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Remote Gcp Qa Jobs (NOW HIRING)

Minimum Experience: * 2 years of experience in Quality Assurance * 4 years of experience in Clinical Research working in a compliance or GCP relevant role How We Work Together * Location : Remote ...

Minimum Experience: * 2 years of experience in Quality Assurance * 4 years of experience in Clinical Research working in a compliance or GCP relevant role How We Work Together * Location : Remote ...

Senior GCP Auditor

$82K - $101K/yr

Participate in solving GCP compliance issues within Quality Assurance, Clinical Operations ... This position works remote * Flexibility in working schedule, i.e., off-hours, second shift ...

We seek a Lead Quality Assurance Engineer for an exciting remote opportunity based in Miami. Our ... Experience with test environments in cloud platforms (AWS/GCP/Azure) Our client's team works in a ...

Remote working What You'll Be Doing * Serve as the primary Quality Assurance liaison for the ... Extensive knowledge of global GxP regulations and standards, including Good Clinical Practice (GCP ...

Remote working What You'll Be Doing * Serve as the primary Quality Assurance liaison for the ... Extensive knowledge of global GxP regulations and standards, including Good Clinical Practice (GCP ...

JOB OVERVIEW: We are looking for a Lead Quality Assurance Engineer for an exciting remote ... Experience with test environments in cloud platforms (AWS/GCP/Azure) Our client's team works in a ...

JOB OVERVIEW: We are looking for a Lead Quality Assurance Engineer for an exciting remote ... Experience with test environments in cloud platforms (AWS/GCP/Azure) Our client's team works in a ...

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Remote Gcp Qa information

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How much do remote gcp qa jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for remote gcp qa in the United States is $31.91, according to ZipRecruiter salary data. Most workers in this role earn between $18.75 and $34.86 per hour, depending on experience, location, and employer.

What is a Remote GCP QA?

A Remote GCP QA (Google Cloud Platform Quality Assurance) professional is responsible for testing and ensuring the quality of applications and services deployed on Google Cloud, while working remotely. Their tasks include creating and executing test plans, identifying bugs, and verifying that cloud-based systems meet required performance and security standards. They collaborate with developers, cloud engineers, and other stakeholders to deliver reliable, scalable solutions. Remote GCP QAs leverage their expertise in both software testing and cloud technologies to support development teams from any location.

What are the key skills and qualifications needed to thrive as a Remote GCP QA, and why are they important?

To thrive as a Remote GCP QA, you need a strong background in software testing, cloud computing concepts, and quality assurance methodologies, often backed by a degree in computer science or a related field. Proficiency with Google Cloud Platform (GCP) tools, automated testing frameworks like Selenium or JUnit, and certifications such as Google Associate Cloud Engineer are typically required. Excellent problem-solving, attention to detail, and effective remote communication skills set outstanding candidates apart. These competencies are crucial for ensuring high-quality, secure, and reliable cloud-based applications while collaborating efficiently in distributed teams.

How does a Remote GCP QA collaborate with development and operations teams despite working remotely?

As a Remote GCP QA, collaboration with development and operations teams is primarily facilitated through cloud-based tools, regular video meetings, and shared documentation platforms. You’ll often participate in daily stand-ups, sprint planning sessions, and bug triage meetings to ensure smooth communication across time zones. Effective remote QAs proactively communicate test results, clarify requirements, and provide feedback to developers, while also coordinating with DevOps to integrate automated tests within CI/CD pipelines. Building strong relationships and maintaining transparency are key to overcoming the challenges of remote work in this role.

What is the difference between Remote Gcp Qa vs Remote Cloud Data Engineer?

AspectRemote Gcp QaRemote Cloud Data Engineer
CertificationsGCP Professional Cloud Architect, GCP Professional Data EngineerGCP Professional Data Engineer, Big Data certifications
Work EnvironmentRemote, collaborative with development and testing teamsRemote, data pipeline and infrastructure focus
Industry UsageSoftware testing, quality assurance in cloud appsData processing, analytics, cloud infrastructure

Remote Gcp Qa specialists focus on testing and quality assurance of cloud-based applications on GCP, ensuring functionality and performance. Remote Cloud Data Engineers build and maintain data pipelines and infrastructure on GCP. While both roles require GCP certifications and often work remotely, Gcp Qas concentrate on testing, whereas Data Engineers focus on data architecture and processing.

What cities are hiring for Remote Gcp Qa jobs?

Cities with the most Remote Gcp Qa job openings:

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

The most popular types of Gcp Qa jobs are:

What states have the most Remote Gcp Qa jobs?

States with the most job openings for Remote Gcp Qa jobs include:

What are popular job titles related to Remote Gcp Qa jobs?

For Remote Gcp Qa jobs, the most frequently searched job titles are:

Infographic showing various Remote Gcp Qa job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 88% Full Time, 4% Part Time, 5% Contract, and 1% Nights. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $66,371 per year, or $31.9 per hour.

Specialist, Quality Assurance

OR • On-site, Remote

Care Access
Scientific Research and Development Services • 501 - 1,000 employees

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 3 days ago


Job description

How This Role Makes a Difference

Care Access is seeking a dedicated, experienced, and innovation-driven Quality Assurance Specialist (GxP) to support the success of the Quality Assurance Department and organizational compliance activities. The Quality Assurance Specialist will be responsible for closely monitoring the quality and compliance of clinical work at both traditional trial sites and decentralized trials. The QA specialist will directly support quality initiatives, audit functions, CAPA systems and promote inspections readiness.  Working in support of the Associate Director of Quality Assurance, the Quality Assurance Specialist will ensure that Care Access maintains a high level of quality while executing clinical trials according to Care Access SOPs, GCP, and FDA/ICH Guidelines.

