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Quality Control Document Reviewer Jobs (NOW HIRING)

As part of the Milford site's Quality Control team, the Data Reviewer is responsible for the cGMP analytical data review and documentation generated during laboratory analysis in the quality control ...

Quality Control Manager

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$115K - $160K/yr

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Quality Control (QC) Manager Apache Fabricators LLC Location: Houston, TX / Shop Environment ... quality documentation. * Review customer specifications, ITPs (Inspection Test Plans), WPS/PQRs ...

The Document Reviewer Specialist is responsible for the timely review, verification, reconciliation, control, and administration of production, processing, quality, and regulatory documentation ...

Document Quality Control Clerk

Radford, VA · On-site

$30.58 - $53.51/hr

Parsons is looking for an amazingly talented Document Quality Control Clerk to join our team! What ... Expedites review, signature approval, and release of supplier and internally produced documents.

Quality Control Inspector, La Vergne TN Pay Range: 21.47 Overview We are looking for skilled ... Drawing review * Documentation entry * Scrap reporting * Inventory check * Department support

Quality Control Scientist

Vista, CA · On-site

$30.01 - $41.27/hr

Performing analytical analysis and reviewing data for completeness and accuracy * Maintain a cGMP quality level of work for the QC operations to include training, documentation and procedural work

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Quality Control Document Reviewer information

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$158K

How much do quality control document reviewer jobs pay per year?

As of Sep 9, 2026, the average yearly pay for quality control document reviewer in the United States is $98,940.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,000.00 and $118,000.00 per year, depending on experience, location, and employer.

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Clinical Quality Control Reviewer

Collegeville, PA • On-site

Integrated Resources
Recruiting and Staffing Services • 51 - 200 employees

Other

Re-posted 26 days ago


Job description

Clinical Quality Control Reviewer

A Few Words About Us - Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description

Responsibilities:

  • Independently performs data quality review/quality control on clinical components of assigned documents (eg, clinical study reports, investigator brochures, manuscripts, summary documents, regulatory responses, etc.).
  • Formally documents findings of assigned documents.
  • Supports accuracy, internal consistency, uniformity and compliance with clinical and regulatory commitments and expectations.
  • Alerts supervisor and document authors immediately if significant problems are found during a review.
  • After completion or throughout the review, prepares written report of findings and record of the DQR/QC.
  • Participates in resolution of findings with the document authors, clinicians and other members of the medicine team if necessary.
  • Archives relevant documentation in the appropriate repository according to established departmental practices.
  • Manages the completion of complex tasks by applying technical skills and specialized knowledge to coordinate initial findings, conduct root cause analyses and corrective action planning with customers as necessary.

Reporting Tasks:

  • Provides ongoing analysis of data resulting from the quality review of regulatory submission documents.
  • Records assignments in relevant tasks logs.

Experience:

  • Minimum 3 years of clinical and data management experience in the pharmaceutical/healthcare industry.
  • This should also include a minimum of 3 years medical writing and DQR/QC experience of clinical documents.
  • An understanding of scientific principles, knowledge of medical terminology and familiarity with the AMA Manual is required.
  • The ability to edit to clear writing is required, as are strong verbal, written, and interpersonal communication skills, and the ability to pay rigorous attention to detail while working rapidly and accurately. Preparation of clinical regulatory documents is strongly preferred.
  • This experience can be obtained in a clinical setting, at a pharmaceutical company or CRO.
  • No Travel/No Overtime
Qualifications

Education:

  • At a minimum, a scientific or technical degree.
  • In general candidates would have a BS degree or equivalent.

Kind Regards

Sukhpreet Basra

Clinical Recruiter

Integrated Resources, Inc.

IT Life Sciences Allied Healthcare CRO

Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I

Direct:732-429-1921 (Tel) 732-549-2030*241 | (F) 732-549-5549

Gold Seal JCAHO Certified ™ for Health Care Staffing

"INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES" (8th Year in a Row)


Integrated Resources logo

About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996