Program Manager I

ATCCManassas, VA
$115,000 - $140,000Onsite

About The Position

A global nonprofit that provides trusted biological materials for science and health, ATCC is seeking a Program Manager I to lead complex, cross-functional programs onsite in Manassas, VA supporting regulated biological materials manufacturing and bioproduction. This role drives execution across multiple projects, ensuring alignment to quality systems, controlled documentation, and validated processes while delivering on schedule, budget, and performance commitments. The Program Manager is expected to demonstrate advanced communication skills and a strong command of project management fundamentals, with experience managing large-scale contracts (<$5M). The role requires the ability to effectively engage cross-functional teams and external stakeholders, including government customers, while ensuring program objectives are met within a highly regulated environment. Experience supporting projects regulated by ISO 13485 quality management systems is highly preferred, with a preference for candidates who bring a molecular biology foundation. Join ATCC and be part of a team that supports the global scientific community with trusted, authenticated biological materials.

Requirements

  • Bachelor’s degree and 8 or more years’ experience, including 0-2 years’ supervisory or equivalent experience.
  • Demonstrated ability to independently manage complex, multi-project programs with accountability for quality, compliance, and delivery outcomes.
  • Strong program management fundamentals, including planning, cost control, scheduling, and risk management.
  • Experience operating within regulated environments utilizing quality systems and controlled documentation.
  • Exceptional communication and stakeholder management skills across technical and business functions.
  • Ability to analyze metrics and drive continuous improvement.

Nice To Haves

  • Experience managing contracts exceeding $5M.
  • Knowledge of diagnostic kit manufacturing and ISO 13485 requirements, as well as molecular biology experience.
  • Experience working with government customers in regulated programs.

Responsibilities

  • Develops and executes integrated, cross-functional program plans across the full lifecycle, ensuring consistent delivery, risk management, and successful outcomes across multiple concurrent projects.
  • Oversees cost, schedules, and resource allocation; monitors technical performance and program metrics to ensure delivery within scope and budget.
  • Ensures all program activities comply with GMP principles, ISO-aligned quality systems, and controlled documentation requirements in regulated environments.
  • Serves as primary interface with sponsors, including government customers; communicates status, manages expectations, and supports growth and capture activities.
  • May hire, lead, and develop staff; drives accountability, coaching, and alignment to organizational goals.

Benefits

  • Comprehensive medical coverage
  • Company paid Life Insurance
  • Company paid Disability Insurance
  • Company paid AD&D
  • Paid parental leave
  • Paid Holidays
  • PTO
  • Fitness subsidies
  • Cell phone subsidies
  • Legal services
  • Pet insurance
  • Additional supplemental coverage
  • Employee Assistance Program
  • 401(a) (6% employer contribution) retirement plan
  • 403(b) (2% match) retirement plan
  • Corporate bonus program
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