This non-laboratory position is responsible for the detailed review and evaluation of analytical data generated from stability studies, method development activities, and laboratory investigations.
This non-laboratory position is responsible for the detailed review and evaluation of analytical data generated from stability studies, method development activities, and laboratory investigations.
This non-laboratory position is responsible for the detailed review and evaluation of analytical data generated from stability studies, method development activities, and laboratory investigations.
This non-laboratory position is responsible for the detailed review and evaluation of analytical data generated from stability studies, method development activities, and laboratory investigations.
Data Reviewer I (QC)
Albany, NY · On-site
This position will also support QA initiatives when necessary and collaborate with laboratory personnel to review data per cGMP compliance and data integrity. The Reviewer should incorporate sound ...
Data Reviewer I (QC)
Albany, NY · On-site
This position will also support QA initiatives when necessary and collaborate with laboratory personnel to review data per cGMP compliance and data integrity. The Reviewer should incorporate sound ...
This non-laboratory position is responsible for the detailed review and evaluation of analytical data generated from stability studies, method development activities, and laboratory investigations.
Quick apply
This non-laboratory position is responsible for the detailed review and evaluation of analytical data generated from stability studies, method development activities, and laboratory investigations.
This non-laboratory position is responsible for the detailed review and evaluation of analytical data generated from stability studies, method development activities, and laboratory investigations.
This non-laboratory position is responsible for the detailed review and evaluation of analytical data generated from stability studies, method development activities, and laboratory investigations.
GMP Data Reviewer (Pharma)
Oakdale, MN · On-site
$55K - $65K/yr
Data and records may be in the form of electronic or paper records or laboratory notebooks ... Analyzes and reviews intermediate to complex operations, results, feedback, and related quality ...
GMP Data Reviewer (Pharma)
Oakdale, MN · On-site
$55K - $65K/yr
Data and records may be in the form of electronic or paper records or laboratory notebooks ... Analyzes and reviews intermediate to complex operations, results, feedback, and related quality ...
Support QMS activities, including quality documentation, process monitoring, workflow reviews ... Support onsite laboratory data management, documentation, workflow coordination, and customer ...
Support QMS activities, including quality documentation, process monitoring, workflow reviews ... Support onsite laboratory data management, documentation, workflow coordination, and customer ...
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.
Key Responsibilities Laboratory & Clinical Data Review Responsibilities * Manage and coordinate training programs for laboratory and data review staff to ensure compliance with regulatory and ...
Key Responsibilities Laboratory & Clinical Data Review Responsibilities * Manage and coordinate training programs for laboratory and data review staff to ensure compliance with regulatory and ...
Key Responsibilities Laboratory & Clinical Data Review Responsibilities * Manage and coordinate training programs for laboratory and data review staff to ensure compliance with regulatory and ...
Key Responsibilities Laboratory & Clinical Data Review Responsibilities * Manage and coordinate training programs for laboratory and data review staff to ensure compliance with regulatory and ...
Key Responsibilities Laboratory & Clinical Data Review Responsibilities * Manage and coordinate training programs for laboratory and data review staff to ensure compliance with regulatory and ...
Quick apply
Key Responsibilities Laboratory & Clinical Data Review Responsibilities * Manage and coordinate training programs for laboratory and data review staff to ensure compliance with regulatory and ...
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.
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.
GCMS Data Review Analyst
$50K - $75K/yr
... Data Reviewer to join their analytical laboratory team. This position is ideal for an experienced analytical chemist who enjoys interpreting chromatographic data, ensuring data integrity, and ...
Quick apply
GCMS Data Review Analyst
$50K - $75K/yr
... Data Reviewer to join their analytical laboratory team. This position is ideal for an experienced analytical chemist who enjoys interpreting chromatographic data, ensuring data integrity, and ...
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.
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.
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 ...
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 ...
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 ...
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 ...
Data Reviewer, Quality Control
Tustin, CA · 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 ...
Data Reviewer, Quality Control
Tustin, CA · 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 ...
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.
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.
Associate Data Review Scientist
Lancaster, PA · On-site
$57K - $57K/yr
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a ... The Data Review requirement of this position will also allow for development and assignment of ...
