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Director Global Quality Jobs (NOW HIRING)

Otsuka

Director, Global Product Quality - Manufacturing

$169K - $253K/yr

Position Summary The Director, Global Product Quality - Manufacturing Product Quality leads the quality oversight of clinical and commercial products at CDMOs under contract by Otsuka to ensure that ...

Itron, Inc

Director Quality

West Union, SC · On-site

Itron is seeking a Director, Global Manufacturing Quality. Reporting to the Vice President of Global Quality, this executive will lead operational execution and strategic alignment globally ...

Vrtx

Senior Director, Quality Systems/QMS

Boston, MA

The Senior Director, Global Quality Systems holds a pivotal leadership position within the Quality organization. This individual is responsible for providing strategic vision and direction to advance ...

Loparex LLC

Global Quality Manager

Cary, NC · On-site

$110 - $150/hr

Reporting to the Senior Director of Global Quality, this role provides tactical leadership for Loparex's global quality function, driving the execution and continuous improvement of our quality ...

Loparex LLC

Global Quality Manager

Cary, NC · On-site

Reporting to the Senior Director of Global Quality, this role provides tactical leadership for Loparex's global quality function, driving the execution and continuous improvement of our quality ...

Loparex LLC

Global Quality Manager

Cary, NC · On-site

Reporting to the Senior Director of Global Quality, this role provides tactical leadership for Loparex's global quality function, driving the execution and continuous improvement of our quality ...

Alkegen

Global Quality Manager

Buffalo, NY · On-site

$137K - $172K/yr

Global Quality Manager Alkegen brings together two of the world's leading specialty materials ... Provide direct line leadership to quality managers and quality engineers embedded in 12 ...

Probi

Quality Manager

Lafayette, CO

Under the guidance of the Sr Director Global Quality, the Quality Manager is responsible for assessing the current and establishing an improved and effective Quality Management System to ensure the ...

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$213.5K

How much do director global quality jobs pay per year?

As of Aug 18, 2026, the average yearly pay for director global quality in the United States is $125,600.00, according to ZipRecruiter salary data. Most workers in this role earn between $91,000.00 and $151,000.00 per year, depending on experience, location, and employer.

What is a director global quality?

A Director of Global Quality is responsible for overseeing and ensuring product or service quality across multiple regions or markets. They develop and implement quality assurance strategies, compliance programs, and continuous improvement initiatives to meet industry and regulatory standards. This role often involves collaborating with cross-functional teams, managing audits, and driving global consistency in quality management. Strong leadership, strategic planning, and expertise in quality systems are essential skills for success in this role.

What are the key skills and qualifications needed to thrive in the director global quality position?

To thrive as a Director Global Quality, you need extensive experience in quality management systems, regulatory compliance, and process improvement, usually complemented by a degree in a scientific or engineering discipline. Proficiency with international quality standards (such as ISO 9001), audit management software, and certifications like Six Sigma or ASQ Certified Quality Engineer is often required. Strong leadership, cross-cultural communication, and strategic problem-solving skills help you effectively manage global teams and drive continuous improvement initiatives. These competencies ensure consistent product quality, regulatory adherence, and operational excellence across all regions in a global organization.

What are typical challenges a director global quality might face in a multinational organization?

A Director Global Quality often navigates challenges such as aligning quality standards across diverse regions, ensuring compliance with varying international regulations, and managing culturally different teams. Adapting quality processes to meet both corporate expectations and local requirements can require creative problem-solving and strong change management skills. Additionally, maintaining clear communication channels between headquarters and regional offices is crucial for the consistent implementation of quality initiatives. Overcoming these challenges provides valuable experience and significant impact on an organization's global reputation and operational success.

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Director Global Quality jobs near you
Infographic showing various Director Global Quality job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $125,600 per year, or $60.4 per hour.

Sr. Director, Global Quality Control

Scholar Rock

Cambridge, MA • On-site

$245K - $305K/yr

Full-time

Re-posted 19 days ago

Job description

Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.
Summary of Position:
Position Responsibilities
  • Lead the company's global QC function across a fully outsourced model, with end-to-end oversight of external QC laboratories, CMOs, and contract partners supporting clinical and commercial programs.
  • Define and execute the global QC strategy, serving as the internal QC subject matter expert across analytical control strategy, compendial compliance, specification lifecycle management, and stability.
  • Provide strategic oversight of stability programs, including protocol design, pull schedule governance, data review and trending, shelf-life support, comparability assessments, and post-approval stability commitments.
  • Oversee post-approval specification management, including revision strategy, change assessment, comparability impacts, commitment tracking, and implementation through external partners.
  • Ensure effective method qualification, validation, transfer, verification, and lifecycle management across outsourced laboratories, including technical troubleshooting and issue escalation.
  • Partner with Analytical Development and CMC teams to support method readiness, control strategy development, and phase-appropriate analytical plans for new programs, process changes, and commercialization activities.
  • Provide QC leadership for investigations involving OOS, OOT, non-conforming results.
  • Establish and monitor quality and operational performance expectations for external testing partners through governance forums, metrics, trend reviews, and business process oversight.
  • Author, review, and approve QC-related controlled documents, including specifications, protocols, reports, SOPs, method transfer plans, stability documents, and technical assessments as applicable.
  • Build fit-for-purpose QC systems, governance, and internal capabilities appropriate for a virtual biotech environment, with a focus on compliance, technical rigor, and scalability.
  • Collaborate with the Head of Quality and site leadership to ensure alignment with corporate goals, customer expectations, and regulatory obligations (FDA, EU, and other global regulators).

Candidate Requirements
  • BS/MS degree in a scientific discipline; advanced degree (MS or PhD) preferred
  • 15+ years of progressive Quality Control and/or Analytical Sciences experience in biotech/pharma industry (including outsourced operating models), with 7+ years in leadership roles
  • Deep technical expertise in analytical methods supporting biologics and/or other advanced therapeutic modalities, including release, stability, and characterization testing.
  • Strong working knowledge of USP, EP, and JP pharmacopeial requirements, and cGMP, ICH guidance, global regulatory requirements, and inspection readiness for outsourced QC operations.
  • Demonstrated success leading global stability programs, including shelf-life support, data trending, protocol governance, and regulatory commitment execution.
  • Proven experience in specification development, justification, and lifecycle management, including post-approval specification revisions and change implementation.
  • Extensive experience with method transfer, qualification, validation, verification, and troubleshooting across contract testing laboratories and manufacturing partners.
  • Proven ability to lead through influence in a matrixed organization and manage complex external technical relationships with appropriate rigor and accountability.
  • Strong executive presence, sound scientific judgment, and the ability to balance strategic leadership with practical execution.
  • Highly proactive, decisive, and capable of independently managing key initiatives.
  • Engaged people manager committed to building culture as well as mentorship and talent development

$245,000 - $305,000 a year
Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

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