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Director Quality Jobs (NOW HIRING)

Position Summary The Director, Quality is responsible for leading multiple manufacturing/service sites and/or corporate quality resources in the execution of the overall STERIS Quality System. This ...

Director Quality Location: Las Cruces, NM Employment Type: Full-Time Salary Range: As per Exp. Benefits: Medical, Dental, Vision, Life Insurance, Retirement Plan, Paid Time Off, and more Position ...

Director Quality Are you passionate about quality and committed to excellence? Consider joining our Tidelands Health team. As our region's largest health care provider, we are also one of our area ...

The Director of Quality provides overall organizational leadership for performance improvement and will develop and foster effective collaboration between all departments and other affiliated ...

The Director, Quality Systems & Restricted Material Compliance will define and execute the multi-year strategy, governance, and evolution of the company's global Quality Management System (QMS) and ...

The Director, Quality Assurance ensures that all Topps and Fanatics Collectibles products are manufactured to the highest standards of quality, integrity, and timeliness. The Director will focus on ...

The Business Unit Quality Director is responsible for leading all quality performance, execution, and results within an assigned Business Unit. This role ensures that quality is fully integrated into ...

The Quality Director is accountable for leading and continuously improvingbusinessgroupwidequality assuranceprogrammesfor Large Megawatt (LMW) generator integration in ahighmixmanufacturing ...

The Business Unit Quality Director is responsible for leading all quality performance, execution, and results within an assigned Business Unit. This role ensures that quality is fully integrated into ...

Itron is seeking a Director, Global Manufacturing Quality. Reporting to the Vice President of Global Quality, this executive will lead operational execution and strategic alignment globally ...

The Director, Quality Systems & Restricted Material Compliance will define and execute the multi-year strategy, governance, and evolution of the company's global Quality Management System (QMS) and ...

Director Quality

Sacramento, CA · On-site

$66.26 - $98.56/hr

One California Job Summary and Responsibilities As our Director of Quality at Mercy General Hospital, you'll lead ongoing quality improvement initiatives that include collaboration between many ...

Director, Quality Location: United States-North Carolina-Greensboro-Aircraft Reconfig Technologies Job Number: 18310 Position Overview The Director of Quality is responsible for ensuring ...

Position Overview The Director of Quality is responsible for ensuring organizational compliance with applicable regulatory guidelines through the development, implementation, and oversight of the ...

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Director Quality information

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$31K

$125.6K

$213.5K

How much do director quality jobs pay per year?

As of Jun 6, 2026, the average yearly pay for director 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 does a Director of Quality do?

A Director of Quality oversees the quality assurance and quality control processes within an organization to ensure that products or services meet established standards and regulatory requirements. They develop and implement quality management systems, lead teams responsible for inspections and audits, and work closely with other departments to promote continuous improvement. The Director of Quality also analyzes quality data, manages compliance with industry regulations, and often interacts with customers or external auditors to address quality concerns.

What are the key skills and qualifications needed to thrive as a Director of Quality, and why are they important?

To succeed as a Director of Quality, you need extensive knowledge in quality management systems, regulatory compliance, and process improvement, often supported by a bachelor's or master's degree in a relevant field. Familiarity with tools such as Six Sigma, ISO standards, and quality auditing software, along with certifications like CQE or Six Sigma Black Belt, is typical. Exceptional leadership, analytical thinking, and effective communication are critical soft skills for driving quality initiatives and leading cross-functional teams. These competencies ensure organizational standards are upheld, continuous improvement is achieved, and regulatory risks are minimized.

What is the difference between Director Quality vs Quality Manager?

