Dyne Therapeutics
Healthcare & Life SciencesDirect Greenhouse career site

Director, QA GMP Operations

Pay
$188,000 – $230,000 per year
Location
Waltham, MA · On-site
Job type
Full-time
Level
Director
Experience
10+ years
Education
Bachelor's degree
Listed
31 days ago

Skills & highlights for this role

  • GMP quality operations
  • deviation and OOS investigation
  • batch record review
  • ICH guidelines

Also useful

  • IND/IMPD and BLA/MAA regulatory sections
  • tech transfer
  • process validation

Role Summary

The Director of QA GMP Operations is responsible for management of GMP quality within our external manufacturing operations globally and internal GMP operations for development and commercial programs. The Director will also work closely with internal business stakeholders as well as internal Quality function to deliver outcomes to advance programs within compliance. The Director is responsible for oversight of QA activities and ensuring the quality of deliverables within the role's purview.

This is an onsite role based in Waltham, MA.

Primary Responsibilities Include

  • Management of external quality operations in support of GMP manufacturing (clinical and commercial) activities.
  • Manage deviations, OOS and OOTs investigations while adhering to cGMP principles and ICH guidelines.
  • Review batch records, analytical method reports and technical reports including regulatory sections of IND/IMPD and BLA/MAAs.
  • QA support of Tech Transfer and Process Validation activities.
  • Disposition of GMP batches and interfacing with the Qualified Person (QP).
  • Change management to ensure proper evaluation of manufacturing and testing related changes by Quality, Regulatory, and Subject Matter Experts.
  • Manage CDMO performance within Quality Agreement expectations and GMP compliance.
  • Drive continuous improvement and inspection readiness.
  • Collaborate cross functionally to ensure pre-approval inspection and commercial readiness activities are completed at the CDMOs and internally.
  • Adjudicate on compliance discussions and negotiate any required corrective actions.
  • Create and foster a culture of collaboration and engagement for advancing quality outcomes and operational excellence.

Education and Skills Requirements

  • Minimum of a BA/BS degree
  • Minimum of 10+ years of experience in GMP Quality Operations in a clinical late stage and/or commercial biotechnology company
  • Leadership experience managing cross-functional teams with an ability to influence teams to prioritize activities and allocate resources without direct authority
  • Experience implementing and utilizing various outsourcing and support models
  • Experience with disposition of product batches and interfacing with a Qualified Person (QP)
  • Excellent written and oral communication skills, including well-developed presentation skills
  • Excellent organizational skills and ability to manage multiple priorities
  • Strong collaboration and interpersonal skills to effectively interact with internal or external stakeholders at all levels in the organization
  • General business management knowledge to assess the impact of project decisions on financial and corporate objectives
  • Ability to drive timelines, meet firm deadlines, and adapt quickly to changing requirements and priorities
  • Embrace Dyne's core values and culture

#LI-Onsite

Pay and benefits

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.

Company Overview

Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as preclinical programs for facioscapulohumeral muscular dystrophy (FSHD), Pompe disease and multiple DMD mutations. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities.

Read the original posting

From Dyne Therapeutics's careers page, first listed on Rolev.ai on October 10, 2026. Rolev.ai is not the employer.

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Common questions

What is the salary for the Director, QA GMP Operations role at Dyne Therapeutics?

The Director, QA GMP Operations posting at Dyne Therapeutics states compensation of $188,000 – $230,000 per year. It is listed as a full-time position. Final pay may depend on location, experience, and interview evaluation on Dyne Therapeutics's official career site.

Where is the Director, QA GMP Operations job at Dyne Therapeutics located?

This Director, QA GMP Operations position at Dyne Therapeutics is located in Waltham, MA (On-site). Always check Dyne Therapeutics's application page for specific state eligibility or relocation policies.

What qualifications are required for Director, QA GMP Operations at Dyne Therapeutics?

For the Director, QA GMP Operations role, Dyne Therapeutics highlights 10+ years of relevant experience; a bachelor's degree; experience with GMP quality operations, deviation and OOS investigation, batch record review, ICH guidelines. Rolev.ai can score your existing resume against these requirements and show any skill gaps before you apply.

How do I apply for the Director, QA GMP Operations position at Dyne Therapeutics?

This listing links directly to Dyne Therapeutics's Greenhouse application page. You can apply directly on Dyne Therapeutics's site, or use Rolev.ai to check your resume fit, generate a zero-hallucination tailored resume and cover letter for this posting, and autofill the Greenhouse application form in 1 click with the Rolev.ai Chrome extension. You always review the form and press Submit yourself.