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Director Quality Management Jobs (NOW HIRING)

Director, Quality Systems

San Diego, CA · On-site

$170K - $210K/yr

The Director Quality Systems will lead and support quality assurance and quality systems activities ... The role advances the company's Quality Management System, drives inspection readiness, and ensures ...

This role includes both direct and indirect people management and leadership responsibilities. The position requires up to 50% travel across the US. Responsibilities Quality Systems & SOP Governance

Provide leadership and direction to site Quality Managers and teams,Partnering with Site ... Partner with the Director of Quality Systems to implement system improvements and provide feedback ...

Reporting to the Director, Quality, you are an essential member of the In-Lab quality management team and responsible for the overall quality performance at two locations, Heath & Hebron In-Labs.

IL · On-site

$160K - $175K/yr

The Director, Quality Operations is responsible for supporting the development and implementation ... Implements key quality strategies, including initiation and management of provider, member and/or ...

Showing results 41-60

Director Quality Management information

See salary details

$31K

$125.6K

$213.5K

How much do director quality management jobs pay per year?

As of Sep 3, 2026, the average yearly pay for director quality management 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 are the key skills and qualifications needed to thrive as a director of quality management?

To thrive as a Director of Quality Management, you need in-depth knowledge of quality assurance principles, regulatory compliance, process improvement methodologies, and typically a degree in a related field such as healthcare, engineering, or business. Familiarity with quality management systems (e.g., ISO 9001), data analytics tools, and relevant certifications like Certified Professional in Healthcare Quality (CPHQ) are often required. Exceptional leadership, communication, and problem-solving abilities enable effective collaboration across departments and drive organizational change. These skills ensure the organization consistently meets quality standards, improves outcomes, and mitigates risk.

How does a director of quality management typically collaborate with cross-functional teams to drive quality initiatives?

A Director of Quality Management works closely with teams across the organization, including operations, product development, regulatory affairs, and customer service, to implement and uphold quality standards. This role often leads cross-functional meetings, facilitates root cause analyses, and coordinates the rollout of process improvements. Effective communication and the ability to build consensus are crucial, as the Director must align diverse departments around shared quality goals. By fostering collaboration, the Director ensures that quality initiatives are integrated seamlessly into daily operations and long-term strategies.

What is the difference between Director Quality Management vs Quality Assurance Manager?

AspectDirector Quality ManagementQuality Assurance Manager
ResponsibilitiesOversees entire quality management systems, develops policies, and ensures compliance across departments.Implements quality assurance processes, monitors product quality, and manages QA teams.
CertificationsISO 9001 Lead Auditor, Six Sigma, CQEISO 9001 Lead Auditor, Six Sigma, CQE
Work EnvironmentStrategic, cross-departmental, executive-levelOperational, team-focused, project-based
Industry UsageCommon in manufacturing, healthcare, and large organizationsPrevalent in manufacturing, software, and service industries

While both roles focus on quality, the Director of Quality Management has a broader, strategic oversight role, whereas the Quality Assurance Manager concentrates on implementing and managing specific QA processes within teams.

What does a director of quality management do?

A director of quality management oversees an organization’s quality assurance and control processes to ensure products or services meet industry standards and customer expectations. They develop quality policies, lead audits, analyze data for continuous improvement, and coordinate with departments to implement quality initiatives, often requiring knowledge of quality management systems like ISO and leadership skills. The role typically involves strategic planning, team management, and ensuring compliance with regulatory requirements.

What cities are hiring for Director Quality Management jobs?

Cities with the most Director Quality Management job openings:

What are the most commonly searched types of Quality Management jobs?

The most popular types of Quality Management jobs are:

What states have the most Director Quality Management jobs?

States with the most job openings for Director Quality Management jobs include:

Infographic showing various Director Quality Management job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 13% Part Time, and 2% Contract. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution, with an average salary of $125,600 per year, or $60.4 per hour.

Regional Manager, Quality Management

Cardinal Health

Sharon Hill, PA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 10 days ago


Cardinal Health rating

7.8

Company rating: 7.8 out of 10

Based on 340 frontline employees who took The Breakroom Quiz

135th of 898 rated healthcare providers


Job description

What Quality Management contributes to Cardinal Health

Quality develops and implements quality policies, procedures, and processes to ensure products and services comply with regulatory standards and specifications.


Quality Management provides strategic oversight, leadership and direction within the Quality function.

Cardinal Health PET Manufacturing Services is responsible for manufacturing PET radiopharmaceuticals to enhance patient treatment through improved disease diagnosis, staging, and monitoring.