How You'll Make An Impact
  • Site-Level Quality & Data Integrity: Ensure the highest standards of patient safety and data integrity at clinical research sites through regular quality assurance reviews, interpreting and implementing standard QA procedures. 
  • GCP Regulatory Document Review: Conduct comprehensive reviews of study-specific regulatory binders and clinical documents to verify they are accurately completed, submitted, and maintained per GCP standards. 
  • Audit Execution & Tracking: Execute the yearly corporate audit plan, systematically tracking quality assurance audits, monitoring related activities, and preparing detailed outcome reports for management. 
  • Issue Resolution & CAPA Management: Partner directly with research staff and Principal Investigators (PIs) to resolve identified compliance issues, developing, tracking, and monitoring Corrective and Preventative Action (CAPA) plans. 
  • External Audit & Inspection Support: Coordinate and provide hands-on operational support for on-site audits and inspections conducted by external providers, sponsors, and regulatory agencies. 
  • Quality Systems Administration: Provide ongoing administrative support to the Quality Department by maintaining internal quality systems, compliance trackers, and operational programs. 
  • SOP Development & Maintenance: Participate in the routine review, drafting, and maintenance of quality assurance Standard Operating Procedures (SOPs) to ensure alignment with evolving regulations. 
  • Cross-Functional Compliance Advisory: Act as an internal quality resource to provide ongoing guidance and best-practice recommendations to site personnel and clinical project teams. 
  • Regulatory compliance: be knowledgeable of evolving GxP guidelines. Ability to critically think, eagerness to learn, and commitment to ensuring compliance. Knowledge of and able to interpret regulatory guidance's such as 21 CFR Part 11/ Part 312, ICH GCP E6 (R3).  
  •  Inspection readiness: promote a culture of inspections readiness and continuous improvement. Be flexible to work with risk-based audit agendas and shifting priorities.  
  • Create and deliver training on Quality and Improvement activities  
  • Support completion of RFP/RFI (Request for proposals/information) 
  • Willingness to learn and engage with digital technologies  
  • Provide AI project quality support and consultation 
  • Support other activities related to the management of QMS and accuracy of data 
  • Support GxP and non GxP quality issues and/or projects needing quality consultation and support   
The Expertise Required 
  • Excellent working knowledge of medical and research terminology 
  • Excellent working knowledge of federal regulations and good clinical practices (GCP) 
  • Attention to detail 
  • Ability to communicate and work effectively with a diverse team of professionals 
  • Strong Organizational Skills: Able to prioritize, delegate, direct, support and evaluate others' work and follow through on assignments 
  • Communication Skills: Strong verbal and written communication skills as evidenced by positive interactions with coworkers, management, clients and vendors 
  • Team Collaboration Skills: Work effectively and collaboratively with other team members to accomplish mutual goals. Bring a positive and supportive attitude to achieving these goals 
  • Strong computer skills with demonstrated abilities using clinical trials database, IVR systems, electronic data capture, MS word and excel Ability to balance tasks with competing priorities 
  • Demonstrate decision making skills Curiosity and passion to learn, innovate, able to communicate any possible risks and get things done 
  • Friendly, outgoing personality with the ability to maintain a positive attitude under pressure 
  • High level of self-motivation and energy 
  • Ability to work independently in a fast-paced environment with minimal supervision 
  • Must have a client service mentality 
  • Experience with supporting multiple sites and identifying gaps 
  • Experience with internal and external audits: FDA, GCP, SOPs 
Certifications/Licenses, Education, and Experience
  • Minimum Education:
    • Bachelor's degree  
  • Minimum Experience:
    • 2 years of experience in Quality Assurance 
    • 4 years of experience in Clinical Research working in a compliance or GCP relevant role  
How We Work Together
  • Location: Remote within the United States. This role requires 100% of work to be performed in a remote office environment.
  • Travel: This is a remote position with up to 35% travel requirements. Must have the ability to travel. International travel may also be required as part of the role. 
  • Physical demands associated with this position Include: The ability to use keyboards and other computer equipment.

The expected pay range for this role is $70,000 - $90,000 USD per year for full time team members.

Benefits & Perks (US Full Time Employees)
  • Paid Time Off (PTO) and Company Paid Holidays
  • 100% Employer paid medical, dental, and vision insurance plan options
  • Health Savings Account and Flexible Spending Accounts
  • Bi-weekly HSA employer contribution
  • Company paid Short-Term Disability and Long-Term Disability
  • 401(k) Retirement Plan, with Company Match 
 
Mandatory Employer Disclosures
Notice to Illinois applicants: Applicants are not obligated to disclose expunged juvenile records or adjudication, arrest, or conviction.
Notice to Connecticut applicants: Care Access may require applicants to submit to a urinalysis drug test in connection with an application for employment.
Notice to Arizona, Georgia, Indiana, and North Dakota applicants: Care Access complies with applicable laws prohibiting smoking in and around places of employment.
Notice to Massachusetts applicants: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Notice to Rhode Island applicants: Care Access complies with Rhode Island law prohibiting smoking in enclosed areas within places of employment. Care Access is also subject to is subject to Chapters 29-38 of Title 28 of the Rhode Island General Laws.
Notice to Maryland applicants: UNDER MARYLAND LAW, AN EMPLOYER MAY NOT REQUIRE OR DEMAND, AS A CONDITION OF EMPLOYMENT, PROSPECTIVE EMPLOYMENT, OR CONTINUED EMPLOYMENT, THAT AN INDIVIDUAL SUBMIT TO OR TAKE A LIE DETECTOR OR SIMILAR TEST. AN EMPLOYER WHO VIOLATES THIS LAW IS GUILTY OF A MISDEMEANOR AND SUBJECT TO A FINE NOT EXCEEDING $100. 

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