwigshafen am Rhein