AspectDirector QualityQuality Manager
CredentialsBachelor's or Master’s in Quality Management, Engineering, or related field; certifications like ASQ CQE or CQABachelor's in Quality, Engineering, or related; certifications like ASQ CQE or CQA often preferred
Work EnvironmentStrategic leadership in quality initiatives, overseeing multiple departments or sitesOperational focus, managing daily quality processes and teams
Employer & Industry UsageUsed in manufacturing, healthcare, aerospace, and industries with complex quality systemsCommon in manufacturing, production, and service industries

The main difference between a Director Quality and a Quality Manager lies in their scope and strategic focus. The Director Quality typically oversees the entire quality program at a higher level, setting policies and long-term goals, while the Quality Manager handles daily operations and implements quality procedures. Both roles require similar credentials and certifications, but their responsibilities and strategic influence differ significantly.

How does a Director of Quality typically collaborate with cross-functional teams to drive continuous improvement initiatives?

A Director of Quality plays a key role in partnering with departments such as manufacturing, engineering, supply chain, and regulatory affairs to identify and resolve process inefficiencies and ensure compliance with quality standards. They often lead cross-functional meetings, facilitate root cause analyses, and champion a culture of continuous improvement by implementing best practices and quality tools like Six Sigma or Lean methodologies. Effective communication and the ability to influence stakeholders at all levels are essential, as the Director of Quality ensures that all departments are aligned with organizational quality goals and regulatory requirements.
More about Director Quality jobs
What cities are hiring for Director Quality jobs? Cities with the most Director Quality job openings:
What are the most commonly searched types of Quality jobs? The most popular types of Quality jobs are:
What states have the most Director Quality jobs? States with the most job openings for Director Quality jobs include:
Director, Quality

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted yesterday


STERIS rating

8.3

Company rating: 8.3 out of 10

Based on 128 frontline employees who took The Breakroom Quiz

44th of 867 rated healthcare providers


Job description

Position Summary
The Director, Quality is responsible for leading multiple manufacturing/service sites and/or corporate quality resources in the execution of the overall STERIS Quality System. This position is principally responsible for manufacturing/service site or functional quality system execution to drive product/service quality improvement and to be compliant with, as appropriate, the following standards: IS0 9001, ISO 13485, MDSAP and CFR Part 820/211, EU MDR, and other applicable standards. The Quality Director will lead teams of quality managers and engineers responsible for product and service quality, supplier quality, new product/service support, continuous improvement support, and quality system execution.
What You'll do as a Director Quality
  • The Director, Quality will have responsibility for the following: Leads manufacturing/service sites and/or corporate quality staff in the execution and continuous improvement of the STERIS Quality System. Operates with a focus on the following objectives:
    • Ensures site level compliance to appropriate ISO, FDA, and other applicable regulatory standards.
    • Drives strategies and methods to continuously improve capital, consumable and service product quality performance.
    • Establishes clear and consistent quality measurement systems in order to monitor and drive results.
    • Leads quality planning and the execution of assigned New Product/Service Development (NPD) projects to achieve targeted quality deliverable adherence.
    • Drives targeted supplier quality improvement efforts and oversees supplier evaluation, approval, and control for assigned manufacturing sites.
    • Assists in the continuous improvement and standardization of quality system procedures and monitor effectiveness.
    • Supports the reliability function by integrating design for reliability tools and techniques within the local projects.
    • Leads quality planning efforts through cross-functional teaming at a site level.
  • Supports the New Product/Service Development process and projects to ensure projects attain cost, quality, and delivery objectives.
  • Directs local staff on planning sequential and concurrent quality activities. Establish planning and monitoring tools and techniques.
  • Provides Quality viewpoints and opinions in planning and specifying existing and future products.
  • Assists in the development of the Quality budget. Helps to ensures resources are adequate to fully support the Quality System.
  • Takes ownership of all local quality issues, projects, and development activities. Works closely with the site's Senior Management Teams to provide strategic direction and development of the manufacturing sites product quality strategies and tactics.
  • Manages and provide direction to a teams of quality professionals both at corporate and manufacturing sites, with responsibility for hiring, performance management, appropriate staffing, and deployment of resources.
  • Assures that local sites maintain and improve operational and quality systems to remain in a state of compliance to appropriate ISO, FDA, and other applicable regulatory standards.
  • Works closely with the regulatory function to ensure compliance to appropriate ISO and FDA standards; plans for and assists in the management of external audits.
  • Leads manufacturing and service site quality teams to ensure alignment to operations, support of Lean efforts and drive quality improvement performance for products, services, and processes across the sites.
  • This individual has autonomy to perform the duties of Person Responsible for Regulatory Compliance (PRRC) on behalf of STERIS legal manufacturing entities under the EU MDR. This individual shall suffer no disadvantage within the organization in relation to proper fulfilment of his or her duties in lieu of article 15 of the EU MDR.

