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Iso Manager Jobs in Riverside, CA (NOW HIRING)

ISO 13485 Quality Management Systems * Certified Lead Auditor or equivalent auditing certification. * Experience interacting with regulatory agencies or supporting regulatory inspections. Preferred ...

ISO 13485 Quality Management Systems * Certified Lead Auditor or equivalent auditing certification. * Experience interacting with regulatory agencies or supporting regulatory inspections. Preferred ...

Plans, implements, and directs quality program consistent with ISO and AS9100 quality systems ... Manages the process integrity/data collection processes and reporting to senior management.

Plans, implements, and directs quality program consistent with ISO and AS9100 quality systems ... Manages the process integrity/data collection processes and reporting to senior management.

Plans, implements, and directs quality program consistent with ISO and AS9100 quality systems ... Manages the process integrity/data collection processes and reporting to senior management.

... including ISO/TS 16949 and ISO 14001 certifications. Product Manager We're hiring a hands-on ... Product Manager to own and drive key product lines across OEM, OES, and aftermarket channels. This ...

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Iso Manager information

See Riverside, CA salary details

$28.7K

$85.2K

$143.4K

How much do iso manager jobs pay per year?

As of Jul 13, 2026, the average yearly pay for iso manager in Riverside, CA is $85,210.00, according to ZipRecruiter salary data. Most workers in this role earn between $52,200.00 and $121,500.00 per year, depending on experience, location, and employer.

What are some common challenges faced by ISO Managers when implementing new quality management systems, and how can they be overcome?

ISO Managers often encounter resistance to change from staff when introducing new quality management systems, as well as difficulties in aligning existing processes with ISO standards. To overcome these challenges, it's important to foster open communication, provide thorough training, and involve team members early in the process. Additionally, collaborating closely with department heads helps ensure that each area understands the benefits and requirements of compliance, making the transition smoother and more sustainable.

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

AspectIso ManagerQuality Assurance Specialist
CertificationsISO Lead Auditor, ISO 9001/14001/45001 certificationsISO 9001 Internal Auditor, CQE, CQA certifications
Work EnvironmentManufacturing, industrial, corporate quality departmentsManufacturing, service, healthcare sectors
Employer & Industry UsageCompanies implementing ISO standards, compliance teamsOrganizations focusing on quality control, process improvement

While both roles focus on quality and standards, the Iso Manager primarily oversees ISO compliance and certification processes, ensuring organizational adherence to international standards. The Quality Assurance Specialist concentrates on product quality, testing, and process improvements within various industries. Understanding these differences helps in selecting the right career path or job role based on your expertise and industry focus.

What is ISO job description?

An ISO Manager is responsible for developing, implementing, and maintaining an organization's ISO management systems, such as ISO 9001 or ISO 14001. They ensure compliance with international standards, conduct audits, and facilitate continuous improvement processes, often requiring knowledge of quality management tools and certification procedures.

What is an ISO Manager?

An ISO Manager is a professional responsible for overseeing the implementation and maintenance of ISO (International Organization for Standardization) standards within an organization. Their primary duties include ensuring compliance with relevant ISO standards, conducting internal audits, and leading the process for certification or recertification. ISO Managers work to improve organizational processes, train staff on quality management systems, and liaise with external auditors. They play a crucial role in helping organizations achieve and maintain high standards of quality, safety, and efficiency.

What is ISO management?

ISO management refers to the implementation and oversight of processes aligned with ISO standards, such as ISO 9001 for quality management. An ISO manager ensures compliance, maintains documentation, and facilitates continuous improvement within an organization to meet international standards.

What is an ISO relationship manager?

An ISO (Independent Sales Organization) relationship manager is responsible for building and maintaining partnerships with ISO agents or sales organizations that resell payment processing services. They coordinate sales efforts, provide support, and ensure compliance with industry standards, often using CRM tools and industry certifications to manage relationships effectively.

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

To thrive as an ISO Manager, you need in-depth knowledge of ISO standards (such as ISO 9001, 14001, or 27001), quality management principles, and relevant industry regulations, usually backed by a degree in a related field and ISO Lead Auditor certification. Familiarity with audit management tools, document control systems, and compliance software is typically required. Strong analytical thinking, attention to detail, and effective communication skills help in leading teams, facilitating audits, and driving continuous improvement. These skills ensure robust compliance, foster a culture of quality, and help organizations maintain certifications critical for credibility and operational excellence.

What is the role of an ISO manager?

