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Quality Management System Auditor Jobs (NOW HIRING)

... Management System auditing standards and procedures. * In depth knowledge of and ability to apply quality system regulation including QSR, ISO 13485, MDSAP,cGMP Regulations, MDR and IVDR and other ...

... Management System auditing standards and procedures. * In depth knowledge of and ability to apply quality system regulation including QSR, ISO 13485, MDSAP,cGMP Regulations, MDR and IVDR and other ...

H&H is seeking a Quality Auditor to join the New Haven office and support the firm's quality management systems and project delivery processes. The Quality Auditor will assist with compliance audits ...

H&H is seeking a Quality Auditor to join the New Haven office and support the firm's quality management systems and project delivery processes. The Quality Auditor will assist with compliance audits ...

Serve as Lead Auditor & Trainer for the Quality Management System. * Oversee the maintenance of and adherence to industry, customer, and internal standards. * Oversee the Quality System auditing ...

Senior Quality Systems Engineer

Auburn Hills, MI · On-site

$83K - $113K/yr

This may include auditing to ensure compliance although this may be carried out by a third-party accredited body. DUTIES AND RESPONSIBILITIES: * Develop and sustain the Quality Management System in ...

Worker Type Regular Summary The Quality Management and Improvement Internal Auditor is responsible for performing quality management systems audits (product, process, or systems) at several AV ...

The Quality Management System (QMS) department creates, supports, and oversees the company's global ... The Quality Auditor is responsible for creating and carrying out detailed quality audit plans ...

Quality Internal Auditor

Memphis, TN · On-site

$54K - $58K/yr

This position supports the Quality Management System through the execution of internal audits ... At least 1 year of internal auditing and regulatory compliance experience. * Experience supporting ...

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Quality Management System Auditor information

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How much do quality management system auditor jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for quality management system auditor in the United States is $38.60, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $32.69 per hour, depending on experience, location, and employer.

What are some typical challenges faced by Quality Management System Auditors and how can they be managed?

Quality Management System Auditors often face challenges such as resistance to change from employees, complex or poorly documented processes, and staying updated on evolving regulatory standards. These can be managed by building strong relationships with team members, using clear and constructive communication, and committing to continuous professional development. Adaptability, professionalism, and a solutions-oriented mindset are essential for overcoming obstacles and driving positive process improvements. Being proactive and open to feedback also helps auditors foster a culture of compliance and quality across the organization.

What are the key skills and qualifications needed to thrive in the Quality Management System Auditor position, and why are they important?

To thrive as a Quality Management System Auditor, you need a strong understanding of quality standards (such as ISO 9001), process auditing, and document control, often supported by a relevant degree and industry-recognized certifications like ISO Lead Auditor. Familiarity with audit management software, document management systems, and compliance tracking tools is typically required. Attention to detail, analytical thinking, and effective communication skills are critical soft skills for investigating processes and reporting findings. These competencies ensure that audits are thorough, compliance risks are identified, and organizational improvements are consistently achieved.

What is a Quality Management System Auditor job?

A Quality Management System (QMS) Auditor is responsible for evaluating an organization's quality management processes to ensure compliance with industry standards, regulations, and internal policies. They conduct audits, review documentation, identify nonconformities, and recommend corrective actions to improve efficiency and compliance. QMS Auditors work in various industries, such as manufacturing, healthcare, and technology, and often need certifications like ISO 9001 Lead Auditor. Their role helps organizations maintain consistency, enhance product or service quality, and meet customer and regulatory requirements.

More about Quality Management System Auditor jobs
What cities are hiring for Quality Management System Auditor jobs? Cities with the most Quality Management System Auditor job openings:
What states have the most Quality Management System Auditor jobs? States with the most job openings for Quality Management System Auditor jobs include:
Infographic showing various Quality Management System Auditor job openings in the United States as of May 2026, with employment types broken down into 95% Full Time, and 5% Contract. Highlights an 100% In-person job distribution, with an average salary of $80,278 per year, or $38.6 per hour.
Quality Management System Lead

Quality Management System Lead

HP Development Company, L.P.

