This non-laboratory role is responsible for reviewing and evaluating analytical quality data for LNP formulations and lipid materials across stability studies, method development, and investigations.
This non-laboratory role is responsible for reviewing and evaluating analytical quality data for LNP formulations and lipid materials across stability studies, method development, and investigations.
This non-laboratory role is responsible for reviewing and evaluating analytical quality data for LNP formulations and lipid materials across stability studies, method development, and investigations.
This non-laboratory role is responsible for reviewing and evaluating analytical quality data for LNP formulations and lipid materials across stability studies, method development, and investigations.
Data Reviewer, Quality Control Microbiology
Indianapolis, IN · On-site
$31.07 - $37.64/hr
Summary RayzeBio is seeking a Quality Control Microbiology Data Reviewer, reporting to the Director- Microbiology Quality Control The Data Reviewer will collaborate with the Radiation Safety Officer ...
Data Reviewer, Quality Control Microbiology
Indianapolis, IN · On-site
$31.07 - $37.64/hr
Summary RayzeBio is seeking a Quality Control Microbiology Data Reviewer, reporting to the Director- Microbiology Quality Control The Data Reviewer will collaborate with the Radiation Safety Officer ...
Data Reviewer, Quality Control Microbiology
Indianapolis, IN · On-site
$31.07 - $37.64/hr
Summary RayzeBio is seeking a Quality Control Microbiology Data Reviewer, reporting to the Director- Microbiology Quality Control. The Data Reviewer will collaborate with the Radiation Safety Officer ...
Data Reviewer, Quality Control Microbiology
Indianapolis, IN · On-site
$31.07 - $37.64/hr
Summary RayzeBio is seeking a Quality Control Microbiology Data Reviewer, reporting to the Director- Microbiology Quality Control. The Data Reviewer will collaborate with the Radiation Safety Officer ...
In addition to data review, this role will support QC data monitoring activities, including evaluation of release data, raw material testing data, and stability data trends to identify emerging ...
In addition to data review, this role will support QC data monitoring activities, including evaluation of release data, raw material testing data, and stability data trends to identify emerging ...
Data Reviewer, Quality Control Microbiology
Indianapolis, IN · On-site
$31.07 - $37.64/hr
Data Reviewer, Quality Control Microbiology
Data Reviewer, Quality Control Microbiology
Indianapolis, IN · On-site
$31.07 - $37.64/hr
Data Reviewer, Quality Control Microbiology
Assemble, review, and maintain Quality Control laboratory data to support accurate product disposition and timely material release. * Generate Certificates of Analysis (COAs) and other quality ...
Assemble, review, and maintain Quality Control laboratory data to support accurate product disposition and timely material release. * Generate Certificates of Analysis (COAs) and other quality ...
Quality Control Data Analyst
$96K - $134K/yr
Review, evaluate, and accurately label audio recordings and other data files using designated software tools and quality control procedures. * Inspect, classify, and analyze data according to ...
Quality Control Data Analyst
$96K - $134K/yr
Review, evaluate, and accurately label audio recordings and other data files using designated software tools and quality control procedures. * Inspect, classify, and analyze data according to ...
Assemble, review, and maintain Quality Control laboratory data to support accurate product disposition and timely material release. * Generate Certificates of Analysis (COAs) and other quality ...
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Assemble, review, and maintain Quality Control laboratory data to support accurate product disposition and timely material release. * Generate Certificates of Analysis (COAs) and other quality ...
Data Reviewer
Verona, WI · On-site
$35 - $43/hr
You will collaborate with QC chemists to address any data or reporting issues and escalate ... Review method validation data for accuracy, integrity, and regulatory compliance. * Work with ...
Data Reviewer
Verona, WI · On-site
$35 - $43/hr
You will collaborate with QC chemists to address any data or reporting issues and escalate ... Review method validation data for accuracy, integrity, and regulatory compliance. * Work with ...
