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Data Review Chemist Jobs (NOW HIRING)

Optiq Health Labs

Analytical Chemist

Santa Ana, CA · On-site

Review chromatographic data and identify integration, calibration, or quality issues. * Document ... Bachelor's degree in chemistry, biochemistry, biology, chemical engineering, or a related field.

ARL

Data Processing Chemist

Oklahoma City, OK · On-site

$23 - $26/hr

Maintain data review and compliance with adherence to department standard operation procedures ... Associate Degree in Chemistry or related Science Field- or equivalent Diploma with 1 year of ...

COLEMAN CONSULTING GROUP LLC

Chemist 1

Athens, GA · On-site

As a Chemist, you will be working as part of a larger team conducting daily, routine testing of ... data review or conducting laboratory support activities with direction and oversight as well as ...

COLEMAN CONSULTING GROUP LLC

Chemist 4

Athens, GA · On-site

... data review, or conducting laboratory support activities as well as a sufficiently broad knowledge and versatility to lead SOP/method development and support additional assigned tasks as needed.

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How much do data review chemist jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for data review chemist in the United States is $30.99, according to ZipRecruiter salary data. Most workers in this role earn between $24.04 and $35.58 per hour, depending on experience, location, and employer.

What is a data review chemist?

Data Review Chemists are professionals responsible for reviewing and validating scientific data generated in laboratories, particularly in industries like pharmaceuticals, environmental testing, and food safety. They ensure the accuracy, integrity, and compliance of laboratory data with regulatory standards such as Good Laboratory Practice (GLP) or Good Manufacturing Practice (GMP). Their role involves checking raw data, calculations, and final reports, as well as identifying discrepancies or errors that could affect data quality. Data Review Chemists play a critical part in maintaining data reliability and supporting the release of safe and effective products to the market.

What are the key skills and qualifications needed to thrive as a data review chemist?

To thrive as a Data Review Chemist, you need a solid background in chemistry, analytical techniques, and experience with laboratory data review, often supported by a degree in chemistry or a related field. Familiarity with laboratory information management systems (LIMS), chromatography data systems (CDS), and Good Laboratory Practice (GLP) guidelines is typically required. Attention to detail, critical thinking, and strong written communication are essential soft skills for accurately interpreting and documenting complex data. These skills and qualifications ensure data integrity, regulatory compliance, and reliable results in scientific research and quality assurance environments.

What are some common challenges faced by data review chemists when ensuring data integrity, and how can they be addressed?

Data Review Chemists often encounter challenges such as incomplete documentation, inconsistent data entries, and discrepancies between raw data and reported results. Addressing these issues involves thorough attention to detail, effective communication with laboratory analysts, and strong knowledge of regulatory guidelines such as Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). Utilizing standardized review checklists and keeping up-to-date with training can also help ensure data integrity and compliance. Collaboration with QA teams and regular audits further support a robust review process.
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Data Review Chemist jobs near you
Infographic showing various Data Review Chemist job openings in the United States as of August 2026, with employment types broken down into 73% Full Time, 18% Contract, and 9% Nights. Highlights an 100% In-person job distribution, with an average salary of $64,466 per year, or $31 per hour.

Quality Control Data Review Scientist - Nights

Cambrex

Charles City, IA

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 16 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!

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, and Licensing Requirements: (Text Only)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-RD1Employment Type: FULL_TIME

What Cambrex employees say

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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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