Associate Data Review Scientist
Lancaster, PA · On-site
$57K - $57K/yr
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a ... The Data Review requirement of this position will also allow for development and assignment of ...
Associate Data Review Scientist
Lancaster, PA · On-site
$57K - $57K/yr
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a ... The Data Review requirement of this position will also allow for development and assignment of ...
Associate Data Review Scientist
Lancaster, PA · On-site
$57K - $57K/yr
In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a ... The Data Review requirement of this position will also allow for development and assignment of ...
Laboratory 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 laboratory data reviewer jobs pay per hour?
What is the difference between Laboratory Data Reviewer vs Laboratory Technician?
| Aspect | Laboratory Data Reviewer | Laboratory Technician |
|---|---|---|
| Credentials | Typically requires a bachelor's degree in a science field; certifications like ASCP may be preferred | Usually requires a high school diploma or associate degree; technical training often provided on the job |
| Work Environment | Office and laboratory settings, reviewing data and ensuring accuracy | Laboratory bench work, preparing samples, and conducting tests |
| Primary Responsibilities | Review and validate laboratory data, ensure compliance with protocols | Perform 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.

Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 19 days ago
Eurofins rating
7.4
Based on 180 frontline employees who took The Breakroom Quiz
57th of 105 rated laboratories
Job description
The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we focus on your professional growth by providing opportunities to build a rewarding career within the biopharmaceutical industry. Our supportive teams, comprehensive training, and commitment to work-life balance allow employees to develop their skills while contributing to meaningful scientific advancements.
Eurofins Scientific is an international life sciences company providing a unique range of analytical testing services to clients across multiple industries, helping make life and our environment safer, healthier, and more sustainable. From the food you eat to the medicines you rely on, Eurofins works with some of the world's largest companies to ensure product safety, authenticity, and quality.
Join us in shaping a safer, healthier, and more sustainable world. Explore opportunities with Eurofins and become part of a global team driving scientific excellence.
Eurofins PSS is seeking an Analytical Data Reviewer - LNP and Lipids to support analytical quality and compliance activities for lipid nanoparticle (LNP) formulations and lipid-based materials in a GMP-regulated environment.
This non-laboratory position is responsible for the detailed review and evaluation of analytical data generated from stability studies, method development activities, and laboratory investigations. The ideal candidate will possess strong analytical chemistry knowledge, experience reviewing chromatographic data, and a commitment to data integrity and regulatory compliance.
Responsibilities
- Review analytical data packages related to LNP formulations, lipid raw materials, stability studies, method development, and investigations.
- Evaluate chromatographic and analytical data generated from techniques such as HPLC, UPLC, and LC-MS for accuracy, completeness, and compliance.
- Verify calculations, data transcriptions, instrument outputs, and supporting documentation.
- Review OOS (Out-of-Specification) and OOT (Out-of-Trend) investigations for scientific soundness, completeness, and appropriate corrective actions.
- Ensure all records comply with GMP requirements, Good Documentation Practices, and applicable regulatory guidelines.
- Maintain review timelines and tracking systems to support sample release and regulatory submission milestones.
- Collaborate with Analytical Development, Quality Control, and Quality Assurance teams to address data discrepancies and resolve review findings.
- Support continuous improvement initiatives related to data review processes and compliance practices.
Minimum Qualifications
- Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline.
- 3-4 years of analytical laboratory experience within a GMP-regulated pharmaceutical, biotechnology, or biopharmaceutical environment.
- Experience generating and interpreting chromatographic data, including HPLC, UPLC, and/or LC-MS.
- Working knowledge of GMP regulations, data integrity principles, and Good Documentation Practices.
- Strong attention to detail and ability to identify inconsistencies within analytical datasets and documentation.
- Excellent organizational, time management, and multitasking skills.
- Ability to work both independently and collaboratively within cross-functional teams.
- Strong written and verbal communication skills.
Preferred Qualifications
- Experience reviewing analytical data within a QC, QA, or analytical development environment.
- Familiarity with lipid nanoparticle (LNP) technologies, lipid characterization, and related investigations.
- Experience supporting analytical method development or method lifecycle activities.
- Experience with electronic systems such as Veeva, SLIMS, JMP, LIMS, or similar laboratory software platforms.
- Authorization to work in the United States indefinitely without restriction or sponsorship.
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.
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