6 дней назад
Research Associate (Bioanalytical Research)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Research Associate (Bioanalytical Research): Conducting and validating ligand binding assay experiments for pharmacokinetic and anti-drug antibody studies with an accent on biological sample analysis, assay documentation, and laboratory information management. Focus on analyzing results in LIMS, Excel, and GraphPad Prism, maintaining laboratory equipment and reagents, and supporting compliant laboratory and environmental safety practices.
Location: Berlin, Germany; onsite laboratory role
Company
provides research and laboratory services supporting precision medicine and drug development programs.
What you will do
- Plan, perform, establish, analyze, and validate bioanalytical experiments using ligand binding assay formats.
- Conduct biological sample analyses for pharmacokinetic and anti-drug antibody studies, including PK, ADA, TAb, and NAb assays.
- Analyze and aggregate experimental results in LIMS, Microsoft Excel, and GraphPad Prism for reports and development updates.
- Review and maintain SOPs, validation protocols, reports, LIMS experiment protocols, templates, and related documentation.
- Maintain laboratory equipment, reagents, materials, inventories, and waste-handling processes.
- Support method development, laboratory information management processes, and laboratory and environmental safety practices.
Requirements
- Experience or capability in ligand binding assay-based bioanalytical experimentation and biological sample analysis.
- Ability to work with LIMS, Microsoft Excel, and GraphPad Prism.
- Ability to follow training, SOPs, validation documentation, and department procedures.
- Ability to maintain equipment, reagents, materials, and laboratory records.
- Must be legally authorized to work in Germany without employer sponsorship.
Culture & Benefits
- Work in a laboratory environment supporting precision medicine and drug development studies.
- Participate in method development, validation, documentation, and continuous improvement activities.
- Follow established laboratory, environmental, and safety procedures.
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