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Iso Quality Manager Jobs in Riverside, CA (NOW HIRING)

Fortive

Manager, Product Quality

Irvine, CA · On-site

Job Title Manager, Product Quality Job summary Leads a global team responsible for executing ... Part 820, ISO 13485, and EU MDR. - Experience in quality systems within medical device ...

Attalon, Inc.

Quality Coordinator

Tustin, CA · On-site

$23.01 - $39.35/hr

Familiarity with quality management systems such as ISO 9001, AS9100, or similar standards ... Knowledge of calibration management tools, procedures, or software is a plus. Key Competencies

Senra Systems

Quality Engineer

Santa Ana, CA

$95K - $140K/yr

Support the implementation and improvement of the company's Quality Management System. * Ensure ... Familiarity with AS9100 or ISO quality systems. * Experience supporting new product introductions ...

Senra Systems

Quality Engineer

Irvine, CA

$95K - $140K/yr

Support the implementation and improvement of the company's Quality Management System. * Ensure ... Familiarity with AS9100 or ISO quality systems. * Experience supporting new product introductions ...

Nihon Kohden America

Quality Systems Manager

Irvine, CA · On-site

$100K - $145K/yr

Strong knowledge of GxP, ISO 13485, ISO 14971, and FDA 21 CFR 820. * Able to apply Canadian Medical Devices Regulations SOR/98-282. * Knowledge of Quality Systems Software: Configuration Management ...

Nihon Kohden

Quality Systems Manager

Irvine, CA · On-site

$100K - $145K/yr

Strong knowledge of GxP, ISO 13485, ISO 14971, and FDA 21 CFR 820. * Able to apply Canadian Medical Devices Regulations SOR/98-282. * Knowledge of Quality Systems Software: Configuration Management ...

Nihon Kohden USA

Quality Systems Manager

Irvine, CA · On-site

$100K - $145K/yr

Strong knowledge of GxP, ISO 13485, ISO 14971, and FDA 21 CFR 820. * Able to apply Canadian Medical Devices Regulations SOR/98-282. * Knowledge of Quality Systems Software: Configuration Management ...

Nihon Kohden

Quality Systems Manager

Irvine, CA · On-site

$100 - $125/hr

Strong knowledge of GxP, ISO 13485, ISO 14971, and FDA 21 CFR 820. * Able to apply Canadian Medical Devices Regulations SOR/98-282. * Knowledge of Quality Systems Software: Configuration Management ...

TST MASTER

Quality Assurance Manager

Fontana, CA · On-site

$100K - $120K/yr

Experience in latest ISO Standard for quality management systems. * Proficient in problem solving techniques, including root cause analysis, process mapping, corrective and preventive action. * Near ...

TST MASTER

Quality Assurance Manager

Fontana, CA

Experience in latest ISO Standard for quality management systems. * Proficient in problem solving techniques, including root cause analysis, process mapping, corrective and preventive action. * Near ...

Terran Orbital Corporation

Quality Engineer

Irvine, CA · On-site

$77K - $99K/yr

Knowledge of machining, assembly operations, problem-solving, gauging, process capability, SPC, APQP, and quality management systems ISO and 9001 ASA9100. * Knowledge and experience with AIAG Core ...

Thermal-Vac

Quality Control Inspector

Anaheim, CA · On-site

$20 - $25/hr

This position reports to the Quality Manager and will perform receiving, in-process, and final ... We are ISO 9001 and AS9100 Registered, as well as Nadcap Certified, ensuring our commitment to ...

Flex

Quality Supervisor - Fabrication

Fontana, CA · On-site

$65K - $89K/yr

Demonstrated understanding of ISO-9001 Quality Management System * Excellent organizational skills and attention to detail. * Excellent time management and problem-solving skills. * Strong ...

Impact Housing

Quality Supervisor

Yorba Linda, CA · On-site

$80K - $85K/yr

Manage inspection plans, quality documentation, and non-conformance resolution. * Approve final ... ISO 9001 experience. * Bilingual English/Spanish. EDUCATION * Associate's Degree in Engineering or ...

Impact Housing

Quality Supervisor

Yorba Linda, CA · On-site

$85K - $90K/yr

Manage inspection plans, quality documentation, and non-conformance resolution. * Approve final ... ISO 9001 experience. * Bilingual English/Spanish. EDUCATION * Associate's Degree in Engineering or ...

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All JobsIso Quality JobsIso Quality Manager JobsIso Quality Manager Jobs in Riverside, CA

Iso Quality Manager information

See Riverside, CA salary details

$25K

$89.9K

$164.8K

How much do iso quality manager jobs pay per year?

As of Sep 9, 2026, the average yearly pay for iso quality manager in Riverside, CA is $89,887.00, according to ZipRecruiter salary data. Most workers in this role earn between $45,900.00 and $141,900.00 per year, depending on experience, location, and employer.

