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Temp Quality Engineer Medical Device Jobs in Riverside, CA

Masimo

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.

Aerotek

Medical Device Solderer

Irvine, CA

$22 - $25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Assemble catheters under a microscope, ensuring accuracy, consistency, and product quality ... If eligible, the benefits available for this temporary role may include the following: * Medical ...

Balda C Brewer

Principal Quality Engineer

Ontario, CA · On-site

$120K - $150K/yr

Minimum of 8 years of quality engineering experience in the medical device or combination product industry, with significant focus on medical device design and assembly process development. * Proven ...

BALT Group

Quality System Engineer II

Irvine, CA · On-site

This Quality Engineer will be expected to work directly with different functions while receiving ... Job Responsibilities Knowledge of quality systems for medical device manufacturing and requirements ...

BALT Group

Quality System Engineer II

Irvine, CA · On-site

This Quality Engineer will be expected to work directly with different functions while receiving ... Job Responsibilities Knowledge of quality systems for medical device manufacturing and requirements ...

OrthAlign Inc.

Supplier Quality Engineer

Irvine, CA · On-site

OrthAlign, Inc., a Smart Technology, growing medical device company, has an immediate opening for ... Maintain supplier quality records. You need: * Your BA/BS Engineering-oriented degree and 2+ years ...

Aerotek

Medical Device Assembler

Irvine, CA

$19 - $23.25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

You will work with microscopes and small components to produce high-quality products that support ... If eligible, the benefits available for this temporary role may include the following: * Medical ...

Australia-Employment

Quality Engineer

Irvine, CA · On-site

$90 - $100/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Quality Engineer $90,000 - $100,000 per year | Irvine, CA | On‑Site | Permanent Overview We are ... Experience in regulated industries (medical device, aerospace, defense) * Familiarity with ERP/MES ...

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Marquee Staffing - CB

Be Seen First

Medical Device Assemblers Cleanroom - 4/10's Schedule!!

Irvine, CA · On-site

$19 - $21/hr

  • Medical

  • Dental

  • Vision

Inspect work to ensure quality and accuracy. * Maintain a clean, organized, and safe work ... Each branch is full-service, providing temporary, contract, contract-to-hire and direct placement ...

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Showing results 21-40

All JobsQuality Engineer Medical Device JobsTemp Quality Engineer Medical Device JobsTemp Quality Engineer Medical Device Jobs in Riverside, CA

Temp Quality Engineer Medical Device information

See Riverside, CA salary details

$46.9K

$87.7K

$124.1K

How much do temp quality engineer medical device jobs pay per year?

As of Aug 19, 2026, the average yearly pay for temp quality engineer medical device in Riverside, CA is $87,675.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,100.00 and $97,000.00 per year, depending on experience, location, and employer.

What is the difference between Temp Quality Engineer Medical Device vs Temp Quality Technician Medical Device?

AspectTemp Quality Engineer Medical DeviceTemp Quality Technician Medical Device
CredentialsBachelor's in Engineering, Quality or related field; certifications like CQE often preferredHigh school diploma or associate degree; technical certifications beneficial
Work EnvironmentDesign, develop, and improve quality systems; collaborate with engineering teamsPerform inspections, testing, and documentation; support quality assurance processes
Employer & Industry UsageUsed in medical device manufacturing companies for process developmentCommonly employed in quality control labs and manufacturing lines

The Temp Quality Engineer Medical Device focuses on developing and improving quality systems, requiring more technical expertise and engineering knowledge. In contrast, the Temp Quality Technician Medical Device primarily handles testing, inspections, and documentation tasks. Both roles are essential in ensuring product quality but differ in responsibilities and required qualifications.

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

Edwards Lifesciences Corporation

Irvine, CA • On-site

$108K - $153K/yr

Full-time

Re-posted 4 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 Science fields plus four (4) years of relevant work experience; OR Master's degree Scientific, Engineering, or Computer Science fields 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 with software (IEC 62304) and cybersecurity (NIST) guidelines; including understanding of Waterfall and Agile concepts in context with the SDLC process.
  • Knowledge and experience in Medical Device Risk Management (ISO 14971)
  • Excellent written and verbal communication skills required.

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

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