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Director Global Quality Jobs (NOW HIRING)

Accra Conxt

Global Quality Director

Erlanger, KY · On-site

$150 - $200/hr

Global Quality Director Full Time Not Reported USPC Erlanger, Erlanger, KY, US 30+ days ago Requisition ID: 2196 As Global Quality Director for the Entertainment Business, you will set and lead the ...

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 ...

MSD

QMS Global Quality Compliance Director

Durham, NC · On-site

Job Summary The QMS Global Quality Compliance Director reports into the Associate Vice President, Global QMS and is a senior quality governance and compliance role responsible for driving strategy ...

MSD

QMS Global Quality Compliance Director

Wilson, NC · On-site

Job Summary The QMS Global Quality Compliance Director reports into the Associate Vice President, Global QMS and is a senior quality governance and compliance role responsible for driving strategy ...

Merck & Co.

Job Summary The QMS Global Quality Compliance Director reports into the Associate Vice President, Global QMS and is a senior quality governance and compliance role responsible for driving strategy ...

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How much do director global quality jobs pay per year?

As of Sep 8, 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, 14% Part Time, 3% Contract, and 1% Nights. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $125,600 per year, or $60.4 per hour.

Associate Director, Global Quality - API

Corden Pharma Colorado

Boulder, CO • On-site

$150K - $170K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 12 days ago

Key responsibilities

  • Support sites in GMP compliance, audits, and regulatory expectations related to API manufacturing.

  • Support inspection readiness, audits, and remediation activities, and monitor KPIs to identify risks.

  • Collaborate with sites on quality agreements, customer interactions, and drive continuous improvement of quality systems.

Job description

CordenPharma is a leading full-service Contract Development and Manufacturing Organization (CDMO) specializing in active pharmaceutical ingredients (APIs), excipients, drug products (DPs), and packaging. With around 3,000 employees worldwide, we help pharmaceutical and biotech companies manufacture medicines with the ultimate goal of improving people’s lives.
Our network, spanning Europe and the U.S., provides flexible and specialized solutions across six technology platforms: Peptides, Lipids & Carbohydrates, Injectables, Highly Potent & Oncology, Small Molecules, and Oligonucleotides. We strive for excellence in supporting this network and are committed to delivering the highest quality products for patient well-being.
Our People VisionWe strive for excellence. We share our passion. Together, we make a difference in patients' lives.

This role may be based in either Boulder, CO or N. Augusta, GA


SUMMARY

In this role, you act as a Global Quality Subject Matter Expert (SME) for API manufacturing, supporting sites across the network in GMP compliance, quality systems, and complex operational challenges. You work closely with local and global teams to ensure inspection readiness, robust processes, and consistent quality standards, while contributing hands-on to global quality initiatives and continuous improvement.

 

What makes this role relevant:

 

  • Strong expert role with global exposure across API sites
  • High impact on compliance, inspections, and quality systems
  • Focus on hands-on support, problem-solving, and continuous improvement


ESSENTIAL DUTIES AND RESPONSIBILITIES

Include the following. Other duties may be assigned.

 

Expert / Advisory (Focus)

  • Act as SME for API GMP compliance (EU & FDA) across the global network
  • Support sites on complex quality topics, audits, and regulatory expectations
  • Provide expertise on quality systems, process robustness, and QbD principles
  • Advise on and execute quality integration activities (e.g. new sites, acquisitions)
  • Deliver training and guidance on GMP standards and best practices
  • Create and implement Corporate Compliance Standards.


Operational

  • Support inspection readiness, audits, and remediation activities
  • Monitor KPIs and identify risks, driving appropriate corrective actions
  • Participate in quality escalations and ensure structured investigations & CAPAs
  • Collaborate with sites on quality agreements and customer interactions
  • Drive harmonization and continuous improvement of quality systems across sites

EDUCATION and/or EXPERIENCE 

BA or BS (scientific degree preferred) in Chemistry, Pharmacy, Engineering or related field from a four-year university; and 15 years’ experience in API quality, manufacturing or QA/QC; or equivalent combination of education and experience. Strong Quality background and experience is a must


CORE COMPETENCIES 

These are the specific areas of knowledge, skill and ability that are important for successful job performance. They must be job related and consistent with business necessity.


  • Strong expertise in EU GMP & FDA regulations
  • Hands-on experience with inspections, audits, and global quality systems
  • Proven track record as SME in API or CDMO environment
  • Strong stakeholder management and ability to work cross-functionally in global teams
  • Willingness to travel internationally (~40%)

SALARY

Actual pay will be based on your skills and experience.

 

BENEFITS

  • 401(k) matching - Corden Pharma will contribute 100% of the first 6% - 100% vested after 2 years of service 
  • Accident Plan
  • Critical Illness Insurance
  • Dental Insurance
  • Disability Insurance
  • Employee Assistance Program
  • Flexible Spending Account
  • Health Insurance PPO/HSA
  • Hospital Indemnity Plan
  • ID Theft Protection
  • Life Insurance
  • Paid Parental Leave
  • Tuition Reimbursement
  • Wellness Program
  • Vacation – Three Weeks 1st Year
  • Vision Insurance

 

EQUAL OPPORTUNITY EMPLOYER

Corden Pharma provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran stat