Senior Pathology Assay Scientist – Tissue Biomarkers

MacroGenics, Inc.

Rockville (MD)

Sur place

USD 101 000 - 176 000

Plein temps

14 jours+

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Résumé du poste

MacroGenics, Inc. is seeking a Sr. Scientist I/II in Pathology Assay Development to lead tissue-based biomarker assay development supporting ADC and immunotherapy programs from discovery through early clinical development.

Focus areas include single-plex and multiplex IHC/IF, ISH, digital pathology and tissue workflows. You will work with cross-functional teams to generate robust biomarker data, troubleshoot assays, coordinate external CROs, and contribute to publications and regulatory

Qualifications

  • Hands-on experience developing tissue-based biomarker assays (IHC, multiplex IF) in biotech, pharma, or CRO settings.
  • Experience with FFPE and frozen tissue handling and assay controls; artifact awareness.
  • Experience designing qualification/validation studies and setting objective criteria.

Responsabilités

  • Independently develop, optimize, qualify, validate, and troubleshoot single-plex IHC, multiplex IHC/IF, and ISH assays.
  • Coordinate assay development plans including antibody selection, titration, and controls.
  • Perform digital pathology review and quantitative analysis to generate robust biomarker data.
  • Collaborate with external CROs/central labs for assay transfer and concordance activities.

Connaissances

Tissue-based biomarker assays
IHC
Multiplex IHC/IF
Digital pathology

Formation

PhD in relevant field
MS in relevant field
BS in relevant field

Outils

HALO
QuPath
Visiopharm

Description du poste

MacroGenics, Inc. is seeking a Sr. Scientist I/II in Pathology Assay Development to lead tissue-based biomarker assay development supporting ADC and immunotherapy programs from discovery through early clinical development.

Focus areas include single-plex and multiplex IHC/IF, ISH, digital pathology and tissue workflows. You will work with cross-functional teams to generate robust biomarker data, troubleshoot assays, coordinate external CROs, and contribute to publications and regulatory

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