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Laboratory Data Reviewer Jobs (NOW HIRING)

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

Tustin, CA ยท On-site

$31.63 - $42.16/hr

Conduct GMP review of laboratory notebooks, logbooks, and associate forms. * Conduct GMP review of electronic raw data to ensure compliance with data integrity policies. * Support OOS/OOT ...

Laboratory Data Assistant

Burbank, CA ยท On-site

$22 - $25/hr

We are seeking a Laboratory Data Assistant for a temporary role to provide technical documentation ... Review technical documents for critical information and address any deficiencies with vendors

Laboratory Data Assistant

Burbank, CA ยท On-site

$22 - $25/hr

We are seeking a Laboratory Data Assistant for a temporary role to provide technical documentation ... Review technical documents for critical information and address any deficiencies with vendors

Data Reviewer, Quality Control

Tustin, CA ยท On-site

$31.63 - $42.16/hr

Conduct GMP review of laboratory notebooks, logbooks, and associate forms. * Conduct GMP review of electronic raw data to ensure compliance with data integrity policies. * Support OOS/OOT ...

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Laboratory Data Reviewer information

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How much do laboratory data reviewer jobs pay per hour?

As of Jun 29, 2026, the average hourly pay for laboratory 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 the difference between Laboratory Data Reviewer vs Laboratory Technician?

AspectLaboratory Data ReviewerLaboratory Technician
CredentialsTypically requires a bachelor's degree in a science field; certifications like ASCP may be preferredUsually requires a high school diploma or associate degree; technical training often provided on the job
Work EnvironmentOffice and laboratory settings, reviewing data and ensuring accuracyLaboratory bench work, preparing samples, and conducting tests
Primary ResponsibilitiesReview and validate laboratory data, ensure compliance with protocolsPerform laboratory tests, prepare samples, and operate lab equipment

The Laboratory Data Reviewer primarily focuses on reviewing and validating laboratory data to ensure accuracy and compliance, often working in an office setting. In contrast, the Laboratory Technician conducts hands-on laboratory work, preparing samples and performing tests. Both roles are essential in the lab environment but differ in responsibilities and required credentials.

More about Laboratory Data Reviewer jobs
What cities are hiring for Laboratory Data Reviewer jobs? Cities with the most Laboratory Data Reviewer job openings:
What states have the most Laboratory Data Reviewer jobs? States with the most job openings for Laboratory Data Reviewer jobs include:
Infographic showing various Laboratory Data Reviewer job openings in the United States as of June 2026, with employment types broken down into 18% Full Time, 68% Part Time, and 14% Nights. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $54,583 per year, or $26.2 per hour.

QC Data Reviewer - LNP and Lipids

Eurofins US Network

Boston, MA โ€ข On-site

Other

Medical, Dental, Vision, Life, Retirement, PTO

This job post hasย expired today.ย Applications are no longer accepted.


Job description

Boston, MA, USA

Full-time

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.

  • 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.

Qualifications

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.

  • 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).

  • Proficiency in GMP regulations and Good Documentation Practices.

  • 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.

Preferred Qualifications:

  • 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 Information

What to Expect in the Hiring Process:

  • 10-15 Minute Phone Interview with Region Recruiter

  • 45-60 Minute Virtual Interview with Manager and/or Group Leader

  • 30 Minute In-Person Onsite Meeting with the Team

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.