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Neogen Corporation

Senior Research Scientist

Neogen Corporation

. Lead scientific design and hands-on laboratory development of rapid nucleic acid-based methods for detecting and differentiating foodborne pathogens.

Posted 10/5/2026full-timeLansing • Michigan • United StatesSeniorWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in designing, optimizing, and troubleshooting nucleic acid-based assays, with a strong foundation in molecular biology and bioinformatics. Capable of leading complex technical projects and collaborating across teams to develop practical molecular detection solutions.

Highest-signal resume keywords
Nucleic Acid-Based Assay DevelopmentBioinformatics ToolsLaboratory Experience with Foodborne PathogensStatistical Methods in Assay PerformanceTechnical Leadership and Communication

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Assay DesignTroubleshootingPrimer/Probe DesignMultiplex Assay DevelopmentAnalytical Performance StudiesSensitivity and Specificity AnalysisExperimental DesignMolecular TestingData InterpretationGenomic Data Analysis
Soft Skills
Scientific CommunicationMentoringCollaborationDecision MakingTechnical Report Writing
Tools & Technologies
NCBI GenBankRefSeqSRAGenomeTrakrEnteroBase
Industry Keywords
Foodborne PathogensMolecular BiologyMicrobiologyGenomicsBioinformaticsAOACISOMicroValUSDA-FSISFDA

About the role

Key responsibilities & impact
  • Lead scientific design and hands-on laboratory development of rapid nucleic acid-based methods for detecting and differentiating foodborne pathogens.
  • Plan and execute laboratory studies, analyze results, troubleshoot assay performance, and guide subsequent development.
  • Design, optimize, and troubleshoot assays using relevant amplification technologies; evaluate controls, specificity, sensitivity, robustness, and contamination risks.
  • Perform pathogen laboratory studies, including culture preparation, enrichment, inoculation, molecular testing, and interpretation of results.
  • Apply statistical methods to study design, sampling plans, acceptance criteria, and assay-performance analysis.
  • Use bioinformatics tools, genomic data, and sequence-analysis approaches for target selection, assay design, and performance interpretation.
  • Lead and support verification and validation studies, protocols, evidence packages, and applicable AOAC, ISO, MicroVal, USDA-FSIS, or FDA pathways.
  • Collaborate with Product Development, Engineering, Quality, Regulatory, Operations, and Commercial teams through feasibility, development, transfer, launch, and continuous improvement.
  • Provide technical leadership, communicate scientific evidence and risk, review technical work, mentor colleagues, and contribute to scientific collaborations.
  • Travel up to 5% for partner studies, technical meetings, or scientific events.

Requirements

What you’ll need
  • Bachelor’s degree in Molecular Biology, Microbiology, Genomics, Bioinformatics, Biochemistry, or a related scientific discipline with at least 8 years of relevant experience; Master’s degree with at least 6 years of relevant experience; or Ph.D. with at least 3 years of relevant experience.
  • Demonstrated experience designing, optimizing, and troubleshooting nucleic acid-based assays, including primer/probe design, assay controls, multiplex assay development, and interpretation of amplification data.
  • Strong experience using bioinformatics, comparative genomics, and sequence-analysis tools.
  • Substantial hands-on laboratory experience developing and troubleshooting molecular assays using foodborne pathogens or closely related microbial systems.
  • Experience planning, executing, and interpreting analytical performance studies, including sensitivity, specificity, robustness, repeatability, reproducibility, and limit-of-detection studies.
  • Experience using public and commercial genomic resources, including NCBI GenBank, RefSeq, SRA, GenomeTrakr, and EnteroBase.
  • Working knowledge of applied statistics and experimental design used in assay development and performance evaluation.
  • Ability to lead complex technical projects, make evidence-based decisions, and translate scientific findings into practical molecular detection solutions.
  • Strong written and verbal scientific communication skills, including technical reports, protocols, presentations, publications, and cross-functional decision support.
  • Employment authorization to work in the United States.
  • Employment contingent upon successful completion of applicable pre-employment requirements and verification of identity and authorization to work in the United States.

Benefits

Comp & perks
  • Benefits starting on Day One – Medical, dental, and vision coverage begin on your first day of employment.
  • 401(k) with company match
  • Paid Time Off (PTO)
  • Career Growth Opportunities, including tools, training, and support
  • Meaningful work with impact on customers, communities, and the world
  • Collaborative culture valuing innovation, respect, teamwork, and continuous improvement