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Full Time Qc Data Reviewer Jobs (NOW HIRING)

CEDENT

Data Reviewer, Quality Control

Verona, WI

The Data Reviewer is responsible for ensuring the completion, quality, and compliance of laboratory data and reports produced within the Quality Control (QC) team. This includes the technical review ...

Avid Bioservices

Data Reviewer, Quality Control

Tustin, CA · On-site

$31.63 - $42.16/hr

The Data Reviewer, Quality Control 's main responsibility will be to review Quality Control ... This role is a full-time position. Days and hours of work are Monday through Friday, 8:00 a.m. to 5 ...

AMRI

Data Reviewer III

Rensselaer, NY

Quality Control Data Reviewer III - Onsite position in Rensselaer, NY Build your future at Curia, where our work has the power to save lives Curia is a global contract development and manufacturing ...

Santa Fe County

Quality Control Data Analyst

Santa Fe, NM · On-site

$53K - $61K/yr

Primary Purpose Under the direct supervision of the Quality Control Manager, analyzes and audits data and information that is being entered and/or changed in the Assessor's Office databases to ensure ...

Santa Fe County

Quality Control Data Analyst

Santa Fe, NM · On-site

$53K - $61K/yr

Santa Fe, NM Job Type: Full-Time Job Number: 202600186 Department: Assessor's Office Opening Date ... Quality Control Manager, analyzes and audits data and information that is being entered and/or ...

Seismic Works

Data QC - Data Processor

Houston, TX

As Data QC/Data Processor you will be responsible in inspecting the quality of raw data by analyzing observer logs compiled by data acquisition crews using a series of employer's propriety software ...

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Full Time Qc Data Reviewer information

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How much do full time qc data reviewer jobs pay per hour?

As of Jun 10, 2026, the average hourly pay for full time qc data reviewer in the United States is $26.24, according to ZipRecruiter salary data. Most workers in this role earn between $14.42 and $36.30 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Full Time QC Data Reviewer, and why are they important?

To thrive as a Full Time QC Data Reviewer, a strong background in data analysis, attention to detail, and familiarity with quality control standards—often supported by a degree in life sciences or a related field—is essential. Proficiency with laboratory information management systems (LIMS), data review software, and knowledge of regulatory guidelines like GMP or GLP is typically required. Excellent organizational skills, critical thinking, and effective communication help ensure accuracy and timely reporting. These skills and qualities are crucial for maintaining data integrity, regulatory compliance, and the overall reliability of scientific or manufacturing processes.

What are some common challenges faced by Full Time QC Data Reviewers, and how can these be managed effectively?

Full Time QC Data Reviewers often encounter challenges such as tight deadlines, managing large volumes of data, and ensuring strict compliance with regulatory standards. These challenges can be managed by maintaining strong organizational skills, staying updated on quality guidelines, and leveraging digital tools to streamline the review process. Additionally, effective communication with laboratory analysts and other quality teams is essential to quickly resolve discrepancies and maintain data integrity.

What does a Full Time QC Data Reviewer do?

A Full Time QC (Quality Control) Data Reviewer is responsible for reviewing and verifying data generated during laboratory testing or production processes to ensure accuracy, completeness, and compliance with regulatory standards. They check documentation, identify errors or inconsistencies, and work with laboratory staff to resolve issues before final data approval. The role is crucial in industries such as pharmaceuticals, biotechnology, and food manufacturing, where data integrity and regulatory compliance are critical. QC Data Reviewers help maintain high-quality standards and support audits or inspections by ensuring all records are accurate and up to date.

What is the difference between Full Time Qc Data Reviewer vs Clinical Data Coordinator?