Data Reviewer
Madison, WI · On-site
$35 - $43/hr
You will collaborate with QC chemists to address any data or reporting issues and escalate ... Review method validation data for accuracy, integrity, and regulatory compliance. * Work with ...
Data Reviewer
Madison, WI · On-site
$35 - $43/hr
You will collaborate with QC chemists to address any data or reporting issues and escalate ... Review method validation data for accuracy, integrity, and regulatory compliance. * Work with ...
The Quality Control Data Review Specialist is an effective member of the Laboratory Operations team. Position is accountable for driving results in a fast-paced environment by effectively performing ...
The Quality Control Data Review Specialist is an effective member of the Laboratory Operations team. Position is accountable for driving results in a fast-paced environment by effectively performing ...
Job Summary The Quality Control Data Review Specialist is an effective member of the Laboratory Operations team. Position is accountable for driving results in a fast-paced environment by effectively ...
Job Summary The Quality Control Data Review Specialist is an effective member of the Laboratory Operations team. Position is accountable for driving results in a fast-paced environment by effectively ...
Job Summary The Quality Control Data Review Specialist is an effective member of the Laboratory Operations team. Position is accountable for driving results in a fast-paced environment by effectively ...
Job Summary The Quality Control Data Review Specialist is an effective member of the Laboratory Operations team. Position is accountable for driving results in a fast-paced environment by effectively ...
The Quality Control Data Review Specialist is an effective member of the Laboratory Operations team. Position is accountable for driving results in a fast-paced environment by effectively performing ...
The Quality Control Data Review Specialist is an effective member of the Laboratory Operations team. Position is accountable for driving results in a fast-paced environment by effectively performing ...
Senior Data Reviewer, Quality Control
Verona, WI · On-site
$100K - $110K/yr
The Position The Senior Data Reviewer serves as a technical subject matter expert responsible for ... Provide oversight of external laboratory/CDMO data quality and compliance * Serve as a primary ...
Senior Data Reviewer, Quality Control
Verona, WI · On-site
$100K - $110K/yr
The Position The Senior Data Reviewer serves as a technical subject matter expert responsible for ... Provide oversight of external laboratory/CDMO data quality and compliance * Serve as a primary ...
Quality Control - Data Center Job Locations US-SC-Rock Hill Requisition ID 2026-12996 Category ... Review subcontractor quality plans for compliance to requirements * Inspect work conformance to ...
Quality Control - Data Center Job Locations US-SC-Rock Hill Requisition ID 2026-12996 Category ... Review subcontractor quality plans for compliance to requirements * Inspect work conformance to ...
(Senior) Manager, QC Documentation Compliance
Fremont, CA · On-site
$161K/yr
Manage the timely review of QC data processes to ensure data integrity and compliance with company SOPs and specifications, audit data packages for both scientific merit and GDP * Manage the data ...
(Senior) Manager, QC Documentation Compliance
Fremont, CA · On-site
$161K/yr
Manage the timely review of QC data processes to ensure data integrity and compliance with company SOPs and specifications, audit data packages for both scientific merit and GDP * Manage the data ...
Job Overview The Data Review Scientist will be responsible for reviewing laboratory data and ... Maintains and manages cGMP and controlled substance systems in all QC/PSG labs at defined levels of ...
Job Overview The Data Review Scientist will be responsible for reviewing laboratory data and ... Maintains and manages cGMP and controlled substance systems in all QC/PSG labs at defined levels of ...
Job Summary The Quality Control Data Review Specialist is an effective member of the Laboratory Operations team. Position is accountable for driving results in a fast-paced environment by effectively ...
Job Summary The Quality Control Data Review Specialist is an effective member of the Laboratory Operations team. Position is accountable for driving results in a fast-paced environment by effectively ...
Internship Qc Data Reviewer information
See salary details
$14.40 is the 25th percentile. Wages below this are outliers.
$12.98 - $15.73
48% of jobs
The median wage is $17.80 / hr.
