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Remote Medical Device Quality Assurance Jobs in Riverside, CA

EDI Developer

Rancho Santa Margarita, CA · On-site +1

$90K - $140K/yr

  • Medical

  • Life

  • Retirement

  • PTO

Applied Medical is a new generation medical device company with a proven business model and ... Our unique business model, combined with our dedication to delivering the highest quality products ...

EDI Developer

Rancho Santa Margarita, CA · On-site +1

$90K - $140K/yr

  • Medical

  • Life

  • Retirement

  • PTO

Applied Medical is a new generation medical device company with a proven business model and ... Our unique business model, combined with our dedication to delivering the highest quality products ...

Assessment Property Condition Reviewer

Irvine, CA · Remote

$85K - $110K/yr

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

This role is typically fulfilled as a remote employee. If a proximate NV5 office and space are ... Perform quality assurance (QA) and quality control (QC) reviews of commercial Property and Facility ...

Assessment Property Condition Reviewer

Irvine, CA · On-site +1

$85K - $110K/yr

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

This role is typically fulfilled as a remote employee. If a proximate NV5 office and space are ... Perform quality assurance (QA) and quality control (QC) reviews of commercial Property and Facility ...

Showing results 41-60

Remote Medical Device Quality Assurance information

See Riverside, CA salary details

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$64

How much do remote medical device quality assurance jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for remote medical device quality assurance in Riverside, CA is $30.56, according to ZipRecruiter salary data. Most workers in this role earn between $19.57 and $35.87 per hour, depending on experience, location, and employer.

What is remote medical device quality assurance?

Remote Medical Device Quality Assurance involves ensuring that medical devices meet regulatory and quality standards while working from a location outside of a traditional office or laboratory. Professionals in this role review documentation, conduct virtual audits, and collaborate with teams to maintain compliance with industry regulations such as FDA or ISO standards. The work helps ensure patient safety and product effectiveness, even when performed remotely, by leveraging digital tools and secure communication platforms. This role is essential for companies manufacturing medical devices, as it helps identify and mitigate risks throughout the product lifecycle.

What are the key skills and qualifications needed to thrive as a remote medical device quality assurance professional?

To thrive as a Remote Medical Device Quality Assurance professional, you need a solid understanding of quality management systems, regulatory compliance (such as FDA and ISO 13485), and experience in medical device manufacturing or engineering. Familiarity with tools like CAPA systems, document control software, and audit management platforms, along with relevant certifications such as CQE or RAC, is highly valuable. Strong attention to detail, analytical thinking, and effective remote communication skills help you excel in ensuring product quality and regulatory adherence. These competencies are crucial for maintaining safety standards, ensuring compliance, and supporting product integrity in a distributed work environment.

How does a remote medical device quality assurance professional typically collaborate with cross-functional teams to ensure compliance and product quality?

In a remote Medical Device Quality Assurance role, professionals regularly work with cross-functional teams such as engineering, regulatory affairs, and manufacturing via virtual meetings and digital collaboration tools. They participate in design reviews, risk assessments, and audits to ensure that all processes and products meet regulatory standards. Clear communication, thorough documentation, and proactive follow-up are essential to bridge the distance and keep projects on track. Adapting to virtual teamwork and leveraging technology are key to maintaining high standards in product quality and compliance.

What is the difference between Remote Medical Device Quality Assurance vs Remote Medical Device Regulatory Affairs Specialist?

AspectRemote Medical Device Quality AssuranceRemote Medical Device Regulatory Affairs Specialist
CertificationsISO 13485, FDA QSR, CAPAFDA, ISO 13485, Regulatory Affairs certifications
Work EnvironmentQuality departments, manufacturing, compliance teamsRegulatory teams, legal, compliance departments
Industry UsageEnsures product quality, compliance, auditsManages submissions, regulatory strategies, approvals
Search IntentQuality assurance roles, compliance jobsRegulatory affairs roles, submission jobs

Remote Medical Device Quality Assurance focuses on maintaining product quality, compliance, and conducting audits, while Remote Medical Device Regulatory Affairs Specialists handle regulatory submissions, approvals, and compliance strategies. Both roles are essential in the medical device industry but serve different functions within the product lifecycle.

What are the most commonly searched types of Medical Device Quality Assurance jobs in Riverside, CA?

The most popular types of Medical Device Quality Assurance jobs in Riverside, CA are:

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

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

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

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

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

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

Clinical Trial Psych Rater - German Speaking

IQVIA

Moreno Valley, CA • Remote

Part-time

Posted 25 days ago


IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

62nd of 224 rated it services


Job description

Clinical Trial Psych Rater - German Speaking

Location: Remote/Virtual
Hours: Estimated 10-16 hours per month
Role: Clinical Specialist

About IQVIA

IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world's leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials.

Position Overview

The Clinical Specialist plays a key role in ensuring the integrity and reliability of clinical trial data. This position involves reviewing scales administered by raters to confirm standardized assessment practices. Responsibilities include evaluating assessment quality, engaging in live discussions with raters to provide guidance on methodology and scoring techniques, and supporting rater performance through functional assessments (e.g., mock interviews). Additional tasks may include assisting with communication materials and documentation.

Key Responsibilities

  • Participate in all required orientation, training, and calibration activities.

  • Review case data and prepare for rater discussions, ensuring all relevant documents and scale items are available.

  • Conduct live interactions with raters to provide feedback and guidance on assessment methodology and scoring.

  • Complete assigned tasks and rater interactions according to schedule.

  • Submit all required documentation accurately and on time.

Required Qualifications

  • Education: Master's degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work (or equivalent). MD, DO, or PhD preferred.

  • Experience:

    • Minimum 3 years administering psychiatric assessments, rating scales, and/or structured clinical interviews (specifically MINI; MADRS; CAPS; PCL-5; CSSRS; CGI: OR MINI; PANSS; AIMS; BARS; LSAS; PGI-S)

    • Minimum 3 years of clinical experience with psychiatric populations.

    • Minimum 3 years administering scales in clinical research trials (excluding graduate/doctoral research).

    • Experience in CNS trials preferred.

  • Skills:

    • Strong interpersonal and communication skills for professional interaction at all levels.

    • Excellent organizational skills, attention to detail, time management, and problem-solving ability.

    • Proficiency with Windows and Microsoft Office applications.

Language Requirement

Current openings require fluency in English and native-level proficiency in German.

#LI-DNP #LI-Remote #LI-HCPN

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.


What IQVIA employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


IQVIA logo

About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US