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Global Quality Operations Jobs (NOW HIRING)

10x Genomics

SR Director Global Quality

Pleasanton, CA · On-site

Senior Director, Global Quality Assurance About the Role 10x Genomics is seeking an accomplished ... This individual will partner across Operations, R&D, and Commercial teams to design and implement ...

TERUMO BCT, INC

Collaborating closely with R&D, Operations, Commercial teams, Regulatory Affairs, and Quality ... Lead the global Quality Assurance organization to develop, implement, govern, and continuously ...

IDEX

Director, Global Quality - PneumaticsSkip to main contentWe use cookies to ensure that we give you ... With interesting opportunities in engineering, marketing, sales, supply chain, operations, HR ...

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Global Quality Operations information

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How much do global quality operations jobs pay per year?

As of Sep 15, 2026, the average yearly pay for global quality operations in the United States is $91,047.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,500.00 and $110,000.00 per year, depending on experience, location, and employer.

What is global quality operations?

Global Quality Operations refer to the oversight and management of quality systems and processes across all locations and manufacturing sites of a global organization. This function ensures that products and services meet regulatory requirements and company standards no matter where they are produced or distributed. Teams in Global Quality Operations develop and enforce quality policies, conduct audits, manage compliance, and drive continuous improvement initiatives. Their work is critical in industries like pharmaceuticals, manufacturing, and food, where consistent quality and safety are essential worldwide.

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

To excel in Global Quality Operations, you need a solid background in quality assurance, regulatory compliance, and process improvement, usually supported by a degree in life sciences, engineering, or a related field. Familiarity with quality management systems (QMS), global regulatory standards (such as ISO 9001 or GMP), and relevant certifications like Six Sigma or ASQ is highly valued. Strong analytical thinking, cross-cultural communication, and leadership skills help professionals navigate complex global environments and collaborate across teams. These competencies are crucial for ensuring consistent product quality, regulatory adherence, and operational efficiency on an international scale.

How does the global quality operations team typically collaborate with other departments to ensure compliance and product quality across international sites?

Global Quality Operations professionals work closely with cross-functional teams such as manufacturing, supply chain, regulatory affairs, and R&D to ensure consistent quality standards and regulatory compliance worldwide. Regular communication is essential, often involving virtual meetings across time zones, shared documentation platforms, and coordinated audits or inspections. This collaborative approach helps to align quality objectives, swiftly address any issues, and implement best practices across all sites, making teamwork and strong communication skills key aspects of the role.

What is the difference between Global Quality Operations vs Quality Assurance Specialist?

AspectGlobal Quality OperationsQuality Assurance Specialist
Primary FocusOversees quality management across multiple regions and ensures global complianceFocuses on product quality testing and process validation within specific projects or departments
CertificationsISO 9001, Six Sigma, GMP often requiredISO 9001, Six Sigma, GMP often required
Work EnvironmentGlobal offices, manufacturing sites, cross-functional teamsLaboratories, production lines, quality departments
Industry UsageCommon in manufacturing, pharmaceuticals, biotechCommon in manufacturing, pharmaceuticals, biotech

Global Quality Operations roles involve managing quality standards across multiple regions, ensuring compliance, and coordinating global quality initiatives. In contrast, Quality Assurance Specialists focus on testing, validation, and ensuring product quality within specific areas. Both roles often require similar certifications and work in related environments, but their scope and responsibilities differ significantly.

What is a global quality operations job?

A global quality operations job involves managing and ensuring quality standards across multiple regions or countries within an organization. It includes tasks such as overseeing quality control processes, implementing compliance protocols, and coordinating with international teams to maintain product or service quality. Strong analytical skills, knowledge of industry regulations, and familiarity with quality management tools are often required.
More about Global Quality Operations jobs

What are popular job titles for Global Quality Operations?

Popular job titles for Global Quality Operations:

Global Quality Operations jobs near you
Infographic showing various Global Quality Operations job openings in the United States as of September 2026, with employment types broken down into 2% As Needed, 80% Full Time, 14% Part Time, 3% Contract, and 1% Nights. Highlights an 83% Physical, 1% Hybrid, and 16% Remote job distribution, with an average salary of $91,047 per year, or $43.8 per hour.