Responsibilities

  • Provides overall direction and management of the QA function that supports their assigned PET manufacturing sites in the United States
  • Is responsible for all Quality Assurance functions including but not limited to: raw material storage activities, batch record review and approval, product disposition, investigation and remediation of manufacturing issues according to procedure, compliant investigation, execution of validation protocols and site related records management
  • Provides advice, guidance and training to QA staff in the verification and approval of documents and processes including but not limited to: validation protocols / reports, investigations, procedures and change controls
  • Providing general oversight to ensure the identity, strength, quality and purity of the drug product released at their sites
  • Ensuring that all raw materials and finished product meet specifications
  • Ensuring the review of production records and release of finished product at their assigned sites
  • Ensuring that all procedures are followed and that all errors and failures to meet specification are appropriately investigated and corrected at their sites
  • Ensuring regional quality coverage at all assigned sites
  • Interacts with regulatory agencies, as necessary and ensures the closure any regional FDA commitments on time and its related documentation/objective evidence appropriate
  • Ensure that the procedures are properly followed and adequate for their intended use
  • Implements and monitors quality performance measures for the site and reports them to the Director, Quality in a timely manner
  • Interacts with and provides advice to management and other personnel in the establishment of systems, plans, specifications, methods and procedures
  • Assess data collected (complaints, investigations, change control, stability failures, etc.) to identify trends and develop corrective actions where needed to ensure compliance with cGMP’s and regulatory requirements
  • Collaborates with their assigned Area Manager and others to build strategic alliances within the PET network; negotiates to build broad-based support and/or persuades others in order to meet deadlines
  • Identifies opportunities to improve efficiency while providing flawless transactions, services and products; manages monetary assets and other resources to optimize cost effectiveness
  • Ensures that customers have a positive experience; commits to meet or exceed customer expectations
  • The Regional Quality Manager (RQM) has the authority to:
    • Approves change control documents (up to a moderate change)
    • Initiates investigations and provide direction for corrective action
    • Determines, develops and delivers training
    • Develops, reviews and revises quality procedures
    • Makes hiring decisions for their direct reports
    • Approves personnel related issues (PTO, travel, etc.)
    • Deploys employee goals, objectives and performance evaluations
    • Carries out other duties as described in policies and procedures or as assigned by the Director/Quality

Qualifications

  • Bachelor’s degree in related field, or equivalent work experience, preferred
  • 8-12 years of experience, preferred
  • 2-5 years of experience in the Pharmaceutical Industry preferred
  • 1-3 years of experience in a quality management role preferred
  • Thorough knowledge of FDA regulatory requirements, controlled environments, good manufacturing practices and quality system requirements
  • Knowledgeable to validation practices and principles
  • Excellent interpersonal, organizational and communication skills
  • Demonstrated leadership and the ability to motivate and influence others
  • Proficiency with MS Word, PowerPoint and Excel (statistics, graphing, presentations, etc.)
  • Proactively develops and maintains technical knowledge in specialized area(s), remaining up-to-date on current trends and best practices
  • Ability to travel to all assigned sites (50%-75%)
  • Must be located near PET facility or relocation may be required

What is expected of you and others at this level

  • Manages department operations and supervises professional employees, front line supervisors and/or business support staff
  • Participates in the development of policies and procedures to achieve specific goals
  • Ensures employees operate within guidelines
  • Decisions have a short term impact on work processes, outcomes and customers
  • Interacts with subordinates, peers, customers, and suppliers at various management levels; may interact with senior management
  • Interactions normally involve resolution of issues related to operations and/or projects
  • Gains consensus from various parties involved

Schedule

  • Onsite role at a PET manufacturing facility
  • Candidate must be flexible to work different shifts or schedules based on business need
  • Work hours may be subject to change
  • 50% - 75% travel

Work Environment

  • The primary work environment consists of a manufacturing pharmacy which must be kept clean, orderly, properly lighted and maintained in optimum operating condition. Employees handle radioactive materials and are exposed to very low amounts of radiation that are deemed safe by current standards. The facility is operated under well-controlled and closely monitored conditions that are regulated by both State and Federal agencies, and that are enforced by the corporate internal quality and regulatory group. Each staff member will receive specific training in keeping radiation exposures within regulatory guidelines and he/she will be routinely monitored for their exposure to radiation. Noise levels are considered low to moderate.

Anticipated salary range: $105,100 - $150,100

Bonus eligible: Yes

Benefits: Cardinal Health offers a wide variety of benefits and programs to support health and well-being.

  • Medical, dental and vision coverage
  • Paid time off plan
  • Health savings account (HSA)
  • 401k savings plan
  • Access to wages before pay day with myFlexPay
  • Flexible spending accounts (FSAs)
  • Short- and long-term disability coverage
  • Work-Life resources
  • Paid parental leave
  • Healthy lifestyle programs

Application window anticipated to close: 08/24/2026 *if interested in opportunity, please submit application as soon as possible.

The salary range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate’s geographical location, relevant education, experience and skills and an evaluation of internal pay equity.

#LI-TF1

Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply.

Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law.


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About Cardinal Health

Sourced by ZipRecruiter

Cardinal Health Innovative Delivery Solutions With over 45 years of experience in helping hundreds of hospital and outpatient pharmacies, we provide access to best practice strategies and tactics to control costs, improve workflow and enhance safety. Cardinal Health Innovative Delivery Solutions is one of the largest employers of acute-care pharmacist in the United States. Cardinal Health is the employer of choice for pharmacists because we offer a variety of career opportunities in pharmacy leadership, clinical specialties, remote order entry, business management, medication therapy management and more.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Dublin, OH, US

Year founded

1971

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