About The Position

SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has multiple assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials. SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discover and IND-enabling stages, representing cutting-edge biologics development. We offer an opportunity for you to learn and grow while making significant contributions to the company's success. We are seeking a highly organized and detail-oriented Research Associate I/II to support the development, optimization, and validation of immunohistochemistry (IHC) assays. This role will contribute to early-stage biomarker in support of clinical trial programs. The ideal candidate will have 2–3 years of hands-on industry experience in histology, IHC, or a regulated laboratory environment (e.g., CLIA/CAP, GLP). This is a bench-focused position requiring close collaboration with scientists, pathologists, and cross-functional project teams.

Requirements

  • BS or MS in Biology, Molecular Biology, Pathology, Biomedical Sciences, or a related field.
  • 1–3 years of hands-on experience in histology and/or IHC assay execution within a research or regulated diagnostic laboratory.
  • Experience handling FFPE tissues and operating automated IHC staining platforms.
  • Strong attention to detail with excellent documentation and record-keeping practices.
  • Ability to follow SOPs and work effectively in CLIA-, GxP-, or ISO-regulated environments.

Nice To Haves

  • Experience supporting IHC assay optimization and/or analytical validation studies.
  • Exposure to Akoya platforms and multiplex immunofluorescence projects.
  • Experience with digital pathology, slide scanning, or image analysis tools.
  • Knowledge of antibody characterization and tissue-based biomarker assay development.

Responsibilities

  • Perform tissue sectioning of FFPE blocks.
  • Route and support H&E staining workflows.
  • Perform routine IHC staining on FFPE tissue specimens using automated platforms (e.g., Ventana, Leica).
  • Conduct antibody titrations, protocol optimization, slide preparation, and quality control checks.
  • Assist in generating feasibility, optimization, and analytical validation data for emerging CDx assays.
  • Manage tissue samples and associated documentation.
  • Prepare tissue sections, including slide cutting, baking, antigen retrieval, and reagent preparation.
  • Maintain sample integrity, traceability, and documentation in compliance with quality system requirements.
  • Support tissue handling workflows (blocks, slides, labeling, storage) within GLP or CLIA/CAP environments.
  • Accurately record experimental data in ELN and/or LIMS systems.
  • Capture high-quality slide images and perform basic image analysis.
  • Assist with slide scoring preparation and data summaries.
  • Summarize experimental findings for internal meetings and assay development reviews.
  • Operate, calibrate, and troubleshoot automated IHC staining platforms and related laboratory equipment.
  • Perform routine instrument maintenance and maintain equipment logs per laboratory quality systems.
  • Monitor and manage inventory of reagents, antibodies, controls, and consumables.
  • Collaborate with scientists, pathologists, QA, and clinical development teams on assay transfer, optimization, and validation activities.
  • Support preparation of study materials, controlled documents, and protocol execution for validation studies.

Benefits

  • 100% paid employee premiums for medical/dental/vision, also STD, LTD
  • a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years
  • 15 PTO days per year
  • sick leave
  • 11 paid holidays
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