Director, Global Quality & Compliance

Lakewood, CO • On-site

Terumo BCT, Inc.
Manufacturing • 1 - 5K employees
Learn more about Terumo BCT, Inc.external

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 27 days ago

Job description

Requisition ID: 35415
At Terumo Blood and Cell Technologies, our 8,000+ global associates proud to come to work each day, knowing that what we do impacts the lives of patients around the world. For Terumo, for Everyone, Everywhere.
We make medical devices and related products that are used to collect, separate, manufacture and process various components of blood and cells. With our innovative technologies and service offerings, we touch a patient's life every second of every day and are committed to continuing to increase the number of patients we serve. Advancing healthcare with heart.
With some of the best and brightest minds in the industry, an unmatched global footprint, comprehensive benefits and a distinct culture, Terumo Blood and Cell Technologies is a great place to work, grow and be part of a team that is focused on making a difference. Join us and help shape wherever we go next. You create your future and ours.
The Director, Global Quality & Compliance is responsible for developing, implementing, maintaining, and continuously improving global quality management systems, standards, and governance across all areas of quality. This role ensures global quality processes are effective, harmonized, scalable, and compliant with applicable regulatory requirements, international standards, and industry best practices. The position provides strategic leadership for global quality assurance, regulatory compliance, inspection readiness, validation, laboratory controls, post-market compliance, and continuous improvement initiatives that support customer, patient, and regulatory expectations. This leader also drives adoption of digital transformation efforts that strengthen quality system performance, data integrity, compliance oversight, and operational efficiency. Collaborating closely with R&D, Operations, Commercial teams, Regulatory Affairs, and Quality functions, this leader oversees critical projects in alignment with key business initiatives. This role reports directly to the VP of Global Quality.
ESSENTIAL DUTIES
Quality Assurance
  • Lead the global Quality Assurance organization to develop, implement, govern, and continuously improve global quality management systems and standards across all areas of quality management in compliance with FDA QMSR, ISO 13485, EU MDR, and other applicable international requirements.
  • Maintain accountability for the design, implementation, effectiveness, harmonization, and continuous improvement of core global quality processes, including document control, nonconformance, CAPA, internal audit, management review, validation, laboratory controls, post-market compliance, and other globally standardized quality system processes.
  • Drive adoption of digital transformation initiatives within the global quality organization, including validated digital systems, quality data analytics, automation, and standardized tools that improve compliance oversight, process efficiency, visibility, and evidence-based decision-making.
  • Provide leadership and oversight for post-market compliance, including complaint handling, adverse event reporting, medical safety evaluations, post-market surveillance, quality signal escalation, field action support, and implementation of related process improvements.
  • Provide leadership and oversight of global validation activities, including validation strategy, risk assessments, protocol development, execution oversight, cross-functional alignment for business-critical initiatives, and implementation of related process improvements.
  • Provide leadership and oversight of global internal audit and inspection readiness activities, including oversight of internal and due diligence audits, timely resolution of audit findings, preparation for regulatory inspections, maintenance of applicable notified body and quality system certifications, and implementation of related process improvements.

Regulatory Compliance
  • Ensure global quality processes remain aligned with applicable regulatory requirements, including FDA, EMA, ISO, and country-specific standards.
  • Proactively monitor regulatory and industry changes and implement updates to global quality policies, procedures, standards, and governance practices.
  • Represent the company during regulatory inspections and audits, achieving favorable outcomes and resolving findings efficiently.

Leadership and Strategy
  • Define and execute a global quality and compliance strategy that strengthens quality system maturity, supports business goals, enables digital transformation, and promotes consistent execution across regions and functions.
  • Build and inspire high-performing quality teams across regions, fostering a culture of excellence and compliance.
  • Partner with cross-functional teams (e.g., R&D, manufacturing, supply chain, clinical) to ensure quality is integrated throughout the product lifecycle.
  • Participates as a member of the Quality Leadership team.

Risk Management and Continuous Improvement
  • Identify and mitigate quality and compliance risks through proactive monitoring and intervention.
  • Drive a culture of continuous improvement by implementing quality metrics, analyzing performance trends, using digital and data-enabled insights, and leading initiatives that optimize quality system effectiveness and process performance.
  • Lead root cause investigations for quality issues and implement corrective and preventive actions.

