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Internship Qc Data Reviewer Jobs (NOW HIRING)

Flourish Research

QC & Data Analyst

San Antonio, TX

We are actively hiring a QC & Data Analyst to support our San Antonio, TX site. LOCATION : Onsite ... Conduct a thorough and precise review of study charts utilizing SOPs, policies, GCP, GDP, and ...

Flourish Research

QC & Data Analyst

San Antonio, TX · On-site

We are actively hiring a QC & Data Analyst to support our San Antonio, TX site. LOCATION : Onsite ... Conduct a thorough and precise review of study charts utilizing SOPs, policies, GCP, GDP, and ...

Pace

GMP Data Reviewer (Pharma)

Oakdale, MN · On-site

$55K - $65K/yr

Gmp Data Reviewer Shift: Monday through Friday, 8:30 AM - 5:00 PM Are you ready to work making the ... or quality control data, standard operating procedures (SOPs), quality exceptions, logbooks ...

Pace

PLS GMP Data Reviewer (Pharma)

Oakdale, MN · On-site

$55K - $65K/yr

Gmp Data Reviewer Shift: Monday through Friday, 8:00 AM - 5:00 PM Are you ready to work making the ... or quality control data, standard operating procedures (SOPs), quality exceptions, logbooks ...

Integrated Resources INC

QC Reviewer

La Jolla, CA

We provide quality resources in four specialty areas: Information Technology (IT), Clinical ... Ability to review data across multiple documents for consistency. The candidate must be able to ...

Fladger Associates

QC Associate IV

Fremont, CA · On-site

Assists with QC's data management, including data review and trending. * Maintains specific QC files and database records for process and/or quality improvement efforts. * Maintain laboratory ...

Pacelabs

GMP Data Reviewer (Pharma)

Oakdale, MN · On-site

$55K - $65K/yr

... or quality control data, standard operating procedures (SOPs), quality exceptions, logbooks ... Analyzes and reviews intermediate to complex operations, results, feedback, and related quality ...

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How much do internship qc data reviewer jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for internship 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.
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Infographic showing various Internship Qc Data Reviewer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 11% Part Time, and 3% Contract. Highlights an 86% Physical, 3% Hybrid, and 11% Remote job distribution, with an average salary of $54,583 per year, or $26.2 per hour.

Quality Control Data Review Scientist - Nights

Cambrex

Charles City, IA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted yesterday

Cambrex rating

8.1

Company rating: 8.1 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

39th 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

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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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