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Per Diem 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 ...

ICON

Medical Data Reviewer

May be involved in review and QC clinical data sections for abstracts / manuscripts/ oral and poster presentations * Will collaborate closely with Regeneron Clinical Scientists, Medical Directors ...

Ultimate LLC

QC Data Entry Clerk

Irvine, CA · On-site

$20 - $21/hr

We are hiring for a contract Quality Control Data Entry Clerk Hourly Pay rate $20.00 - $21.00 per ... Review QC priority list. * Review IQC report for the sample lot batch size and exact P.O. number of ...

New

Curia, Inc.

Data Reviewer II

Albany, NY · On-site

$72K - $89K/yr

  • Retirement

... data per cGMP compliance and data integrity. The Reviewer should incorporate sound judgement ... Responsibilities * Review quality control testing for compliance with internal SOPs and ...

curiate.co

Data Reviewer II

Albany, NY · On-site

$72K - $89K/yr

  • Retirement

... data per cGMP compliance and data integrity. The Reviewer should incorporate sound judgement ... Responsibilities * Review quality control testing for compliance with internal SOPs and ...

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 ...

Skilled Up Solutions

Quality Control

Louisville, KY

$25 - $30/hr

Analyze quality control data to identify trends and areas for improvement. * Collaborate with production teams to set up welding processes and ensure optimal quality control measures are in place.

RMS Energy

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

We're looking for a Technical Data Reviewer who's excited to support data accuracy, organization ... Compensated Travel Time plus Per Diem - Earn while seeing new places * Education Support - Paid ...

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 ...

Thermo Fisher

Data Reviewer, Biopharma - Remote

Data Reviewer- Remote, Biopharma At PPD, part of Thermo Fisher Scientific, you'll discover ... Prepares QC statements noting deficiencies with the analytical data set or notebooks. * Reports ...

New

Pace

GMP Data Reviewer (Pharma)

Oakdale, MN · On-site

$55K - $65K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Compensation: $55,000 - $65,000 per year The salary for this position reflects a variety of factors ... or quality control data, standard operating procedures (SOPs), quality exceptions, logbooks ...

Pacelabs

GMP Data Reviewer (Pharma)

Oakdale, MN

$55K - $65K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Compensation: $55,000 - $65,000 per year The salary for this position reflects a variety of factors ... or quality control data, standard operating procedures (SOPs), quality exceptions, logbooks ...

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Per Diem Qc Data Reviewer information

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

As of Aug 16, 2026, the average hourly pay for per diem 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 is a per diem QC data reviewer?

A Per Diem QC (Quality Control) Data Reviewer is a professional who works on a flexible, as-needed basis to review and verify data in quality control processes, often within pharmaceutical, biotechnology, or laboratory environments. Their main responsibility is to ensure the accuracy, completeness, and compliance of laboratory data with regulatory standards and company procedures. They may review test results, documentation, and reports to identify discrepancies or errors that could impact product quality or regulatory compliance. Per diem positions offer flexibility and are often used to support high workloads or special projects. These roles are critical in maintaining data integrity and ensuring that products meet required quality standards.

What is the difference between Per Diem Qc Data Reviewer vs Per Diem Data Coordinator?

AspectPer Diem Qc Data ReviewerPer Diem Data Coordinator
CredentialsTypically requires a degree in life sciences or related field, with experience in data reviewOften requires similar educational background, with focus on data management skills
Work EnvironmentWorks in clinical trial settings, reviewing data for accuracy and complianceManages data entry, organization, and coordination across trial sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsResearch organizations, clinical trial sponsors, CROs

The Per Diem Qc Data Reviewer primarily focuses on reviewing clinical data for quality and accuracy, while the Per Diem Data Coordinator handles data management and coordination tasks. Both roles require similar educational backgrounds and work within the clinical research industry, but their daily responsibilities differ significantly.

What are the key skills and qualifications needed to thrive as a per diem QC data reviewer?

To thrive as a Per Diem QC Data Reviewer, you need strong analytical abilities, attention to detail, and a background in life sciences or a related field, often supported by a bachelor's degree. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practice (GMP) regulations, and relevant data review software is typically required. Excellent organizational skills, effective communication, and the ability to work independently are valuable soft skills for this role. These competencies ensure accurate data review, regulatory compliance, and reliable quality control in pharmaceutical or biotechnology environments.

What are some common challenges faced by per diem QC data reviewers and how can they be addressed?

Per Diem QC Data Reviewers often face challenges such as managing fluctuating work volumes, adapting to varying protocols across projects, and maintaining accuracy under tight deadlines. Since the role is typically flexible or on-call, time management and the ability to quickly familiarize oneself with new datasets or procedures are essential. To address these challenges, it helps to develop strong organizational skills, maintain up-to-date knowledge of quality standards, and communicate proactively with project managers and laboratory teams to clarify expectations and resolve discrepancies efficiently.
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Per Diem Qc Data Reviewer jobs near you
Infographic showing various Per Diem Qc Data Reviewer job openings in the United States as of August 2026, with employment types broken down into 78% Full Time, and 22% Contract. Highlights an 100% In-person job distribution, with an average salary of $54,583 per year, or $26.2 per hour.

Quality Control Data Review Scientist - Days

Cambrex

Charles City, IA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 23 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.

What Cambrex employees say

Pay

Benefits

Hours and flexibility

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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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