MINIMUM QUALIFICATION REQUIREMENTS
Education
  • Bachelor's degree in engineering, life sciences, or a related field required; advanced degree such as MS, MBA, or PhD strongly preferred.
  • Minimum 10 years of progressive experience in quality assurance, quality systems, manufacturing, or regulatory compliance within a regulated industry, such as medical devices, pharmaceuticals, biotechnology, or combination products.
  • Strong knowledge of international regulatory requirements, including FDA QMSR, ISO 13485, EU MDR/IVDR, and applicable country-specific regulations as applicable to medical devices, drug manufacturing and/or combination products.
  • Demonstrated experience supporting regulatory inspections, audits, certifications, and related inspection readiness activities.
  • Demonstrated leadership experience managing global teams and complex quality initiatives.
  • Six Sigma Black Belt or Master Black Belt certification preferred.

Skills
  • Exceptional analytical, problem-solving, and decision-making skills, particularly in high-pressure environments.
  • Outstanding interpersonal and communication skills, with the ability to engage effectively with cross-functional stakeholders and external regulators.
  • Expertise in quality management software, tools, and data analytics to support decision-making.
  • Demonstrated knowledge of manufacturing operations, process and computer systems validation, engineering, tactical execution, customer service, professional communications, cross-functional collaboration, computer applications, problem solving, strategic reasoning, teamwork, change management, business acumen, and business ethics.
  • Demonstrated expertise in planning, budgeting, and project management toward achievement of annual, long-term, and strategic business objectives.

-Or-
An equivalent competency level acquired through a variation of these qualifications may be considered.
LOCATION
Lakewood, Colorado - Onsite (hybrid)
TRAVEL
  • There will be an occasional requirement to work outside of normal business hours, consistent with other manufacturing positions.
  • U.S. and international travel may be required up to 40%.

PHYSICAL REQUIREMENTS
  • Typical office environment requirements include reading, speaking, hearing, close vision, traversing, bending, sitting, and occasional lifting up to 20 pounds.
  • The physical demands described here are representative of those that must be met by an associate to successfully perform the essential duties of this job.
  • Reasonable accommodations may be made to enable individuals with disabilities to perform the essential duties.

Target Pay Range: $199,600.00 to $249,500.00 - Salary to be determined by the education, experience, knowledge, skills, and abilities of the applicant, internal equity, and alignment with market data
Target Bonus on Base: 30.0%
We anticipate this requisition will be open for a minimum of five (5) days, from August 19, 2026. We encourage your prompt application.
At Terumo Blood and Cell Technologies, we provide competitive total reward offerings that consist of compensation, benefits, recognition, along with a wealth of other well-being, work-life and recognition programs which support in unlocking the potential for you and your family. Included in our expansive list of benefits offerings are multiple group medical, dental and vision plans, a robust wellness program, life insurance and disability coverages, also a variety of voluntary programs such as group accident, hospital indemnity, critical illness, pet insurance and much more. To help you save for retirement, we offer a 401(k) plan with a matching contribution and for work-life balance we have vacation and sick time programs for associates. For us, it's about protecting the personal welfare of our associates and their families, helping to achieve personal goals and offering those extra touches for convenience, security and overall peace of mind.
  • Terumo Blood and Cell Technologies is part of Terumo Group, founded in 1921 and headquartered in Tokyo, Japan.
  • In 2024, Terumo Blood and Cell Technologies reached $1.5 billion in revenue.
  • We employ nearly 8,000 associates globally, with global headquarters in Lakewood, CO, U.S., and regional headquarters in Brussels, Buenos Aires, Singapore and Tokyo.
  • We manufacture devices, disposable sets and solutions at our facilities in Belgium, India, Japan, Northern Ireland, the U.S. and Vietnam. Our global presence enables us to serve customers in more than 130 countries.
  • Our core values help set our direction, guide our actions and keep us true to our corporate mission of contributing to society through healthcare.
    • Respect - Appreciative of others
    • Integrity - Guided by our mission
    • Care - Empathetic to patients
    • Quality - Committed to excellence
    • Creativity - Striving for innovation
  • We contribute to the Leukemia and Lymphoma Society (LLS), raising $2.4 million USD since 2025.

We are proud to be an Equal Opportunity Affirmative Action Employer. All applicants will be afforded equal opportunity without discrimination because of race, color, religion, sex, gender identity or expression, sexual orientation, marital status, order of protection status, national origin or ancestry, citizenship status, age, physical or mental disability unrelated to ability, military status or an unfavorable discharge from military service.
Terumo Blood and Cell Technologies is committed to providing a safe, healthy and secure working environment. Our Colorado campus locations are tobacco-free workplaces, and we maintain a drug-free workplace and perform pre-employment substance abuse testing and detailed background verification.

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