An ISO manager is responsible for developing, implementing, and maintaining an organization's ISO management systems to ensure compliance with international standards such as ISO 9001 or ISO 14001. They conduct audits, oversee process improvements, and ensure staff adherence to quality or environmental protocols, often requiring certification and strong organizational skills.
What are popular job titles related to Iso Manager jobs in Riverside, CA? For Iso Manager jobs in Riverside, CA, the most frequently searched job titles are:
What job categories do people searching Iso Manager jobs in Riverside, CA look for? The top searched job categories for Iso Manager jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Iso Manager jobs? Cities near Riverside, CA with the most Iso Manager job openings:
Manager, Product Safety Risk Management

Manager, Product Safety Risk Management

JenaValve

Irvine, CA โ€ข On-site

$138K/yr

Full-time

Posted 7 hours ago


Job description

Job Title: Manager, Product Safety Risk Management
Role Level: Individual Contributor
Supervisor/Manager Title: Vice President Quality and Compliance
Job Location & Environment: Irvine, CA- Corporate Office
Job Description Summary: Manager, Product Safety Risk Management is responsible for leading and advancing product safety risk management across JenaValve's product portfolio, ensuring a consistent, compliant, and risk-based approach from concept through post-market surveillance. This role supports the product safety risk management framework and governance model, helping to drive clear, timely, and well-supported decisions across programs in alignment with ISO 14971, applicable regulatory requirements, design controls, usability engineering, and process risk management.
The Manager serves as a subject matter expert for complex product safety decisions, partners closely with cross-functional stakeholders, and contributes to audits, inspections, and regulatory interactions related to product safety. This is a manager-level individual contributor role with the opportunity to build team leadership responsibilities over time. Success in this role is reflected in effective detection and response to emerging post-market safety signals, strong quality of risk-based decisions, robust risk assessments during product development, and sustained inspection readiness.
Job Responsibilities:
  • Leads execution of the product safety risk management framework and governance model, ensuring consistent application of ISO 14971-aligned practices across the portfolio and throughout the product lifecycle.
  • Develops, implements, and continuously improves policies, procedures, templates, tools, and quality system controls that enable effective and scalable product safety risk management.
  • Provides product safety risk management leadership for complex programs, supporting cross-functional teams with timely, risk-based decision making, escalation, and resolution.
  • Ensures product safety risk management is integrated with design controls, software development lifecycles, usability engineering, process risk management, verification and validation, and post-market surveillance.
  • Oversees the quality and completeness of risk management files and related documentation, including hazard analyses, FMEAs, fault tree analyses, benefit-risk analyses, residual risk evaluations, and Health Hazard Evaluations.
  • Leads post-market safety activities, including safety signal assessment, Health Hazard Evaluations, CAPAs, and cross-functional response planning, to support effective monitoring of product risk performance.
  • Contributes product safety risk management content for regulatory submissions, design changes, and product lifecycle assessments.
  • Partners in audits, inspections, and regulatory interactions related to product safety, helping ensure sustained inspection readiness and effective response to findings and inquiries.
  • Establishes and monitors meaningful metrics to assess the effectiveness of product safety risk management processes and product performance.
  • Promotes a culture of patient safety, accountability, and continuous improvement.

Required Education and Experience:
  • 8-10 years of progressive experience in medical device or healthcare technology, including significant responsibility for product safety risk management in regulated environments.
  • Demonstrated expertise applying ISO 14971 across pre-market and post-market phases, including experience with risk management processes and governance.
  • Strong understanding of design controls and their integration with usability engineering, and post-market surveillance.
  • Proven ability to influence senior stakeholders, lead cross-functional decision making, and communicate complex risk issues with clarity and judgment.
  • Experience leading initiatives or mentoring others in product safety risk management or closely related quality and regulatory functions is preferred.

Skills and Abilities Required for This Job:
  • Advanced knowledge of applicable standards and regulations, including ISO 13485, 21 CFR Part 820, and EU MDR 2017/745.
  • Strong working knowledge of risk management methods and deliverables, including hazard analysis, FMEA, fault tree analysis, benefit-risk analysis, and residual risk evaluation.
  • Experience with quality systems, product development processes, and enabling technologies or work management platforms that support product lifecycle and risk management activities.

Leadership Competencies
  • Exercises sound judgment and operate effectively with a high degree of independence in a complex environment.
  • Drives accountability, collaboration, and continuous improvement across functions while maintaining a strong focus on patient safety and product quality.
  • Demonstrates leadership through influence, partnership, and effective communication across levels of the organization.

Physical Requirements:
  • Travel domestic and international up to10% time.