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Qa Document Review Jobs (NOW HIRING)

Globe Telecom, Inc.

Bid Quality Assurance

Globe, AZ

Document Review and Approval * Conduct quality reviews of bid kits, supporting documents, and final ... Define and enforce QA standards, checklists, and review criteria for bid and accreditation ...

Collabera

Document Review Attorney

Carrollton, TX

... high quality IT resources through Staff Augmentation, Global Talent Management, Value Added ... DOCUMENT REVIEW ATTORNEY JOB IN CARROLLTON, TX (15 POSITIONS) PORTUGUESE and ENGLISH Title:

Collabera

Document Review Attorney

Carrollton, TX

... high quality IT resources through Staff Augmentation, Global Talent Management, Value Added ... Title: Document Review Attorney Location: Carrollton, TX Duration: 2 month (may extend) Manager ...

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All JobsQa Document Review Jobs

Qa Document Review information

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$15

$28

$43

How much do qa document review jobs pay per hour?

As of Jul 27, 2026, the average hourly pay for qa document review in the United States is $28.56, according to ZipRecruiter salary data. Most workers in this role earn between $22.12 and $32.93 per hour, depending on experience, location, and employer.

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

To excel as a QA Document Review Specialist, you need a solid understanding of quality assurance principles, attention to detail, and familiarity with regulatory requirements, often supported by a degree in life sciences or a related field. Experience with document management systems, quality management software, and knowledge of standards like ISO or GMP is typically required. Strong organizational skills, clear communication, and critical thinking help distinguish top performers in this role. These skills ensure accurate documentation, compliance with regulations, and the integrity of quality processes within the organization.

What is the difference between Qa Document Review vs Qa Analyst?

AspectQa Document ReviewQa Analyst
CredentialsTypically requires QA certifications, knowledge of documentation standardsRequires QA certifications, analytical skills, and understanding of quality processes
Work EnvironmentFocuses on reviewing and validating documents in regulated industriesInvolves analyzing quality data, performing audits, and process improvements
Industry UsageCommon in manufacturing, pharmaceuticals, and software developmentUsed across similar industries for quality assurance and process analysis

Qa Document Review primarily involves examining and validating quality documents to ensure compliance, while Qa Analyst focuses on analyzing quality data, performing audits, and improving processes. Both roles require QA certifications and are integral to maintaining quality standards in various industries.

What is a QA Document Review specialist?

A QA Document Review specialist is responsible for reviewing and ensuring the quality, accuracy, and compliance of documents within an organization, often in regulated industries like pharmaceuticals, healthcare, or manufacturing. Their duties typically include checking documents for completeness, adherence to company standards, and compliance with regulatory requirements. They may also assist in maintaining document control systems, training staff on document management procedures, and supporting audits. This role helps ensure that critical documentation is reliable, traceable, and meets both internal and external standards.

What are some common challenges faced by QA Document Review professionals, and how can they be managed effectively?

QA Document Review professionals often encounter challenges such as managing large volumes of documentation, ensuring strict compliance with regulatory requirements, and maintaining accuracy under tight deadlines. To address these, it's helpful to develop strong organizational skills, stay up-to-date with current industry regulations, and utilize document management software. Collaborating closely with cross-functional teams such as Quality Assurance, Regulatory Affairs, and Manufacturing can also facilitate efficient document review and ensure all standards are met.
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Qa Document Review jobs near you
Infographic showing various Qa Document Review job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 80% Full Time, 13% Part Time, 1% Temporary, and 5% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $59,398 per year, or $28.6 per hour.
Quality Assurance & Document Control Specialist

Quality Assurance & Document Control Specialist

3V Sigma USA

Georgetown, SC • On-site

Full-time

Posted 7 days ago

Job description

Job Type
Full-time
Description
Location: Georgetown, South Carolina
Work Arrangement: Full-time, on-site
3V Sigma is a global producer of specialty chemicals with approximately 500 employees and four manufacturing facilities in the United States and northern Italy. Our Georgetown facility brings together manufacturing, quality, engineering, R&D, and operations teams to produce innovative, high-quality products for customers around the world.
We are seeking a detail-oriented Quality Assurance & Document Control Specialist to support our quality systems and manufacturing operations. This position is responsible for maintaining controlled quality documents, reviewing production batch records, supporting quality investigations, and helping ensure compliance with ISO 9001:2015 and EFfCI requirements.
This is a good opportunity for someone who enjoys detailed work, understands the importance of accurate manufacturing records, and is comfortable working across multiple departments to keep quality processes moving.
What You'll Do
  • Maintain, organize, file, and archive-controlled quality documents and records.
  • Review completed batch sheets for accuracy, completeness, required approvals, and documented deviations.
  • Issue and release production batch sheets, box labels, and supersack labels.
  • Support Management of Change (MOC), Corrective and Preventive Action (CAPA), and Out-of-Specification (OOS) processes.
  • Assist with investigations involving batch-record deviations, product complaints, and other quality-related issues.
  • Maintain Technical Data Sheets (TDS), batch sheets, calibration lists, change request forms, procedures, and other controlled documents.
  • Write, revise, format, and route standard operating procedures, work instructions, forms, and quality documentation.
  • Track document revisions and help ensure current, approved versions are available to the appropriate departments.
  • Support internal audits and other quality activities related to ISO 9001:2015 and EFfCI requirements.
  • Work with Production, Quality Control, R&D, Engineering, and other departments to resolve documentation issues and improve processes.
  • Assist with employee training on quality procedures and documentation requirements after gaining the necessary experience.
  • Participate in corrective actions and continuous improvement initiatives.

Requirements
What We're Looking For
  • High school diploma or equivalent required.
  • Previous experience in quality assurance, document control, quality systems, or a regulated manufacturing environment is preferred.
  • An associate degree, technical training, or college coursework in quality, manufacturing, business, science, or a related field is helpful but not required.
  • Familiarity with ISO 9001:2015, document-control practices, CAPA, MOC, deviations, or batch-record review is strongly preferred.
  • Strong attention to detail and the ability to identify missing, inconsistent, or incomplete information.
  • Strong organizational skills with the ability to manage multiple documents, deadlines, and priorities.
  • Proficiency with Microsoft Word, Excel, Outlook, and PowerPoint.
  • Clear written and verbal communication skills.
  • Ability to work independently while also collaborating with employees across different departments.
  • Sound judgment when handling controlled or confidential information.
  • Experience writing or revising procedures and work instructions is a plus.
The Right Fit
The right candidate will be organized, dependable, and comfortable following established processes while also looking for practical ways to improve them. You should be willing to ask questions, follow up when documentation is incomplete, and work directly with manufacturing and technical teams to help maintain consistent quality standards.

Apply