The Experience, Skills, and Abilities Needed
Required:
  • Bachelor's Degree (Engineering or related technical field).
  • Minimum 10 years of experience with increased responsibility leading quality system and product quality improvement efforts. Exceptional leadership manifested through organizing and motivating teams toward their respective goals by employing hands-on management.
  • Must fulfil the experience requirements listed in Article 15 of the EUMDR (PRRC).
  • A solid quality foundation indicated by a demonstrated understanding of Lean/Six Sigma, quality system, and product/process improvement methodologies.
  • Solid business acumen and proven ability to build and lead process and product improvement strategies and results.
  • Strong expertise in analytical methods, quality systems, and continuous improvement methods.
  • Excellent interpersonal, as well as verbal and written communication skills in order to develop and maintain rapport and effective internal and external relationships to support business success.
  • The ability to work hard and deliver results under pressure, as well as the willingness to address and shift priorities in rapidly changing markets.

Preferred:
  • Advanced degree.
  • Experience in medical device industry.
  • Experience with statistical analysis software and Visio.

Other:
  • Excellent problem-solving skills.
  • Focus on identification of potential issues and continuous improvement.
  • Experience working on cross-functional teams and on own initiative.
  • Demonstrated excellent organizational, oral, and written communications skills.
  • Must have PC experience, as well as working familiarity of desktop applications including Excel, Word, and PowerPoint.

What STERIS Offers
We value our employees and are committed to providing a comprehensive benefits package that supports your health, well-being, and financial future.
Here is a brief overview of what we offer:
  • Market competitive pay
  • Extensive paid time off and (9) added holidays
  • Excellent healthcare, dental, and vision benefits
  • Long/short term disability coverage
  • 401(K) with company match
  • Maternity and parental leave
  • Additional add on benefits/discounts for programs such as pet insurance
  • Tuition reimbursement and continued educational programs
  • Excellent opportunities for advancement in a stable long-term career

#LI-HT
Pay range for this opportunity is $150,000 - $187,000. This position is eligible for bonus participation.
Minimum pay rates offered will comply with county/city minimums, if higher than range listed. Pay rates are based on a number of factors, including but not limited to local labor market costs, years of relevant experience, education, professional certifications, foreign language fluency, etc.
STERIS offers a comprehensive and competitive benefits portfolio. Click here for a complete list of benefits: STERIS Benefits
Open until position is filled.
STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention. WE HELP OUR CUSTOMERS CREATE A HEALTHIER AND SAFER WORLD by providing innovative healthcare and life sciences products and services around the globe. For more information, visit www.steris.com.
If you need assistance completing the application process, please call 1 (440) 392.7047. This contact information is for accommodation inquiries only and cannot be used to check application status.
STERIS is an Equal Opportunity Employer. We are committed to equal employment opportunity to ensure that persons are recruited, hired, trained, transferred and promoted in all job groups regardless of race, color, religion, age, disability, national origin, citizenship status, military or veteran status, sex (including pregnancy, childbirth and related medical conditions), sexual orientation, gender identity, genetic information, and any other category protected by federal, state or local law. We are not only committed to this policy by our status as a federal government contractor, but also we are strongly bound by the principle of equal employment opportunity.
The full affirmative action program, absent the data metrics required by § 60-741.44(k), shall be available to all employees and applicants for employment for inspection upon request. The program may be obtained at your location's HR Office during normal business hours.

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