ZipRecruiter

Log In

2

Remote Gcp Qa Jobs (NOW HIRING)

Sobi

QA Manager, GCP

San Diego, CA · On-site +1

$112K - $153K/yr

Ensuring quality oversight and quality assurance and quality by design activities related to GCP/GCLP area * Guide and support from a quality perspective the GCP/GCLP and GPP related activities ...

Sobi

QA Manager, GCP

Raleigh, NC · On-site +1

$112K - $153K/yr

Ensuring quality oversight and quality assurance and quality by design activities related to GCP/GCLP area * Guide and support from a quality perspective the GCP/GCLP and GPP related activities ...

Argenx

Clinical Quality Lead

$152K - $209K/yr

Provide QA input during the creation/revision of argenx clinical procedural documents for GCP compliance * When assigned as "QA Approver" in ARGO or PhoeniQS, act as QA approver for GCP area. * Act ...

Novartis

Associate Director, Clinical QA

East Hanover, NJ · On-site +1

$158K - $237K/yr

Provide GCP guidance to day-to-day questions arising from Clinical trials deliverables. * Collaborate with Country Development QA and ESP QA to drive initiatives relevant to internal monitoring and ...

ImmunityBio, Inc.

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 ...

ImmunityBio

Senior GCP Auditor

Culver City, CA · On-site +1

$88K - $108K/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 ...

next page

Showing results 1-20

All JobsRemote Gcp Qa Jobs

Remote Gcp Qa information

See salary details

$14

$31

$53

How much do remote gcp qa jobs pay per hour?

As of Jun 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 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 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 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.
More about Remote Gcp Qa jobs
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 job categories do people searching Remote Gcp Qa jobs look for? The top searched job categories for Remote Gcp Qa jobs are:
Remote Gcp Qa jobs near you
Infographic showing various Remote Gcp Qa job openings in the United States as of June 2026, with employment types broken down into 82% Full Time, 9% Part Time, and 9% Contract. Highlights an 100% Remote job distribution, with an average salary of $66,371 per year, or $31.9 per hour.
Associate Director, Quality Assurance GCP

Associate Director, Quality Assurance GCP

Crinetics Pharmaceuticals

Remote

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 13 days ago

Job description

Crinetics is a pharmaceutical company based in San Diego, California that develops much-needed therapies for people with rare endocrine diseases. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and robust pipeline across preclinical and clinical development. We are driven by science with a patient-centric and team-oriented culture. This is an exciting time to join Crinetics as we shape our organization into the world's premier fully integrated endocrine company from discovery to patients. Come join our team as we transform the lives of others.
Position Summary:
The Associate Director, Quality Assurance GCP supports the Good Clinical Practice (GCP) Quality Assurance (QA) function and performs day-to-day GCP QA operations. She/he will execute and/or ensure proper oversight of GCP QA activities, perform external and internal audits, support clinical phase 1 to phase 4 study team activities, review documents, support regulatory inspections, and enhance GCP QA infrastructure development. In alignment with updated ICH E6(R3) expectations, the Associate Director emphasizes flexible, proportionate, and risk-based quality oversight, maintains inspection readiness, and leads proactive, data-driven quality management via continuous identification and mitigation of quality risks.
Essential Job Functions and Responsibilities:
These may include but are not limited to:
  • Manage or perform clinical site, internal, TMF, GCP, and GLP vendor audits.
  • Generate and/or review GCP and GLP QA audit plans and schedules, tailoring scope and depth to study/process risk and complexity.
  • Generate and/or review and approve audit trend reports across programs to identify systemic issues and drive preventive actions.
  • Communicate, address, and prevent identified GCP compliance issues and trends.
  • Develop and manage audit programs.
  • Represent QA at program-wide (eg, Clinical Development Team or CRO) meetings and provide GCP guidance and feedback.
  • Serve as point of escalation for GCP compliance issues identified by clinical study teams or QA leads, and be responsible for informing the head of QA and Management.
  • Embed Quality-by-Design (QbD) and Critical-to-Quality (CtQ) principles into study planning and execution to prevent errors that matter.
  • Investigate, manage, and track GCP CAPAs, deviations, and other quality issues.
  • Collaborate with cross-functional teams to help ensure and strengthen data integrity, data governance, digital traceability, and participant protection.
  • Assist with serious breach assessments and notifications per regional requirements.
  • Provide guidance and support to Trial Master File activities.
  • Review study-specific documents.
  • Partner with cross-functional groups and promote compliance.
  • Attend governance meetings.
  • Identify and address quality systems gaps, including internal process improvements.
  • Author, review, or revise SOPs, Work Instructions, Policies, and/or Job Aids.
  • Deliver training to internal and external stakeholders.
  • Support regulatory inspections and inspection readiness activities.
  • Drive an inspection-readiness mindset (e.g., mock interviews, inspections, storyboards, document triage, front-room/back-room orchestration).
  • Prepare clinical sites for inspection readiness.
  • Review clinical study documents.
  • Support other Quality Assurance and Quality Systems activities.
  • Develop compliance strategies.
  • Provide input and expertise in vendor selection and oversight.
  • Prepare and/or assess key quality metrics to support continuous improvement and timely escalation of issues.
  • Draft and recommend Quality Agreements for GCP/GLP vendors.
  • Direct/supervise personnel; including coaching, mentoring, development, performance management, and administrative tasks.
  • Other duties as assigned.

