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Senior Scientist — Advanced Human Model Systems

Job in Baltimore, Anne Arundel County, Maryland, 21276, USA
Listing for: Blackbird Laboratories
Full Time position
Listed on 2026-08-09
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist
  • Research/Development
    Biotech Research, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 145000 - 175000 USD Yearly USD 145000.00 175000.00 YEAR
Job Description & How to Apply Below

Position: 12-month contract, with potential to convert to a permanent role;
On-site, Baltimore, MD

Anticipated start date: September 1, 2026

Expected salary range: $145,000–$175,000, commensurate with experience

ABOUT NCAC

The National Center to Accelerate Cures (NCAC) is an independent nonprofit institute dedicated to accelerating the regulatory acceptance and commercial adoption of New Approach Methodologies (NAMs). NCAC works with technology developers, regulators, industry and academic partners to generate the evidence needed to validate promising NAMs for regulatory decision-making. In its first year, NCAC will validate its first NAMs, establish shared standards for the field, and build the data infrastructure needed to support regulatory review at scale.

POSITION

SUMMARY

Serve as NCAC's technical expert in advanced human biological model systems, ensuring externally developed NAMs can be robustly implemented, standardized and operated within NCAC validation workflows.

KEY RESPONSIBILITIES
  • Implement organoids, organ-on-chip and other advanced models from external developers.
  • Establish reproducible in-house workflows while preserving developer methodologies.
  • Troubleshoot diverse model systems.
  • Benchmark model performance.
  • Develop SOPs and train staff.
REQUIRED QUALIFICATIONS
  • PhD with typically 4+ years relevant experience.
  • Hands-on experience across multiple advanced model systems.
  • Experience implementing technologies from external collaborators.
  • Strong troubleshooting skills.
PREFERRED QUALIFICATIONS
  • Quality systems and documentation.
  • Workflow standardization.
  • Commercial platform experience.
COMMITMENT TO SCIENTIFIC QUALITY & REGULATORY RIGOR

Successful candidates will have experience working within structured scientific environments where reproducibility, standardized workflows, traceability, data integrity, and documentation are essential. Experience with SOP development, GLP/GCLP/GMP or comparable quality systems, validation studies, and audit-ready documentation is highly valued.

WHAT YOU'LL ACCOMPLISH IN YOUR FIRST 60 DAYS

As NCAC establishes its laboratory infrastructure, you will lead implementation of the institute's advanced biological model capabilities.

  • Assist with laboratory design, equipment selection, and setup to support advanced human in vitro model systems.
  • Establish standardized workflows for cell culture, organoid, and organ-on-chip systems expected to support NCAC's first validation studies.
  • Work closely with NAM developers to understand technical requirements and ensure successful implementation of externally developed model systems.
  • Develop laboratory SOPs for culture, maintenance, operation, and quality control of advanced biological models.
  • Lead procurement of biological materials, culture reagents, consumables, and model-specific supplies.
  • Execute initial culture optimization and control experiments to establish robust, reproducible laboratory workflows.
SUCCESS IN THE FIRST 12 MONTHS
  • Establish multiple external NAM platforms.
  • Become NCAC's technical implementation expert.
  • Standardize workflows and training.
  • Support reproducible validation studies.
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Position Requirements
10+ Years work experience
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