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Remote Director Global Quality Jobs (NOW HIRING)

Harbor

Director, Global Compliance

Harbor is seeking a Director of Global Compliance to establish, lead, and continuously evolve the ... This is a remote position that can be worked from anywhere in the USA (EST/CST preferred). Key ...

LabConnect

Director, Quality Operations

Johnson City, TN · On-site +1

We are an independent, global, one-stop-shop focused on delivering Central Laboratory Services that ... The Director, Quality Operations for the US provides strategic leadership and oversight of quality ...

Samsara

Director, Global Service Partnerships

$132K - $236K/yr

... quality partner programs that support customer deployments and long-term success. This team ... This is a remote position open to candidates residing in the US except the San Francisco Bay Metro ...

Amgen, Inc.

Director, Global Content Production

Director, Global Content Production What you will do Let's do this. Let's change the world. In this ... The role is accountable for production quality, speed, compliance, cost efficiency, partner ...

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$31K

$125.6K

$213.5K

How much do remote director global quality jobs pay per year?

As of Aug 14, 2026, the average yearly pay for remote 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 the difference between Remote Director Global Quality vs Remote Quality Manager?

AspectRemote Director Global QualityRemote Quality Manager
CredentialsTypically requires advanced degrees (e.g., Bachelor's or Master's in Quality, Engineering, or related fields) and extensive experienceUsually requires a Bachelor's degree in Quality, Engineering, or related fields with relevant experience
Work EnvironmentOversees global quality strategies, collaborates with multiple departments, and manages international teams remotelyManages quality processes within specific departments or regions, often coordinating with teams remotely
Employer & Industry UsageCommon in multinational corporations across manufacturing, healthcare, and technology sectorsUsed in various industries for regional or departmental quality oversight

The Remote Director Global Quality focuses on strategic, high-level oversight of global quality initiatives, requiring extensive experience and advanced credentials. In contrast, the Remote Quality Manager handles day-to-day quality operations within specific areas, often with less seniority. Both roles are vital in maintaining quality standards but differ mainly in scope and responsibility.

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Remote Director Global Quality jobs near you
Infographic showing various Remote Director Global Quality job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $125,600 per year, or $60.4 per hour.

Associate Director - Corporate Quality Compliance (QMS)

Zimmer, Inc.

Remote

$130K - $165K/yr

Full-time

Posted 16 days ago

Job description

Zimmer Biomet is a global medical technology leader. Our team members are part of a company with a heritage of leadership, a focus on shaping the future, and a mission dedicated to alleviating pain and improving the quality of life for people around the world.


What You Can Expect


This position serves as the organization's subject matter expert on global Quality Management System compliance, providing authoritative knowledge and strategic direction across the full scope of applicable regulations, standards, and international frameworks. This position also leads a team of quality professionals who define, implement, and monitor the global QMS at Zimmer Biomet.

How You'll Create Impact
  • Architect and drive the global Quality Management System strategy, including systemic CAPA programs, quality system enhancements, and cross-functional improvement initiatives that strengthen compliance and operational performance across all manufacturing sites, design centers, and distribution centers.
  • Direct the development, harmonization, and continuous improvement of corporate quality policies, procedures, and processes to ensure sustained compliance with applicable global regulations, standards, and evolving regulatory expectations.
  • Interface with external regulatory bodies - lead strategy for FDA inspections, notified body audits, and other regulatory engagements across the global network, consult on agency communications, and post-inspection commitments.
  • Lead quality due diligence for mergers and acquisitions, designing and executing integration strategies that bring newly acquired entities into full alignment with the Zimmer Biomet Quality Management System.
  • Represent Zimmer Biomet in a leadership capacity within key industry bodies (e.g., AdvaMed, AAMI), translating emerging standards, regulatory trends, and industry best practices into actionable updates to corporate quality policies and procedures.
  • Own and lead the Corporate Management Review and Global Quality Report process end-to-end - through executive presentation and tracking of resulting actions to closure.
What Makes You Stand Out
  • Demonstrated knowledge and experience in interpreting and applying regulations and standards for Quality Management Systems that govern design, manufacturing and distribution of products worldwide including but not limited to FDA 21 CFR Part 820 (QMSR), ISO 13485:2016, EU MDR (EU) 2017/745, Canadian Medical Devices Regulations (SOR/98-282), Japan's Pharmaceuticals and Medical Devices Act (PMD Act) and MHLW Ministerial Ordinance No. 169, MDSAP
  • Acts in a balanced and ethical manner when dealing in gray areas of regulation.
  • Utilizes leadership and motivational skills sufficient to manage multiple projects and interface with personnel from varied backgrounds and cultures in local and remote locations across all company disciplines and business units.
  • Excellent interpersonal skills - Builds and maintains relationships inside and outside the organization.
  • Exhibits good business sense, makes sound and timely scientific and business decisions.
  • Able to advocate positions in the face of adversity.
  • Excellent oral, writing, and presentation skills.
  • Excellent analytical and problem solving skills.
  • Computer literacy including Microsoft Office Suite.
Your Background
  • Bachelor's degree in life sciences, technical discipline, or business is required. (Master's degree is preferred).
  • 7-10 years of experience in a quality, regulatory or quality compliance role is required. Experience with establishing and/or maintaining quality management systems in a medical device manufacturing organization is strongly preferred.
  • Medical Device regulations knowledge and experience required.
  • FDA or Notified Body experience required.
  • Audit or ASQ certifications such as RABQSA, CQA, CQE are strongly preferred.
Travel Expectations
  • Up to 20%


Expected compensation: $130,000 - $165,000 base salary. Comprehensive bonus also provided.


EOE

Employment Type: OTHER

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