Education and Experience:
Required:
  • Bachelor's degree in a science discipline and at least 10 years' experience in a QA function within the pharmaceutical/biotech industry (an equivalent combination of experience and education may be considered) with a minimum of 7 years' supervisory/leadership experience.
  • Minimum of 5 years of working in a QA GCP function.
  • Previous experience in inspection readiness and audits.
  • Previous experience in developing and implementing compliance activities.
  • Proven ability to cultivate and develop relationships with cross functional teams, vendors, sites, and other stakeholders.
  • Proven ability to interpret applicable FDA, EU and ICH guidelines related to GCP.
  • Strong working knowledge of GCP regulations.
  • Able to assess issues, perform thorough analysis on complex investigations, and resolve issues in a diplomatic and expeditious manner.

Preferred:
  • GVP and GLP knowledge, a plus.
  • Auditor certification and/or RQAP-GCP certification, a plus.
  • Strong interpersonal/collaboration, organization, and multi-tasking skills.

Physical Demands and Work Environment:
Physical Activities: On a continuous basis, sit at desk for a long period of time; intermittently answer telephone and write or use a keyboard to communicate through written means. Some walking and lifting up to 25 lbs. may be required. The noise level in the work environment is typically low to moderate. The physical demands described above are representative of those that must be met by an employee to successfully perform the essential functions and responsibilities of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions and responsibilities.
Travel:
You may be required to travel for up to 40% of your time.
The Anticipated Base Salary Range:
In addition to your base pay, our total rewards program consists of a discretionary annual target bonus, stock options, ESPP, and 401k match. We also provide top-notch health insurance plans for employees (and their families) to include medical, dental, vision and basic life insurance, 20 days of PTO, 10 paid holidays, and a winter company shutdown.
The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience and education. Crinetics Pharmaceuticals is a multi-state employer, and this salary range may not reflect positions that work in other states. Your recruiter can share more about the specific salary range during the hiring process.
Equal Opportunity Employer:
Crinetics is proud to be an Equal Opportunity Employer. We provide equal employment opportunities to all employees and employment applicants without regard to unlawful considerations of sex, sexual orientation, gender (including gender identity and/or expression), pregnancy, race, color, creed, national or ethnic origin, citizenship status, religion or similar philosophical beliefs, disability, marital and civil union status, age, genetic information, veteran status or any personal attribute or characteristic that is protected by applicable local, state or federal laws.
Salary Range
The salary range for this position is: $150000 - $186000.
In addition to your base pay, our total rewards program consists of a discretionary annual target bonus, stock options, ESPP, and 401k match. We also provide top-notch health insurance plans for employees (and their families) to include medical, dental, vision and basic life insurance, 20 days of PTO, 10 paid holidays, and a winter company shutdown.

Apply