$15.73 - $18.49
2% of jobs
$18.49 - $21.24
1% of jobs
$21.24 - $23.99
1% of jobs
$23.99 - $26.75
3% of jobs
$26.75 - $29.50
1% of jobs
$29.50 - $32.26
8% of jobs
$32.26 - $35.01
9% of jobs
$35.09 is the 75th percentile. Wages above this are outliers.
$35.01 - $37.76
9% of jobs
$37.76 - $40.52
6% of jobs
$40.52 - $43.27
9% of jobs
$12
$26
$43
How much do internship qc data reviewer jobs pay per hour?
As of Sep 4, 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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Eurofins rating
7.5
Based on 181 frontline employees who took The Breakroom Quiz
64th of 121 rated laboratories
Job description
Company Description
The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier, and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical, and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences, and in the support of clinical studies.
Join us in shaping a safer, healthier, and more sustainable world. Explore opportunities with Eurofins and be part of a global team driving scientific excellence. Apply today and make a meaningful impact!
Job Description
This non-laboratory role is responsible for reviewing and evaluating analytical quality data for LNP formulations and lipid materials across stability studies, method development, and investigations. The role requires attention to detail, familiarity with GMP practices, and the ability to ensure data integrity and regulatory compliance.
Minimum Required Qualifications:
Additional Details:
The position is Full Time, Monday-Friday, 8am-5pm. Candidates currently living within a commutable distance of Boston, MA are encouraged to apply.
Excellent full-time benefits include:
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.
The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier, and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical, and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences, and in the support of clinical studies.
Join us in shaping a safer, healthier, and more sustainable world. Explore opportunities with Eurofins and be part of a global team driving scientific excellence. Apply today and make a meaningful impact!
Job Description
This non-laboratory role is responsible for reviewing and evaluating analytical quality data for LNP formulations and lipid materials across stability studies, method development, and investigations. The role requires attention to detail, familiarity with GMP practices, and the ability to ensure data integrity and regulatory compliance.
- Review analytical data packages from stability studies, method development, and investigations for LNP and lipid-based products.
- Evaluate OOS/OOT investigation reports for completeness, scientific soundness, and appropriate corrective actions.
- Verify calculations, data transcriptions, and chromatographic data for accuracy and compliance.
- Ensure documentation adheres to GMP and applicable regulatory guidelines.
- Maintain review timelines and tracking logs to support release and regulatory submission deadlines.
- Partner with analytical and quality teams to resolve data discrepancies and review findings.
Minimum Required Qualifications:
- B.S. in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field with 3-4 years of analytical laboratory experience in a GMP-regulated pharmaceutical or biopharmaceutical environment.
- Proficiency in GMP regulations and Good Documentation Practices.
- Understanding of how chromatography is operated and how to interpret the data
- Strong organizational skills, attention to detail, and accuracy in documenting results.
- Strong time management and multitasking abilities.
- Ability to work independently and collaborate in a cross-functional environment.
- Effective communication and documentation skills.
- Experience with chromatograms and the ability to interpret chromatographic data such as HPLC, UPLC, and LC-MS (experience with chromatography data review is a plus).
- Familiarity with LNP and lipid technologies and investigations.
- Experience with method development.
- Experience with software systems such as SLIM, Veeva, JMP, and LIMS.
- Authorization to work in the United States indefinitely without restriction or sponsorship
Additional Details:
The position is Full Time, Monday-Friday, 8am-5pm. Candidates currently living within a commutable distance of Boston, MA are encouraged to apply.
Excellent full-time benefits include:
- Comprehensive medical coverage, dental, and vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holidays
- Annual rate is between $36.00-$40.00, depending on education and experience
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.
About Eurofins
Sourced by ZipRecruiter
Industry
Scientific research and development services, biotechnology research and development and environmental consulting services
Company size
10,000+ Employees
Headquarters location
Leacock, PA, US