Full-time · On-site

Director, Compliance

This is a high-impact leadership role designed for a compliance expert who thrives in the fast-paced environment of a biotech preparing for commercialization. You will be responsible for the end-to-end design of a global compliance program, ensuring ethical standards are met during critical therapy launches. It is a unique opportunity to transition from a purely advisory role to a strategic business partner in the rare disease space.

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Hiring company

Dyne Therapeutics

Waltham, Massachusetts, United Kingdom · Posted 26 April 2026

The role

Overview

This is a high-impact leadership role designed for a compliance expert who thrives in the fast-paced environment of a biotech preparing for commercialization. You will be responsible for the end-to-end design of a global compliance program, ensuring ethical standards are met during critical therapy launches. It is a unique opportunity to transition from a purely advisory role to a strategic business partner in the rare disease space.

The hiring side

About Dyne Therapeutics

Dyne Therapeutics is a mid-sized employer working in biotechnology, based in Waltham, Massachusetts, United Kingdom.

Industry

Biotechnology

Size

Medium

Location

Waltham, Massachusetts, United Kingdom

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What they need

Requirements & Skills

Key Responsibilities

  • Architect and execute a comprehensive healthcare compliance program
  • Develop and update corporate policies for Commercial, Medical, and Research divisions
  • Lead enterprise-wide risk assessments and mitigation strategies
  • Create and deliver specialized compliance training for all staff
  • Oversee internal investigations and ensure resolution of potential violations
  • Partner with Franchise Counsel to provide unified legal and compliance advice

Essential

  • Minimum of 10 years of total professional experience
  • At least 7 years of dedicated healthcare compliance experience
  • Deep expertise in U.S. healthcare laws and federal healthcare programs
  • Proven experience with therapy launches in the pharmaceutical sector
  • Strong understanding of the PhRMA Code
  • Experience in the biotechnology or pharmaceutical industry

Preferred

  • Prior experience specifically within global rare disease biotechnology companies
  • Advanced degree in Law (JD) or Business Administration (MBA)
  • Experience managing compliance for Value & Access and patient support programs

Key Skills

Strategic leadershipRisk assessment and prioritizationCross-functional collaborationInternal investigation managementCompliance training developmentAuditing and monitoring plan implementationKnowledge of FDA regulationsData privacy expertise

Networking

People to Know

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Perks

Benefits & perks

  • Opportunity to lead compliance for first-ever therapy launches
  • Collaborative and mission-driven work environment
  • Direct impact on patients with neuromuscular diseases
  • Strategic role within a growing biotechnology firm
  • Professional development in a high-growth sector

Next step

Apply now

Found via www.dyne-tx.com

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