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Quality Manager Medical Device Jobs in Riverside, CA

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Medical Device Assembler I - Irvine, CA Contract-to-Hire Pay: $19.00 to $21.50/hr DOE + shift ... Inspect work to ensure quality and accuracy. * Maintain a clean, organized, and safe work ...

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Medical Device Assembler, Weekend Day 3/12 Schedule

Irvine, CA · On-site

$19 - $20/hr

  • Medical

  • Dental

  • Vision

Medical Device implant manufacturer in Irvine is seeking applicants with manufacturing experience ... Demonstrate accuracy, thoroughness and monitors own work to ensure quality. * Practice and always ...

2nd Shift Assembler - Medical Device

Irvine, CA · On-site

$21 - $22.50/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Report quality or process issues * Maintain a clean and safe workspace * Support team training and ... medical device or cleanroom experience * Experience with catheters or similar components

... in medical device or contract manufacturing * Hands-on experience with cable and wire harness ... Experience managing nonconformances and CAPAs in a regulated environment * High school diploma or ...

Cybersecurity Quality Engineer

Irvine, CA

$85K - $105K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Cybersecurity Quality Engineer supports the integration of cybersecurity requirements into the product development lifecycle and quality management system for Masimo medical device products.

Cybersecurity Quality Engineer

Irvine, CA · On-site

$85K - $105K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Cybersecurity Quality Engineer supports the integration of cybersecurity requirements into the product development lifecycle and quality management system for Masimo medical device products.

Cybersecurity Quality Engineer

Irvine, CA · On-site

$85K - $105K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Cybersecurity Quality Engineer supports the integration of cybersecurity requirements into the product development lifecycle and quality management system for Masimo medical device products.

Job Title Manager, Product Quality Job summary Leads a global team responsible for executing ... medical device industry. - Minimum 2 years of experience leading or supervising professional ...

Showing results 21-40

Quality Manager Medical Device information

See Riverside, CA salary details

$25K

$89.9K

$164.8K

How much do quality manager medical device jobs pay per year?

As of Aug 19, 2026, the average yearly pay for quality manager medical device 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 a quality manager do in the medical device industry?

A Quality Manager in the medical device industry is responsible for ensuring that products meet all regulatory requirements and quality standards throughout their lifecycle. They develop, implement, and monitor quality management systems, oversee internal and external audits, and work closely with manufacturing, engineering, and regulatory teams to maintain compliance with standards such as ISO 13485 and FDA regulations. Their role is critical to ensuring patient safety and product efficacy by preventing defects and ensuring consistent quality.

What are the key skills and qualifications needed to thrive as a quality manager in the medical device industry?

To thrive as a Quality Manager in the Medical Device industry, you need a solid background in quality assurance, regulatory compliance (such as ISO 13485 and FDA 21 CFR Part 820), and process improvement, often supported by a relevant degree in engineering or life sciences. Familiarity with quality management systems (QMS), risk management tools (like FMEA), and certifications such as ASQ Certified Quality Auditor (CQA) or Six Sigma are typically required. Strong leadership, attention to detail, and effective communication are vital soft skills for managing teams and ensuring cross-functional alignment. These skills and qualifications are crucial to ensure product safety, regulatory compliance, and the overall success of medical device manufacturing and delivery.

What are some common challenges quality managers face when ensuring compliance in the medical device industry?

Quality Managers in the medical device industry often encounter challenges such as keeping up with evolving regulatory requirements (like FDA, ISO 13485, and MDR), coordinating cross-functional teams to maintain strict quality standards, and managing documentation for audits. They must also address nonconformities quickly and implement corrective and preventive actions to avoid product recalls. Effective communication and strong attention to detail are essential for navigating these challenges while maintaining product safety and regulatory compliance.

What is the difference between Quality Manager Medical Device vs Quality Engineer Medical Device?

AspectQuality Manager Medical DeviceQuality Engineer Medical Device
Primary FocusOversees quality systems, compliance, and team managementDesigns, develops, and implements quality testing and inspection processes
CertificationsISO 13485, Six Sigma, Lead AuditorISO 13485, Six Sigma, Certified Quality Engineer (CQE)
Work EnvironmentManagement, regulatory compliance, cross-department collaborationProduct testing, process improvement, technical analysis
Industry UsageUsed across organizations to ensure overall quality managementUsed in product development and testing phases

The main difference is that the Quality Manager Medical Device focuses on managing quality systems and compliance at a strategic level, while the Quality Engineer Medical Device concentrates on technical testing and process improvements. Both roles require similar certifications and work within the same industry but serve different functions within quality assurance.

What are popular job titles related to Quality Manager Medical Device jobs in Riverside, CA?

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

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

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

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

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

Infographic showing various Quality Manager Medical Device job openings in Riverside, CA as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 16% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $89,887 per year, or $43.2 per hour.

