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Qa Contractor Jobs (NOW HIRING)

QA Contractor, GMP Quality Assurance Location: Onsite at Research Triangle Park, NC Duration: 9 Months Travel: Domestic travel (less than 10% of the time) expected. Only W2 candidates are eligible ...

The QA Contractor's role in the project is to provide project monitoring, independent review, and technical support services to MN WIC during the e-WIC implementation phase of the project. The QA ...

As a QA Contractor, you will play a key role in ensuring product quality by executing and improving test processes, collaborating with engineering and QA leads, and supporting the delivery of high ...

QA Engineer-Remote

Omaha, NE ยท On-site

$40 - $45/hr

We have Contract role QA Engineer-Remote for client at Omaha NE. Please let me know if you or any ... As a contractor, you will immediately integrate into our active sprint cycles. You will be ...

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QA Contractor information

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$38K

$118.1K

$179K

How much do qa contractor jobs pay per year?

As of Aug 9, 2026, the average yearly pay for qa contractor in the United States is $118,074.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,000.00 and $144,500.00 per year, depending on experience, location, and employer.

What is the difference between Qa Contractor vs Qa Tester?

AspectQa ContractorQa Tester
CredentialsTypically requires QA certifications, experience in testing methodologiesOften requires similar certifications or experience in manual/automated testing
Work EnvironmentContract-based, project-specific, often freelance or temporary rolesFull-time or part-time employment within organizations or teams
Industry UsageCommon in tech, software development, and consulting firmsWidely used across software companies, IT departments, and product teams

Qa Contractors focus on short-term, project-based testing tasks, often working independently or with multiple clients. Qa Testers are typically employed full-time within organizations, performing ongoing testing activities. Both roles require similar skills and certifications, but differ mainly in employment type and work setup.

What is a QA contractor?

QA Contractors are quality assurance professionals hired on a contract basis to test software, products, or services for defects and ensure they meet specified standards. Unlike full-time employees, QA Contractors typically work for a set period or on specific projects. They may perform tasks such as manual testing, automated testing, writing test cases, and reporting bugs. Companies hire QA Contractors to supplement their teams during peak workloads or when specialized expertise is needed. Their work helps organizations deliver reliable and high-quality products to customers.

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

To thrive as a QA Contractor, you need a solid understanding of software testing methodologies, attention to detail, and experience with test case design, often supported by a degree in computer science or related certifications like ISTQB. Proficiency in testing tools such as Selenium, JIRA, and various automation frameworks is typically required. Strong analytical thinking, effective communication, and the ability to work independently are crucial soft skills in this role. These competencies ensure accurate defect detection, efficient collaboration with development teams, and the delivery of high-quality software products.

What are some common challenges QA contractors face when integrating with in-house development teams?

QA Contractors often need to quickly adapt to new team cultures, tools, and workflows, which can be challenging when joining established in-house development teams. Building effective communication channels and understanding project-specific testing requirements are crucial for success. It's also common to encounter varying expectations around documentation and reporting, so being proactive and clarifying deliverables early on helps ensure smooth collaboration. Staying up-to-date with the team's preferred testing frameworks and processes can significantly improve integration and productivity.
More about QA Contractor jobs
What cities are hiring for Qa Contractor jobs? Cities with the most Qa Contractor job openings:
What states have the most Qa Contractor jobs? States with the most job openings for Qa Contractor jobs include:
Infographic showing various Qa Contractor job openings in the United States as of August 2026, with employment types broken down into 71% Full Time, 9% Part Time, and 20% Contract. Highlights an 88% Physical, 1% Hybrid, and 11% Remote job distribution, with an average salary of $118,074 per year, or $56.8 per hour.

QA Contractor, GMP Quality Assurance

DivIHN

NC โ€ข On-site

Contractor

Re-posted 22 days ago


Job description

For further inquiries regarding the following opportunity, please contact our Talent Specialist, Hema at (630) 847-0275
Title:QA Contractor, GMP Quality Assurance
Location: Onsite at Research Triangle Park, NC
Duration: 9 Months
Travel: Domestic travel (less than 10% of the time) expected.
Only W2 candidates are eligible for this position. Third-party or C2C candidates will not be considered
Description:
The QA Contractor, GMP Quality Assurance, reporting to the Manager, GMP Quality Assurance, or designee, will be responsible for assisting in the management of client Quality Management System (QMS) and will strongly support client's Culture of Quality. This role will assure corporate compliance with applicable GMP national, international, and state regulations. This position will be based at our headquarters facility in RTP, NC.
Job Responsibilities
  • Manage assigned day-to-day QA responsibilities in support of the company's Quality Management Systems (QMS).
  • Provide timely support of Learning Management System, Change Control, Deviation Management Systems, or other QMS based customer requests.
  • Liaison with applicable department record owners to ensure their complete and timely resolution. Review and Approve said record types as assigned.
  • Provide accurate and timely weekly and quarterly QMS metric and Key Performance Indicator updates to QA and CMC senior management.
  • Collaborate successfully with the other departments to ensure that direct and supportive tasks are completed within project timelines.
  • Providing deliverables and resolving issues; Draft SOPs/controlled documents as well as perform quality unit review and approval of Quality Management Systems requests/ records related to Learning Management, Non-Conformance Management, CAPA management, and metric/KPI reporting.
  • Continually evaluate systems and procedures for improvement for efficiency and compliance to applicable regulatory requirements and standards.
  • Participate in project meetings as a Quality Unit representative and support colleagues by acting as a technical resource for quality and compliance related issues.
  • Perform daily customer-facing activities, as assigned by area management.
  • Maintain health of customer-facing activities such as document archival activities and notebook/logbook assignment and management.
  • Identify and collaborate with colleagues to implement continuous improvement initiatives; provide Quality Unit oversight of QMS based activities.
  • Assist in the qualification and oversight of vendors, contract manufacturers, contract laboratories, and service providers.
  • Support regulatory (FDA, EMA) and internal audits/inspections per client procedures and applicable regulatory requirements.
  • Communicate project status to stakeholders and escalate issues in a timely manner.
  • Perform and support other duties as assigned by area management.

About you
  • Bachelor's degree in a scientific field and 4+ years of experience in GMP based Quality Assurance, particularly in support/oversight of a company QMS, or 10+ years of GMP based Quality Assurance experience using a company QMS.
  • 3+ experience working within a pharmaceutical/biotech Quality Management system, such as Trackwise, ZenQMS, Veeva, is a requirement
  • Strong understanding of GMP guidelines and Quality Systems with the ability to apply GMPs in conformance to U.S. standards, and where appropriate, other regulatory authority standards.
  • Ability to author, review, and interpret Standard Operating Procedures (SOPs).
  • Ability to identify and/or resolve quality issues/discrepancies with others in a proactive, diplomatic, flexible, and constructive manner.
  • Strong attention to detail, highly organized and the ability to multitask in a fast-paced, highly interactive environment.
  • Strong service-oriented mindset with excellent verbal and written communication skills, and the ability to effectively collaborate with peers including scientific/technical colleagues.
  • Experience in analytical method validation and QC testing, especially in the fields of mammalian cell culture and Gene Therapy/Biologics based potency testing, is preferred.
  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).