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Temporary Qa Validation Jobs (NOW HIRING)

TTEC

Temp Quality Assurance Specialist

Austin, TX · Remote

$20 - $22/hr

As a Temporary Quality Assurance Specialist working remotely in the United States, youll be a part of bringing humanity to business. #experienceTTEC Our employees have spoken. Our purpose, team, and ...

Adecco

Quality Assurance

Durham, NC

$19.88/hr

... of temporary QA staff while ensuring compliance with company policies, ISO requirements, and safety procedures. Perks: • Pay starting at $19.88 per hour, plus overtime as needed. • Weekly ...

JPC Partners

QA Tester

JPC Partners is looking for an QA Tester - Build & Quality (Builder) with MarTech (Marketing ... The Tester will be responsible for configuring, building, and validating customer communications ...

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How much do temporary qa validation jobs pay per hour?

As of May 31, 2026, the average hourly pay for temporary qa validation in the United States is $52.00, according to ZipRecruiter salary data. Most workers in this role earn between $39.42 and $63.22 per hour, depending on experience, location, and employer.
What are the most commonly searched types of Qa Validation jobs? The most popular types of Qa Validation jobs are:
Temporary Qa Validation jobs near you

Quality Assurance Validation & IT, Director

CTI

Covington, KY • On-site, Remote

Full-time

Medical, PTO

Posted 13 days ago

Job description

What You'll Do: 

  • Lead and manage QA staff responsible for audit execution and IT quality initiatives.
  • Mentor QA team members and support development through training in best auditing practices and IT quality standards.
  • Drive IT Quality strategy through continuous improvement initiatives, special projects, and process enhancements.
  • Plan, conduct, and oversee IT and computerized systems audits, including internal, vendor, and for-cause to ensure compliance with GxP regulations, contractual obligations, and internal standards.
  • Prepare, or review, and approve audit plans, reports, and audit responses within defined timelines.
  • Support sponsor audits and regulatory authority inspections.
  • Report audit and inspection outcomes and support Root Cause Analysis (RCA), Corrective and Preventive Actions (CAPAs), and effectiveness checks through closure.
  • Monitor SaaS providers compliance using risk-based approaches and performance signals.
  • Partner cross-functionally (Vendor Management, IT, and Business teams) to ensure alignment on quality standards.
  • Support IT related vendor qualification and provide oversight of the GxP audit program.
  • Contribute audit insights and trends to Quality Risk Management for continuous risk mitigation.
  • Provide Quality oversight of Computer System Life Cycle (CSLC) activities, including implementation, validation, change management, maintenance, periodic review, and decommissioning.
  • Review and approve validation documentation and ensure adherence to data integrity and Electronic Records/Electronic Signatures (ERES) requirements.
  • Serve as QA Subject Matter Expert (SME) for CSLC frameworks and IT quality processes.
  • Ensure changes to systems and infrastructure are controlled, risk-assessed, and compliant with regulatory expectations.
  • Review IT related SOPs and policies.
  • Lead initiatives to strengthen data integrity, inspection readiness, and compliance processes.
  • Collaborate with IT and business functions to streamline GxP system compliance processes.
  • Support training programs to enhance organizational understanding of IT quality and compliance requirements.
  • Review and approve investigations, deviations, RCA, CAPAs, and effectiveness checks related to audits, inspections, and quality events. Ensure timely resolution and closure of quality events.

    What You'll Bring:

    • Bachelor's Degree or equivalent combination of education and experience
    • 5 years of experience in Software Development Life Cycle (SDLC), testing, and validation in a regulated industry and IT auditing (internal and vendors)
    • At least 10 years in CRO, pharmaceutical, clinical or related fields
    • Fluent in English

    About CTI

    CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of development, from drug concept to commercialization. CTI is headquartered in the Greater Cincinnati, OH region with global operations in collaboration with pharmaceutical, biotechnology, and medical device firms. For more information, visit www.ctifacts.com

    Why CTI?

    • Advance Your Career – We support career progression through a structured mentoring program and leadership courses that provide the support needed to grow. We also value ongoing education and training through tuition reimbursement and a dedicated training department.
    • Join an Award-Winning and Valued Team – We have an award-winning unparalleled culture that can be felt by our employees across 60 countries. We support a work-life balance and the importance of time with family by offering generous health benefits and vacation packages, hybrid work from home opportunities, and paid parental leave. We also encourage care for the world around us through our unique CTI Cares program.
    • Make a Lasting Impact – We focus on moving medicine forward by working on treatments for chronically and critically-ill patients, who depend on us to bring life-changing therapies to market.

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