Dyne Therapeutics

Director, Quality Management Systems

Dyne Therapeutics$196K — $230K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in a scientific discipline or Quality Systems Management; advanced degree preferred
  • 10+ years of experience in biotechnology or pharmaceutical environments with GxP exposure (GCP, GLP, GMP, GVP preferred)
  • Experience with direct ownership of Quality Management Systems (QMS)
  • In-depth understanding of global regulatory requirements (FDA CFRs, ICH guidance, EU Annex)
  • Proven experience with eQMS platforms like Veeva or MasterControl
  • Strong strategic and operational capabilities
  • Exceptional communication skills to influence senior stakeholders

Responsibilities

  • Lead the evolution of a globally scalable QMS aligned with international standards
  • Ensure QMS processes are phase-appropriate and risk-based
  • Establish a proactive compliance model for continuous inspection readiness
  • Serve as the QMS expert during regulatory inspections
  • Oversee a risk-based internal audit program across functions
  • Identify systemic quality risks and ensure effective CAPA processes
  • Drive continuous improvement initiatives for QMS efficiency

Benefits

  • Flexible working arrangements and a hybrid work environment
  • Professional development opportunities and tuition reimbursement
  • Comprehensive health and wellness programs
  • Paid time off and holidays
  • 401(k) plan with company match
Full Job Description
Role Summary:

The Director, Quality Management Systems is a quality leader responsible for designing, scaling, and advancing a global Quality Management System (QMS) that supports Dyne's transition to commercial operations. This role is responsible for key elements of the QMS including supplier quality, audits, and product complaint management programs, ensuring these systems are inspection-ready, risk-based, and aligned with global regulatory expectations. The Director will partner cross-functionally to embed quality as a strategic enabler of business performance, ensuring systems are fit-for-purpose, inspection-ready, scalable, and efficient as the organization grows. This is a hands-on leadership role that requires both strategic vision and operational execution.

This role is based in Waltham, MA.

Primary Responsibilities Include:

QMS Strategy, Compliance & Inspection Readiness
  • Leads the evolution of the QMS into a commercial-ready, globally scalable system aligned with ICH Q10, FDA CFRs, and international regulatory standards
  • Ensures QMS processes are phase-appropriate, risk-based, and designed to scale with organizational growth
  • Establishes and sustains a proactive compliance model that supports continuous inspection readiness
  • Serves as a subject matter expert and primary representative for assigned QMS areas during regulatory inspections and health authority interactions

Core QMS Program Ownership
  • Leads a risk-based internal audit program, including planning, execution, and follow-up across functions
  • Identifies systemic quality risks and ensures timely CAPA development, closure, and effectiveness checks
  • Builds and matures a risk-based supplier quality program, including supplier qualification, monitoring, and ongoing oversight
  • Oversees the end-to-end product complaint management lifecycle, including intake, triage, investigation, escalation, and trending, ensuring scalability for commercial distribution

Operational Excellence & Systems Enablement
  • Defines, monitors, and reports quality metrics and KPIs to assess system health, compliance risk, and performance trends
  • Drives continuous improvement initiatives to enhance efficiency, reduce risk, and strengthen QMS robustness
  • Leads the implementation, optimization, and governance of eQMS platforms, ensuring validated systems, strong user adoption, and effective lifecycle management

Cross-Functional Leadership & Quality Culture
  • Partners with cross-functional stakeholders to embed quality into business processes and decision-making
  • Communicates quality risks, dependencies, and tradeoffs with clarity and urgency, influencing outcomes without direct authority
  • Contributes to building a high-performing quality organization and models a culture of accountability, transparency, and continuous improvement

Education and Skills Requirements:
  • Bachelor's degree in a scientific discipline or Quality Systems Management; advanced degree preferred
  • 10+ years of experience in biotechnology or pharmaceutical environments, with exposure across GxPs (GCP, GLP, GMP, GVP preferred)
  • Demonstrated leadership experience with direct ownership of QMS and quality systems
  • Deep understanding of global regulatory requirements, including FDA CFRs, ICH guidance, and EU Annex requirements
  • Proven experience implementing and managing eQMS platforms (e.g., Veeva eQMS, MasterControl) and Learning Management Systems
  • Strong strategic and operational capability, balancing vision-setting with hands-on execution
  • Proven ability to manage multiple complex initiatives in a fast-paced, dynamic environment
  • Strong judgment and risk management skills, balancing compliance, science, and business needs
  • Exceptional written and verbal communication skills with the ability to influence senior and cross-functional stakeholders
  • Highly proactive, accountable, and comfortable operating with a high degree of autonomy

#LI-Onsite

MA Pay Range

$196,000-$230,000 USD

The pay range reflects the base pay range Dyne reasonably expects to pay for this role at the time of posting. Individual compensation depends on factors such as education, experience, job-related knowledge, and demonstrated skills.

The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements. Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.

About Dyne Therapeutics

Dyne Therapeutics is a biotechnology company that is focused on developing therapies for patients with genetically driven muscle diseases. The company is developing a platform that is designed to deliver nucleic acids to muscle tissue. Dyne's lead product candidate is DYN101, which is a treatment for patients with myotonic dystrophy type 1 (DM1). DM1 is a genetic disorder that affects the muscles and other body systems. DYN101 is designed to reduce the levels of toxic RNA that are produced by the mutated gene that causes DM1. The company was founded in 2018 and is headquartered in Cambridge, Massachusetts.
Learn more about Dyne Therapeutics
Size
70 employees
Market Cap
$633.4 million
Industry
NASDAQ

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