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Freelance Qualcomm Qa Jobs (NOW HIRING)

Freelance Contract * Pay Rate: $15/hour What You'll Do * Review, evaluate, and annotate AI ... Experience in annotation, content review, quality assurance, data labeling, localization, or ...

Oversee quality assurance throughout the website development and content creation process ... This is a long term freelance role- possible Temp to Perm * Deep understanding of Social Media ...

Oversee quality assurance throughout the website development and content creation process ... This is a long term freelance role- possible Temp to Perm * Deep understanding of Social Media ...

Overview We're looking for freelance Creative Technologists to help push the studio's work forward ... and QA * A commitment to staying current with modern development tools and workflows, including ...

You balance workloads in various stages of a project - concept, design development, production and QA/deployment. Sometimes your focus is on high level conceptual design; at later project stages you ...

You balance workloads in various stages of a project - concept, design development, production and QA/deployment. Sometimes your focus is on high level conceptual design; at later project stages you ...

Our growing Paid Media team has an immediate opening for a Paid Media Strategist (Freelance) to ... Own all setup and QA including targeting, UTMs, pixels, creative delivery, and pacing checks ...

Our growing Paid Media team has an immediate opening for a Paid Media Strategist (Freelance) to ... Own all setup and QA including targeting, UTMs, pixels, creative delivery, and pacing checks ...

You balance workloads in various stages of a project - concept, design development, production and QA/deployment. Sometimes your focus is on high level conceptual design; at later project stages you ...

Overview We're looking for freelance Creative Technologists to help push the studio's work forward ... and QA * A commitment to staying current with modern development tools and workflows, including ...

Reviewing edits for quality assurance. * Organizing production assets and coordinating with producers and freelancers. * Supporting media studio operations and other production needs. Qualifications:

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How much do freelance qualcomm qa jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for freelance qualcomm qa in the United States is $22.83, according to ZipRecruiter salary data. Most workers in this role earn between $17.55 and $25.72 per hour, depending on experience, location, and employer.

What is the difference between Freelance Qualcomm Qa vs Freelance Qualcomm Software Engineer?

AspectFreelance Qualcomm QaFreelance Qualcomm Software Engineer
CredentialsQuality assurance certifications, technical testing skillsSoftware development degrees, coding certifications
Work EnvironmentTesting labs, remote testing setupsDevelopment teams, remote or on-site coding environments
Industry UsageFocus on product quality, testing Qualcomm hardware/softwareFocus on software development, coding, and system design

Freelance Qualcomm Qa professionals primarily focus on testing and quality assurance of Qualcomm products, ensuring functionality and reliability. In contrast, Freelance Qualcomm Software Engineers develop and implement software solutions for Qualcomm devices. While both roles require technical expertise, QA specialists concentrate on testing processes, whereas software engineers are involved in coding and system development.

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What are the most commonly searched types of Qualcomm Qa jobs?

The most popular types of Qualcomm Qa jobs are:

Infographic showing various Freelance Qualcomm Qa job openings in the United States as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 87% Full Time, 3% Part Time, 7% Contract, and 1% Nights. Highlights an 88% Physical, 4% Hybrid, and 8% Remote job distribution, with an average salary of $47,496 per year, or $22.8 per hour.

Pharmaceutical Quality GVP Auditors Freelance/Independent (Consulting)

Advarra

Remote

Part-time

Re-posted 9 days ago


Job description

If you're not already part of our Network, please register using the Expert Enrollment Form. https://advarra.my.site.com/experts/s/ Registration is required to be considered.
If you are in our network DO NOT fill out this form or click on the link.
Location
This role is open to candidates based in North America.
Company Information
At Advarra, we seek to foster an inclusive and collaborative environment where everyone is treated with respect and diverse perspectives are embraced. Treating one another, our clients, and clinical trial participants with empathy and care are key tenets of our culture at Advarra; we are committed to creating a workplace where each person is not only valued but empowered to thrive and make a meaningful impact.
Company Culture
Our people--both employees and consultants-are the heart of Advarra. They are the key to our success and the driving force behind our mission and vision. Our values (Patient-Centric, Ethical, Quality Focused, Collaborative) guide our actions and decisions. Knowing the impact of our work on trial participants and patients, we act with urgency and purpose to advance clinical research so that people can live happier, healthier lives.
Job Overview Summary
Advarra is seeking Good Pharmacovigilance Practice (GVP) Auditors to join our consultant network for North America -based projects. Auditors support compliance reviews across GVP clinical sites and vendors.
Job Duties & Responsibilities
  • Conduct Good Pharmacovigilance Practice (GVP) audits (planning, agenda, physical or remote audit, and report writing)
  • Evaluate investigator sites, CROs, and vendor compliance or qualification.
  • Prepare comprehensive audit reports detailing findings and root-causes.
  • Provide written audit reports in English.
  • If required will provide corrective actions support and present findings to QA leadership and stakeholders
  • Work collaboratively with clients to ensure quality standards.

Basic Qualifications
  • Minimum 10+ years of Clinical Quality Assurance and/or Good Pharmacovigilance Practice (GVP) experience.
  • Minimum 5+ years of Good Clinical Practices auditing experience.
  • Demonstrated experience with regulatory agency expectations (e.g., FDA, EMA) and audit readiness activities.
  • Demonstrated experience in developing and implementing quality assurance plans, audit programs, and corrective action plans.
  • Fluent English communication, verbal and written
  • Bachelor's degree

Preferred Qualifications
  • Strong interpersonal and client interaction skills.
  • Excellent analytical, problem-solving, communication, and report-writing skills.
  • Ability to work collaboratively across departments and interact with internal and external stakeholders.

Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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About Advarra

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

201 - 500 Employees

Headquarters location

Columbia, MD, US

Year founded

1983

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