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Iso Quality Manager Jobs (NOW HIRING)

CSafe Global

Quality Manager

Monroe, OH · On-site

In this high-impact role, you will ensure compliance with FDA, ISO 9001, ISO 13485, CE, and other ... Management Representative of the Quality Management System; develop, improve, and implement key ...

W3Global Inc.

Quality Manager

Germantown, WI · On-site

$90K - $110K/yr

Position Summary:- The Quality Manager will oversee all quality assurance and quality control ... Familiarity with ISO quality standards and manufacturing best practices. * Proven leadership ...

Hikinex

Quality Manager

Springfield, MO · On-site

Direct experience with IATF or ISO quality management systems. * Strong statistical background. * Demonstrated Lean Manufacturing experience. * Proven continuous improvement experience. * Strong ...

HIKINEX

Quality Manager

Springfield, MO · On-site

Direct experience with IATF or ISO quality management systems. * Strong statistical background. * Demonstrated Lean Manufacturing experience. * Proven continuous improvement experience. * Strong ...

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Iso Quality Manager information

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$24K

$86.2K

$158K

How much do iso quality manager jobs pay per year?

As of Aug 1, 2026, the average yearly pay for iso quality manager in the United States is $86,159.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,000.00 and $136,000.00 per year, depending on experience, location, and employer.

What is the difference between Iso Quality Manager vs Quality Assurance Specialist?

AspectIso Quality ManagerQuality Assurance Specialist
CertificationsISO 9001 Lead Auditor, ISO 14001 Lead AuditorASQ CQE, ISO 9001 Internal Auditor
Work EnvironmentOversees ISO compliance across departments, audits, documentationPerforms product and process testing, audits, and quality checks
Industry UsageManufacturing, aerospace, automotive, healthcareManufacturing, software, healthcare, consumer goods

The Iso Quality Manager focuses on implementing and maintaining ISO standards organization-wide, including audits and compliance. The Quality Assurance Specialist concentrates on testing, inspections, and ensuring product quality. Both roles require quality certifications but differ in scope and responsibilities within the quality management system.

What are the key skills and qualifications needed to thrive as an ISO Quality Manager, and why are they important?

To thrive as an ISO Quality Manager, you need in-depth knowledge of ISO standards (such as ISO 9001), quality management systems, and auditing procedures, often supported by a relevant degree and ISO certification. Familiarity with quality management software, document control systems, and auditing tools is typically required. Strong leadership, problem-solving abilities, and effective communication skills help drive continuous improvement and ensure compliance. These competencies are crucial to maintain high-quality standards, achieve certification, and support organizational excellence.

What are the typical challenges faced by an ISO Quality Manager when implementing and maintaining ISO standards within an organization?

ISO Quality Managers often encounter challenges such as gaining buy-in from staff across departments, ensuring consistent compliance with evolving ISO standards, and effectively communicating the importance of quality management processes. They must also regularly audit internal processes, address non-conformities, and coordinate corrective actions while balancing daily operational demands. Successful ISO Quality Managers collaborate closely with cross-functional teams, providing training and support to foster a culture of continuous improvement.

What does an ISO Quality Manager do?

An ISO Quality Manager is responsible for developing, implementing, and maintaining an organization's quality management system in compliance with ISO standards, such as ISO 9001. They oversee internal audits, lead improvement initiatives, and ensure that procedures meet both regulatory and customer requirements. Their role often includes training staff, analyzing quality data, and working with different departments to achieve and maintain ISO certification. This position is key to ensuring consistent product or service quality and ongoing organizational improvement.
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Iso Quality Manager jobs near you
Infographic showing various Iso Quality Manager job openings in the United States as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $86,159 per year, or $41.4 per hour.

Quality Manager

CSafe Global

Monroe, OH • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 13 days ago

Job description

Exciting Opportunity for a Quality Manager in the Cutting-Edge Cold Chain Solutions Industry!

Are you a quality-focused leader with expertise in regulatory compliance and continuous improvement? Join our team as a Quality Manager and lead the development, implementation, and oversight of our Quality Management System. In this high-impact role, you will ensure compliance with FDA, ISO 9001, ISO 13485, CE, and other applicable standards, while partnering with Manufacturing, Engineering, Supply Chain, and Regulatory teams to drive quality excellence across the organization. This is an opportunity to lead a talented team, influence strategic quality initiatives, and make a meaningful contribution to the success of our products and customers.


Essential Functions & Duties

  • Management Representative of the Quality Management System; develop, improve, and implement key quality system processes to ensure compliance with ISO 9001, ISO 13485, CE, TGA, and FDA 21 CFR 820.
  • Person Responsible for Regulatory Compliance (PRRC) for medical devices, ensuring device conformity to the quality management system and harmonized standards.
  • Ensures development, communication, implementation & maintenance of best-in-class quality management tools & principles.
  • Promotes continuous improvement.
  • Defines, communicates, and gains cross-functional support for the site's Quality System and compliance strategy to mitigate product and compliance risk.
  • Designs and implements effective quality processes including procedures, doc systems, CAPA, complaints, tools, reporting metrics and measurable improvements that are required to meet quality system standards and customer requirements.
  • Interface with customers, suppliers, and agencies as necessary.
  • Supervision of Quality Engineers and/or Technicians.
  • Manage the quality of a network of 3rd party manufacturing and distribution locations.
  • Manages Quality performance of our suppliers.

Knowledge, Skills & Abilities

  • Thorough knowledge of Quality tools (such as, but not limited to DOE, design of sampling plans, SPC, failure analysis, FMEA, DFMEA, etc.)
  • Strong interpersonal skills, both written and verbal.
  • Must possess analytical thinking and reasoning skills.
  • Must be thorough and exercise attention to detail.
  • Must be able to set and maintain schedules.
  • Must have good supervisory and mentoring skills.
  • Preferred certified auditor for ISO 9001, 13485 and FDA Quality System Regulations.

Education & Experience

  • Bachelor's degree in technical or scientific field, Engineering degree.
  • Advanced degree (Mechanical, Electrical, or Reliability) preferred.
  • Experience with FDA or ISO quality standards, including several completed ISO audits and FDA inspections.
  • 5 plus years' experience in Quality System and Compliance environment with at least 5 years in a managerial role.
  • Education/experience in one of the following:
    • a diploma, certificate or other evidence of formal qualification, awarded on completion of a university degree or of a course of study recognized as equivalent in law, medicine, pharmacy, engineering or another relevent scientific discipline, and at least one year of professional experience in regulatory affairs or in quality management systems relating to medical devices.
    • four years of professional experience in regulatory affairs or in quaity management systems relating to medical devices
  • Experience in medical device manufacturing, preferably a class II device.
  • Experience with FDA and ISO quality standards, including several completed ISO audits and FDA inspections.

Why Join Us?

At CSafe, we foster an exciting, collaborative, and inclusive work environment that promotes both personal and professional growth. Here’s what we offer to our employees:

  • Paid Time OFF (PTO) starting at 25 days & Paid Holidays
  • Medical, Dental and Vision Insurance
  • 401k with Employer Match
  • Group Life & Disability
  • Health Spending Account Options
  • Identity Protection
  • Employee Assistance Program
  • Travel Assistance Program
  • Financial Wellness Program
  • Tuition Reimbursement
  • Parental Leave
  • Referral Program
  • Gym Membership Reimbursement

An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.