AspectFull Time Qc Data ReviewerClinical Data Coordinator
CredentialsTypically requires a degree in life sciences or related field, often with certifications like CDMP or CDISCRequires a degree in health sciences, nursing, or related fields; certifications may include CDISC or clinical research certifications
Work EnvironmentWorks in clinical trial settings, reviewing data quality and consistencyCoordinates data collection, entry, and management in clinical research projects
Employer & IndustryPharmaceutical companies, CROs, biotech firmsResearch institutions, hospitals, pharmaceutical companies

While both roles involve clinical data, the Full Time Qc Data Reviewer primarily focuses on reviewing and ensuring data quality, whereas the Clinical Data Coordinator manages data collection and entry processes. The reviewer ensures data accuracy, while the coordinator oversees data flow and compliance throughout the trial.

What cities are hiring for Full Time Qc Data Reviewer jobs? Cities with the most Full Time Qc Data Reviewer job openings:
What are the most commonly searched types of Qc Data Reviewer jobs? The most popular types of Qc Data Reviewer jobs are:
Full Time Qc Data Reviewer jobs near you
Data Reviewer, Quality Control

Data Reviewer, Quality Control

CEDENT

Verona, WI

Full-time

Posted 19 days ago

Job description

The Data Reviewer is responsible for ensuring the completion, quality, and compliance of laboratory data and reports produced within the Quality Control (QC) team. This includes the technical review of analytical testing data and related notebooks, forms, logbooks, and more as specified by Standard Operating Procedures (SOPs). This position will evaluate data to ensure compliance with analytical methods, specifications, Good Laboratory Practices (GLP) or Good Manufacturing Practices (GMP) standards. This position will manage deadlines for review completion and aid in the organization and maintenance of data. The ideal candidate will have experience with analytical testing, either in performance or technical review.
Responsibilities
  • Evaluate QC laboratory data for compliance with analytical methods, protocols, specifications, and SOPs.
  • Review sample analysis results for completeness and accurate representation of the data and report findings.
  • Communicate with QC laboratory staff to proactively address the quality of laboratory documentation.
  • Prepare statements noting deficiencies with the analytical data set or notebooks and reports deficiencies to the project leader for correction.
  • Conduct SOP review and writing as well as conducts consultations for quality records.
  • Work cross-functionally to harmonize data review practices and produce a consistent product.
  • Perform other duties as assigned.
Requirements:
  • Bachelor’s degree in Chemistry (or related scientific field) with 2+ years’ relevant experience (pharmaceutical CMO/CRO).
  • Knowledge of cGMP and cGLP guidelines for contract manufacturing and analytical laboratories and ICH/FDA guidance documents.
  • Strong verbal and written communication skills and ability to work with diverse professionals in a matrix environment.
  • Solid organizational skills with ability to adapt to changing priorities and deadlines.
Preferred:
  • Language Skills: Ability to read, analyze and interpret SOPs, test methods, procedural guides and associated technical documents. Ability to write in a clear and concise manner. Ability to effectively present information and respond to questions from management, peers and colleagues.
  • Mathematical Skills: Ability to perform complex math functions, compute ratios, rate, and percent. Ability to draw and interpret graphs and charts.
  • Reasoning Skills: Ability to solve practical problems and interpret a variety of instructions furnished in written, oral, diagram or schedule form.
  • Other Skills and Abilities: Ability to work with people at various levels of the organization. Basic knowledge of computers and PC’s. Ability to use windows-based software including MS Office and chromatography data collection software. Basic knowledge of laboratory equipment, procedures, and analytical testing.
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About Cedent

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CEDENT strives to attract and retain the best people and provide an environment where they can all develop professionally and build a rewarding career. As a result, we create an inclusive environment that is rich in diversity, acknowledges each individual's uniqueness and promotes respect, personal achievement and stewardship. Our clients are global and so is CEDENT. We build and maintain a global workforce that includes people from different backgrounds, with a vast range of skills and experience all united by a common culture and commitment to help our clients achieve high performance. Cultivating a diverse workforce and inclusive work environment makes business sense. Our peoples varied skills are the talent engine that powers CEDENT, enabling it in turn to deliver the innovative solutions that help our clients outperform competitors.

Industry

It services

Company size

11 - 50 Employees

Headquarters location

Plano, TX, US

Year founded

2008

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