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Scientist I
EurofinsScientist I executing and supporting development of cell-based bioassays in GMP laboratory. Collaborating across projects to generate high-quality data for pharmaceutical product testing.
Posted 7/29/2026full-timeRemote • California • 🇺🇸 United StatesJuniorMid-Level💰 $40,000 - $60,000 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in executing and supporting cell-based bioassays within a GMP-regulated environment, including proficiency in mammalian cell culture, assay development, and data analysis. Strong technical writing skills and experience with quality systems and regulatory compliance are essential.
Highest-signal resume keywords
Mammalian Cell CultureCell-Based Assay ExecutionGMP Assay ValidationData Analysis and InterpretationTechnical Writing and Documentation
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
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Hard Skills
Cell-Based Potency AssaysELISA AssaysFlow CytometryStatistical AnalysisAssay OptimizationAseptic TechniqueGMP ComplianceQuality ControlTroubleshootingMethod Transfer
Soft Skills
CollaborationCommunicationProblem-Solving
Tools & Technologies
GraphPad PrismSoftMax ProJMPPLAMicrosoft Excel
Industry Keywords
GMPGLPGDPALCOA+BiotechnologyImmunologyMolecular BiologyBiochemistryCell BiologyQuality Systems
About the role
Key responsibilities & impact- Execute and support the development, qualification, validation, and transfer of cell-based bioassays in a GMP-regulated laboratory environment
- Perform cell-based potency, functional, neutralization, reporter gene, proliferation, viability, and ELISA assays
- Maintain mammalian cell cultures and prepare reagents, standards, and controls
- Execute GMP release, stability, characterization, and comparability studies
- Monitor assay performance using established system suitability criteria and control trending
- Support assay development, optimization, qualification, validation, and method transfer activities
- Execute studies assessing precision, accuracy, specificity, linearity, range, robustness, and system suitability
- Analyze data using bioassay and statistical software
- Author and review protocols, reports, SOPs, and technical summaries
- Perform work in accordance with GMP, GDP, GLP, ALCOA+, and established quality systems
- Participate in deviations, OOS/OOT investigations, CAPAs, and change controls
- Collaborate with project managers, QA, study directors, and scientific staff
Requirements
What you’ll need- BS or MS in Biology, Cell Biology, Immunology, Biochemistry, Biotechnology, Molecular Biology, or related scientific discipline
- BS with 2–4 years or MS with 1–2 years of relevant laboratory experience in industry settings
- Experience with mammalian cell culture, ELISA, flow cytometry, or cell-based assays preferred
- Mammalian cell culture and aseptic technique
- Cell-based assay execution and troubleshooting
- Data analysis and interpretation
- Technical writing and documentation
- Proficiency with Microsoft Excel and scientific software
- Preferred: Cell-based potency, reporter gene, ADCC, and neutralization assays; ELISA, flow cytometry, and ligand-binding assays; qPCR/ddPCR methods; GraphPad Prism, SoftMax Pro, PLA, JMP, or similar software; GMP assay validation experience
Benefits
Comp & perks- Excellent full time benefits including comprehensive medical coverage, dental, and vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holiday