Senior Software Quality Engineer, Product/Software Cybersecurity (Medical Device Software)

Edwards Lifesciences Corporation

Irvine, CA • On-site

$108K - $153K/yr

Full-time

Re-posted 6 days ago


Edwards Lifesciences rating

8.3

Company rating: 8.3 out of 10

Based on 30 frontline employees who took The Breakroom Quiz

68th of 540 rated manufacturers


Job description

Imagine how your ideas and expertise can change a patient's life. Our Quality teams help shape the development of groundbreaking technologies to ensure each stage of our innovation process is held to the highest standards of integrity and safety. You'll bring your passion for problem solving and partner with various teams to influence decision-making for a product's entire lifecycle. Your work will involve you optimizing product development to impact patients around the world with pioneering technology.

The Senior Software Quality Engineer is a key member of the Software Quality organization, responsible for ensuring the cybersecurity of product software including Software as a Medical Device (SaMD), Software in a Medical Device (SiMD), software as an accessory to a medical device, and other Digital Health Technologies. This role is responsible for owning and advancing product cybersecurity processes established within our Quality Management System and ensure alignment with applicable regulatory standards and industry guidance. The position will work in close partnership with R&D, Product Security, Quality and other cross-functional team members to integrate cybersecurity requirements throughout the product software development lifecycle and support effective postmarket cybersecurity management.

We are seeking an ambitious, technically strong candidate with a solid foundation in quality and cybersecurity, excellent communication skills, and the ability to build trusted relationships across the organization. This role offers meaningful opportunities to grow within a dynamic and evolving Software Quality function.

How you will make an impact:

  • Own the establishment, implementation, and continuous improvement of cybersecurity related processes for product software established in our Quality Management System
  • Review and approve product cybersecurity related deliverables across the lifecycle, including planning, requirements, architecture/design, risk management, verification and validation, and problem resolution (dispositioning of cybersecurity vulnerabilities and defects).
  • Execute Cybersecurity risk analysis on our products.
  • Provide assurance that all requirements related to cybersecurity are followed when developing or making changes to product software.
  • Work in close partnership with Product Security, Quality and R&D to address and monitor cybersecurity risks throughout the Product Software Development Lifecycle.
  • Support regulatory submissions and responses regarding cybersecurity related requests.
  • Effectively manage multiple priorities, projects and ability to communicate at all levels of personnel.
  • Author, review and approve documents in our Application Lifecycle Management and Product Lifecycle Management systems.
  • Willingness to work in a fast-paced, dynamic environment to meet the needs of the business and deliver safe quality products to our patients.

What you will need (Required):

  • Bachelor's degree in Scientific, Engineering, or Computer Sciencefields plus four (4) years of relevant work experience; OR Master's degree Scientific, Engineering, or Computer Sciencefields plus two (2) years of relevant work experience; or equivalent work experience based on Edwards criteria .
  • Highly regulated industry experience
  • Experience with software development and/or software quality in regulated environments

What else we look for (Preferred):

  • Engineering or Computer Science degree
  • Medical device industry experience
  • Experience with cybersecurity risk assessments
  • Experience integrating cybersecurity into the SDLC / design controls
  • Familiarity with vulnerability management and post market cybersecurity processes
  • Familiarity withsoftware(IEC 62304) and cybersecurity (NIST)guidelines; includingunderstanding ofWaterfall and Agile conceptsin context with the SDLC process.
  • Knowledge and experience in Medical Device Risk Management (ISO 14971)
  • Excellent written and verbal communication skillsrequired.

Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
For California (CA), the base pay range for this position is $108,000 to $153,000 in tool (highly experienced).
The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.

Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.

COVID Vaccination Requirement

Edwards is committed to protecting our vulnerable patients and the healthcare providers who are treating them. As such, all patient-facing and in-hospital positions require COVID-19 vaccination. If hired into a covered role, as a condition of employment, you will be required to submit proof that you have been vaccinated for COVID-19, unless you request and are granted a medical or religious accommodation for exemption from the vaccination requirement. This vaccination requirement does not apply in locations where it is prohibited by law to impose vaccination.


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About Edwards Lifesciences

Sourced by ZipRecruiter

Edwards Lifesciences is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. Driven by a passion to help patients, the company collaborates with the world's leading clinicians and researchers to address unmet healthcare needs, working to improve patient outcomes and enhance lives. Headquartered in Irvine, California, Edwards Lifesciences has extensive operations in North America, Europe, Japan, Latin America and Asia and currently employs over 15,000 individuals worldwide. For us, helping patients is not a slogan - it's our life's work. From developing devices that replace or repair a diseased heart valve to creating new technologies that monitor vital signs in the critical care setting, we focus on helping patients regain and improve the quality of their life.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Irvine, CA, US

Year founded

1958