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.

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 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 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 popular job titles related to Iso Quality Manager jobs in Riverside, CA?

For Iso Quality Manager jobs in Riverside, CA, the most frequently searched job titles are:

What job categories do people searching Iso Quality Manager jobs in Riverside, CA look for?

The top searched job categories for Iso Quality Manager jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Iso Quality Manager jobs?

Cities near Riverside, CA with the most Iso Quality Manager job openings:

Iso Quality Manager jobs near you
Infographic showing various Iso Quality Manager job openings in Riverside, CA as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $89,887 per year, or $43.2 per hour.

Manager, Product Quality

Irvine, CA • On-site

Fortive
Electrical Equipment, Appliance, and Component Manufacturing • 5 - 10K employees
Learn more about Fortiveexternal

Full-time

Posted 28 days ago

Fortive rating

7.9

Company rating: 7.9 out of 10

Based on 9 frontline employees who took The Breakroom Quiz

Job description

Job Title 

Manager, Product Quality 

Job summary 

Leads a global team responsible for executing scalable product quality activities across design quality and customer quality. The role ensures high-quality, compliant, and efficient delivery of verification and validation activities, distributed product quality management, complaint intake, and quality data insights. 

Key Responsibilities 

Under minimal supervision, general direction, and in accordance with applicable government laws, regulations, and ASP policies, procedures, and guidelines, this position shall: 

- Lead, coach, and develop a team of product quality professionals to deliver high-quality execution across design and customer quality workstreams.   

- Manage software verification and validation (V&V) execution, ensuring compliant, complete, and scalable delivery aligned to design controls and product lifecycle requirements.   

- Manage complaint intake, support APAC complaint investigations, ensuring quality, timeliness, and escalation of emerging product risks.   

- Own the end-to-end product quality lifecycle for distributed products. 

- Develop and maintain product quality dashboards and reporting to enable data-driven decision making and visibility of product performance and risk signals.   

- Implement scalable operating mechanisms, including standard work, automation, risk-based work tiering, and structured QMS workshop/Kaizen activities to improve efficiency, strengthen compliance, and reduce the cost of poor quality. 

- Ensure compliance with quality system requirements and regulatory expectations, maintaining audit readiness and robust documentation practices.   

- Collaborate globally and cross-functionally with RAQA, R&D, IT, Operations, Manufacturing, Supplier Quality, and regional teams to ensure clear interfaces, effective handoffs, alignment on quality priorities, and sustained execution of improvement initiatives. 

Education and Experience Requirements 

- Bachelor's degree (or equivalent experience) in Engineering, Quality, Computer Science, Life Sciences, or related discipline.   

- Minimum 6 years of experience in Product Quality, Design Quality, Customer Quality, or related field within medical device industry.   

- Minimum 2 years of experience leading or supervising professional employees or teams. 

Role and Competencies Requirements 

- Demonstrated ability to lead and develop professional teams while driving accountability for results.   

- Strong working knowledge of design controls, verification and validation, complaint handling, and post-market quality processes.   

- Ability to apply risk-based thinking and problem-solving to operational and technical quality challenges.   

- Experience driving process standardization, continuous improvement, scalable operating models, QMS workshops, Kaizen events, standard work deployment, and sustainment of process improvements. 

- Data-driven mindset with ability to leverage analytics to identify trends, risks, and performance gaps.   

- Strong communication skills to convey expectations, escalate issues, and guide stakeholders. 

- Knowledge of 21 CFR Part 820, ISO 13485, and EU MDR. 

- Experience in quality systems within medical device, pharmaceutical, or other regulated industry. 

- Experience supporting regulatory compliance inspections and audits. 

- Process excellence tools/methodologies (Six Sigma, FBS, etc.). 

- Good working knowledge of several FBS tools. 

- Travel: Domestic and International. 

What Fortive employees say

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About Fortive

Sourced by ZipRecruiter

Fortive is a diversified technology company that operates across multiple industries, delivering innovative solutions and products that empower businesses to enhance their productivity and operational efficiency. With a strong portfolio of industry-leading brands, Fortive focuses on creating intelligent, connected devices and software that enable precise measurement, control, and optimization. Fortive's expertise spans various sectors, including industrial automation, transportation, healthcare, and retail. Through advanced technologies and solutions, Fortive help customers automate processes, improve quality and safety, and drive overall performance. Whether it's precision measurement instruments, sensing technologies, or software platforms, Fortive provides reliable and scalable solutions that meet the evolving needs of their customers.

Industry

Electrical equipment, appliance, and component manufacturing

Company size

5,001 - 10,000 Employees

Headquarters location

Everett, WA, US

Year founded

2016

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