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Full Time Qc Data Reviewer Jobs (NOW HIRING)

Sun Pharmaceutical Industries

Data Reviewer I

New Brunswick, NJ · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Perform thorough, in-depth reviews of Quality Control laboratory documentation and scientific data for completeness, accuracy, integrity, and compliance. * Review laboratory records including: * In ...

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 ...

Iff

Quality Control Data Specialist

Memphis, TN

Proficiency in Microsoft Office Suite, with advanced skills in Microsoft Excel for data analysis and reporting. * Communication and Collaboration: * Excellent communication skills, both written and ...

Woodhaven Furniture

Quality Control (Furniture)

Cairo, GA · On-site

$12.75/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Join the Woodhaven Furniture team in Cairo as a Full Time Quality Control professional and immerse yourself in a dynamic and customer-centric environment! As a key player in ensuring our handcrafted ...

Woodhaven Furniture

Quality Control (Furniture)

Cairo, GA · On-site

$12.75/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Join the Woodhaven Furniture team in Cairo as a Full Time Quality Control professional and immerse yourself in a dynamic and customer-centric environment! As a key player in ensuring our handcrafted ...

AMRI

Data Reviewer II

Albany, NY · On-site

$72K - $89K/yr

  • Retirement

Review quality control testing for compliance with internal SOPs and specifications * Assist in technical data review of the raw data generated for various compendial testing (such as USP/NF, EP, JP ...

Woodhaven Furniture

Quality Control (Furniture)

Cairo, GA · On-site

$12.75/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Join the Woodhaven Furniture team in Cairo as a Full Time Quality Control professional and immerse yourself in a dynamic and customer-centric environment! As a key player in ensuring our handcrafted ...

AMRI

Data Reviewer III

Albany, NY

$84K - $104K/yr

  • Retirement

The position will also support QA initiatives when necessary and collaborate with laboratory personnel to review data per cGMP compliance and data integrity. The Reviewer should incorporate sound ...

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All JobsQc Data Reviewer JobsFull Time Qc Data Reviewer Jobs

Full Time Qc Data Reviewer information

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$12

$26

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

As of Aug 15, 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?

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

Quality Control Data Review Scientist - Nights

Cambrex

Charles City, IA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 11 days ago

Cambrex rating

8.1

Company rating: 8.1 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

38th of 86 rated pharmaceutical

Job description

Company Information
You Matter to Cambrex.
Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance, drug product, and analytical services across the entire drug lifecycle. With more than 40 years of experience and a growing team of over 2,000 professionals servicing global clients, Cambrex is a trusted partner in branded and generic markets for API and dosage form development and manufacturing.
Your Work Matters.
At Cambrex, we strive to build a culture where all colleagues have the opportunity to:
  • engage in work that matters to our customers and the patients they serve
  • learn new skills and enjoy new experiences in an engaging and safe environment
  • strengthen connections with coworkers and the community

We're committed to attracting and nurturing a passionate team of valued professionals in our fast-paced and growing company. We offer a competitive benefits package that includes healthcare, life insurance, planning for retirement, and more!
Your Future Matters.
Known for our customer-focused scientific and manufacturing excellence, as well as our strong commitment to quality and safety, we offer a range of career and growth opportunities across our global network of locations. Together with our customers, we aim to improve the quality of life for patients around the world. Start a career where You Matter by applying today!
Job Overview
The Data Review Scientist will be responsible for reviewing laboratory data and supporting documentation to ensure that they are compliant with SOPs, and compendial and CGMP requirements. This individual must have knowledge of instrument theory in order to thoroughly vet and review data and draw conclusions based on collected data.
Responsibilities
Reviews raw technical data provided by technicians, chemists and laboratory supervision to ensure accuracy, completeness and correct scientific conclusions have been drawn. Data may include Analytical Records, notebooks, logbooks, spectra, chromatograms, other instrument output and any other information supporting Analytical Records.
  • Identifies data inaccuracies, incomplete inferences and works directly with laboratory staff to provide guidance and direction on the correction of laboratory data packages.
  • Verifies and ensures that conclusions drawn on laboratory data are sound and accurate and representative of materials under examination.
  • Maintains and manages cGMP and controlled substance systems in all QC/PSG labs at defined levels of compliance in accordance with site approved procedures and protocols.
  • Maintains open communication within and across departments to ensure timely delivery and approval of laboratory documents.
    Works alternative schedules to support output and data review of laboratories based on business need.

All employees are required to adhere to DEA, EPA, FDA and cGMP regulations as they relate to the operation of the Company; and to adhere to all company safety rules and procedures. All employees are expected to report to work regularly and promptly. Other duties relating to departmental mission, not specifically detailed in this section may be assigned.
Qualifications/Skills
  • Strong chemistry knowledge with proven ability to handle various project loads is beneficial.

Education, Experience & Licensing Requirements
Bachelor's degree in chemistry with three years' experience in a pharmaceutical and cGMP environment highly preferred.
  • Experience in a laboratory environment highly preferred.
  • Knowledge of analytical instrumentation (GC, HPLC, FTIR, UV-VIS, etc.) required.

Cambrex Charles City offers an extraordinary opportunity, a competitive salary, and an exceptional benefits package including medical, dental, vision care and prescription, life, LTD, STD; 401(k) with employer match; tuition reimbursement; and the 'Arthur I. Mendolia Scholarship Program.' Relocation assistance will be offered for this position.
Cambrex is an Equal Opportunity / Affirmative Action employer and will consider all qualified applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, protected veteran status, or disability status.
#LI-RD1
All requirements are subject to possible modifications to reasonably accommodate individuals with disabilities.

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About Cambrex

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

East Rutherford, NJ, US

Year founded

1981

Social media

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