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Global Quality Operations Jobs (NOW HIRING)

kindeva

Sr. Director, Quality Operations

Bridgeton, MO · On-site

Represent the site in global quality governance to ensure harmonization of systems and processes ... Ensure site operations comply with FDA, EMA, ICH, ISO 13485, and other global requirements. * Serve ...

General Motors

Quality Manager

Lansing, MI · On-site

Collaborating closely with Shop Directors and cross-functional manufacturing teams, you will define, approve, and standardize Global Quality Operations requirements, launch quality system procedures ...

kindeva

Sr. Director, Quality Operations

Bridgeton, MO · On-site

Represent the site in global quality governance to ensure harmonization of systems and processes ... Ensure site operations comply with FDA, EMA, ICH, ISO 13485, and other global requirements. * Serve ...

kindeva

Sr. Director, Quality Operations

Bridgeton, MO · On-site

Represent the site in global quality governance to ensure harmonization of systems and processes ... Ensure site operations comply with FDA, EMA, ICH, ISO 13485, and other global requirements. * Serve ...

Agropur

Senior Manager Quality Operations

Appleton, WI · On-site

$155 - $300/hr

Operations) and provides technical and quality leadership to support the deployment, monitoring ... Lead assigned projects to implement new programs (i.e. global quality roadmap), improve quality ...

Agropur

Senior Manager Quality Operations

Appleton, WI · On-site

$155 - $300/hr

Operations) and provides technical and quality leadership to support the deployment, monitoring ... Lead assigned projects to implement new programs (i.e. global quality roadmap), improve quality ...

Agropur

Senior Manager Quality Operations

Le Sueur, MN · On-site

$155 - $300/hr

Operations) and provides technical and quality leadership to support the deployment, monitoring ... Lead assigned projects to implement new programs (i.e. global quality roadmap), improve quality ...

victaulic

Global Quality & Compliance Manager

You'll partner closely with Operations, Global Quality, Procurement, and plant leadership to ensure products meet global standards, corrective actions stick, and compliance isn't just a policy - it ...

Masimo

Sr Director, Quality

Irvine, CA · On-site

Assess quality risks across global sites and operations, identifying opportunities to strengthen compliance, improve processes, and mitigate enterprise risk. * Monitor emerging global regulatory and ...

Elanco

Global Quality Auditor Lead

Indianapolis, IN · Hybrid

Global Quality Auditor Lead As a Global Quality Auditor Lead, you will be part of the Elanco Global ... In this role, you'll be responsible for ensuring that operations across commercial supply chains ...

TRIGO

Quality Manager

Detroit, MI

... TRIGO Global Quality Solutions Founded in 1997, TRIGO is a multinational company providing operational Quality Management solutions for the manufacturing sector, especially in the automotive and ...

TRIGO

Quality Manager

Greer, SC

... TRIGO Global Quality Solutions Founded in 1997, TRIGO is a multinational company providing operational Quality Management solutions for the manufacturing sector, especially in the automotive and ...

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All JobsGlobal Quality Operations Jobs

Global Quality Operations information

See salary details

$38.5K

$91K

$138.5K

How much do global quality operations jobs pay per year?

As of Jun 9, 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.

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 are 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, and why are they important?

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.
More about Global Quality Operations jobs
What job categories do people searching Global Quality Operations jobs look for? The top searched job categories for Global Quality Operations jobs are:
Global Quality Operations jobs near you
Infographic showing various Global Quality Operations job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 83% Full Time, 15% Part Time, and 1% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $91,047 per year, or $43.8 per hour.

Sr. Director, Quality Operations

kindeva

Bridgeton, MO • On-site

Other

Posted 25 days ago

Kindeva rating

6.8

Company rating: 6.8 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

Job description

Our Work Matters

At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.

The Impact You Will Make

Sr. Director of Quality Operations is responsible for leading all Quality Assurance (QA) functions at the St. Louis GMP manufacturing focused in sterile fill-finish drug products and combination products. This commercial facility operates as a Contract Manufacturing Organization (CMO), providing services to global clients. The role ensures full compliance with regulatory requirements while fostering a culture of quality, operational excellence, and inspection readiness.

ROLE RESPONSIBILITIES

  • Provide overall leadership for the site Quality operations organization
  • Act as a key member of the site leadership team, ensuring alignment of quality with manufacturing, engineering, supply chain, and regulatory functions.
  • Drive a culture of compliance, data integrity, and continuous improvement across the site.
  • Represent the site in global quality governance to ensure harmonization of systems and processes.
  • Ensure timely batch release decisions in alignment with cGMPs, regulatory standards, and client expectations.
  • Direct preparation for and management of regulatory inspections and client audits.
  • Provide oversight of deviations, CAPAs, change controls, and risk management.
  • Ensure compliance with combination product quality requirements (drug-device interface).
  • Ensure site operations comply with FDA, EMA, ICH, ISO 13485, and other global requirements.
  • Serve as the primary contact for regulatory inspections and audits.
  • Stay ahead of evolving regulations and implement proactive compliance strategies.
  • Lead, develop, and mentor QA teams to build a high-performing organization.
  • Establish clear roles, career pathways, and succession planning for Quality leadership.
  • Promote collaboration, open communication, and accountability across all functions.

 

 BASIC QUALIFICATIONS

Education and Experience

  • Bachelor’s degree in Life Sciences, Pharmacy, Engineering, or related field (advanced degree preferred).
  • 15+ years of progressive GMP Quality experience, including at least 8 years in sterile drug product manufacturing.
  • Combination product experience required.
  • Demonstrated success in leading Quality organizations and hosting regulatory inspections.

Skills

  • Expert knowledge of cGMPs, Annex 1, ISO 13485, ICH guidelines, and combination product regulations.
  • Strong leadership, influencing, and organizational skills.
  • Proven ability to implement process improvements and lead through change.
  • Excellent problem-solving and decision-making capabilities.
  • High ethical standards and professional integrity

PHYSICAL QUALIFICATIONS

  • Position requires vision acuity testing and onsite attendance – this position cannot be performed on a remote or telecommute basis on a temporary, short- or long-term basis.
  • The candidate must be able to complete aseptic gowning qualification and work in a Grade A/B classified area.
  • It is required to sit, stand and occasionally lift items (up to ~25 pounds), performing the duties of this position.
  • Must have the ability to simultaneously multi-task across multiple capabilities and functions and handle multiple competing priorities and requirements, including performing site and functional responsibilities, responding to frequent e-mail and phone communications, and attending multiple meetings and conference calls. Note that these activities may not be time bound to core hours or presence at the site.

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