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Executive Director, QMS & Digital

Job in Waltham, Middlesex County, Massachusetts, 02254, USA
Listing for: Scorpion Therapeutics
Full Time position
Listed on 2026-09-12
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 240000 - 360000 USD Yearly USD 240000.00 360000.00 YEAR
Job Description & How to Apply Below

Position Summary

  • Own and be accountable for the strategy, governance, effectiveness, compliance, and continuous improvement of the Company’s Quality Management System (QMS), ensuring it operates as an integrated, reliable, and scalable system.
  • Serve as enterprise Quality owner for QMS governance, processes, and frameworks for document control and training, CAPA, change control, quality events and deviations, and process excellence.
  • Own digital and data capabilities enabling a modern QMS, including Quality digital and AI strategy, Quality metrics and data infrastructure, and computerized system validation (CSV). Lead/develop teams and partner across the organization.
Responsibilities
  • Own overall QMS performance: compliance, effectiveness, reliability, inspection readiness, continuous improvement.
  • Lead core QMS processes: document control/training, CAPA, change control, quality events/deviations.
  • Establish governance and performance management using risk, metrics, trends, and management review.
  • Lead Quality Process Excellence to simplify/standardize/optimize processes while maintaining compliance.
  • Develop and execute Quality digital strategy/roadmap and automation (with IT and stakeholders).
  • Own Quality metrics and data infrastructure to enable actionable insights and proactive management.
  • Provide oversight for CSV, data integrity, and compliant lifecycle management of Quality systems.
  • Lead and develop a high-performing team; serve as senior Quality partner for inspections, audits, and external assessments.
Qualifications
  • Bachelor’s degree (advanced degree preferred). 15+ years Quality experience in life sciences; 8+ years GMP experience.
  • Deep QMS strategy/governance expertise and core QMS processes (document management, training, CAPA, change control, deviations/quality events, investigations, management oversight).
  • Knowledge of global GxP; experience maintaining inspection-ready QMS and supporting/leading inspections and audits.
  • Experience in Quality process excellence, digital transformation, Quality data/analytics, regulated technology environments (CSV, data integrity).
  • Understanding of responsible AI use in regulated environments (governance, risk, validation, compliance).
  • Proven leadership and ability to influence stakeholders and translate strategy into measurable execution.
  • Strong systems thinking, judgment, communication, and change leadership; ability to balance compliance, risk, operational effectiveness, technology, and business needs.
  • Travel up to 20%.
Benefits
  • 401(k) with generous employer match; 12 weeks paid parental leave; up to 12 weeks living organ and bone marrow leave; equity incentive plans; medical/prescription/dental/vision; life insurance and disability; flexible time off;
    Winter Holiday shutdown; at least 11 paid holidays.
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