Corvallis, OR • On-site

$116K - $182K/yr

Full-time

Medical, Dental, Vision, Life, PTO

Posted 18 days ago


Job description

Quality Management System Lead
Description -
We are seeking an experienced Quality Management System (QMS) Lead to drive the development, implementation, and sustainability of a robust QMS. This role will support the product development lifecycle and future EUPIA/GMP manufacturing requirements across various technology platforms & work centers.
This is an expert-level, highly visible role that requires deep systems expertise, strong cross-functional leadership, and the ability to influence priorities and behaviors to move the organization toward a documented, trained, and continuously improving system. This role will ensure that quality is embedded into everyday behaviors and processes and that the QMS is a practical and useful tool.
Responsibilities
QMS Development & Ownership
  • Own the overall QMS strategy and roadmap. Lead the development, rollout, and sustainment of QMS modules aligned to ISO 9001 and EUPIA/GMP requirements (e.g., CAPA, audits, change management, training, document control, records management, process control).
  • Define the QMS framework and tiered documentation structure (policies, procedures, records), ensuring consistency and scalability across programs and organizations.
  • Ensure QMS modules support both product development and manufacturing readiness.
  • As required, develop and own QMS modules and systems before handing off to long-term owners.
  • Work with management to identify and resolve resource needs associated with QMS.
  • Serve as the subject matter expert on quality system standards and interpretations
  • Align the QMS with adjacent organizations. Serve as a resource for other QMS efforts.

Implementation & Adoption
  • Partner with engineering, operations, and program leadership to embed QMS requirements into existing workflows.
  • Support rollout of QMS practices into new areas beyond initial pilot groups.
  • Reinforce behaviors through audits, metrics, and management reviews-not documentation alone.
  • Ensure that the QMS efforts focus on usefulness and not check-the-box compliance.

Metrics, Reviews & Continuous Improvement
  • Define, track and integrate QMS-related metrics to existing meetings and review systems
  • Lead & support QMS management reviews and executive sponsor updates.
  • Identify systemic gaps and drive continuous improvement across processes and systems.

Required Qualifications and/or Experiences
  • Bachelor's degree in Engineering, Quality, Manufacturing, or related field (or equivalent experience).
  • Previous experience building, implementing, and/or sustaining Quality Management Systems in an R&D and/or manufacturing environment.
  • Working knowledge of ISO 9001; familiarity with EUPIA/GMP, GMP, or other regulated quality systems (medical, pharma, food, or similar).
  • Experience with CAPA systems, internal audits, and document control.
  • Understanding of product development processes, control plans and change management systems.

Preferred Experience and Skills
  • Ability to translate standards and regulatory language into clear, usable processes.
  • Strong systems thinking - able to see interactions between systems, metrics, and behaviors.
  • Strong understanding of Project Management Fundamentals, SPC & manufacturing processes.
  • Excellent verbal and written communication skills, with the ability to influence at all levels of the organization without authority.
  • Experienced with working with partners across all levels - including, but not limited to: operations, engineers, management, and Southeast Asia.
  • Project and program leadership skills; able to drive progress across multiple parallel efforts.
  • Comfortable working through ambiguity and evolving requirements
  • Prior experience supporting audits & certification
  • Experience with tiered documentation frameworks.
  • Familiarity with document management system (e.g. DMS) and electronic change management tools (e.g., Windchill).
  • Previous Product/Quality Engineering experiences

The pay range for this role is $116,150 to $182,400 USD annually with additional opportunities for pay in the form of bonus and/or equity (applies to United States of America candidates only). Pay varies by work location, job-related knowledge, skills, and experience.
Benefits:
HP offers a comprehensive benefits package for this position, including:
  • Health insurance
  • Dental insurance
  • Vision insurance
  • Long term/short term disability insurance
  • Employee assistance program
  • Flexible spending account
  • Life insurance
  • Generous time off policies, including;
  • 4-12 weeks fully paid parental leave based on tenure
  • 11 paid holidays
  • Additional flexible paid vacation and sick leave (US benefits overview)

The compensation and benefits information is accurate as of the date of this posting. The Company reserves the right to modify this information at any time, with or without notice, subject to applicable law.
Job -
Engineering
Schedule -
Full time
Shift -
Shift 1, 0% premium (United States of America)
Travel -
Relocation -
Equal Opportunity Employer (EEO) -
HP, Inc. provides equal employment opportunity to all employees and prospective employees, without regard to race, color, religion, sex, national origin, ancestry, citizenship, sexual orientation, age, disability, or status as a protected veteran, marital status, familial status, physical or mental disability, medical condition, pregnancy, genetic predisposition or carrier status, uniformed service status, political affiliation or any other characteristic protected by applicable national, federal, state, and local law(s).
Please be assured that you will not be subject to any adverse treatment if you choose to disclose the information requested. This information is provided voluntarily. The information obtained will be kept in strict confidence.
For more information, review HP's EEO Policy or read about your rights as an applicant under the law here: "Know Your Rights: Workplace Discrimination is Illegal"