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Eurofins PSS Insourcing SolutionsPosted 16 days ago

Analytical Sciences GMP Data Reviewer

Full-time
On-site
2+ years
Competitive
Posted 16 days ago

Eurofins PSS Insourcing Solutions is hiring an Analytical Sciences GMP Data Reviewer to review GMP laboratory data and documentation for compliance with procedures, data integrity standards, and regulatory requirements. The role also supports laboratory operations, documentation practices, safety, and issue resolution.

Posted
16 days ago
Source
linkedin.com
Sector
Healthcare

Opens the employer's application page in a new tab

Responsibilities

  • Review GMP data generated by laboratory personnel to ensure compliance with approved procedures
  • Verify logbook and documentation entries for accuracy, completeness, and adherence to GDP standards
  • Confirm the sample chain of custody throughout the testing lifecycle
  • Review audit trails to ensure actions align with procedural requirements and timelines
  • May be required to participate in cross-training opportunities across laboratory testing functions to broaden technical knowledge and enhance operational flexibility
  • Develop and maintain proficiency in applicable analytical testing techniques and laboratory processes as assigned
  • May be required to provide occasional hands-on laboratory testing support during periods of increased workload, staffing needs, or business priorities, when qualified and appropriately trained
  • Collaborate with laboratory personnel to ensure timely completion of testing activities while maintaining compliance with GMP, GDP, safety, and regulatory requirements
  • Collaborate with testing personnel to resolve data annotations, discrepancies, or corrections
  • Partner with laboratory teams to support compliance and continuous improvement initiatives
  • Accurately document activities in logbooks, notebooks, and electronic systems following GDP expectations
  • Conduct laboratory safety and compliance walkthroughs and document observations as required
  • Complete all required safety, procedural, and refresher trainings on schedule

Qualifications

  • Bachelor's degree in Chemistry, Life Sciences, or a related scientific field
  • 2+ years of cGMP experience in a regulated laboratory environment
  • Direct experience reviewing GMP data in an industrial setting
  • Hands-on experience with HPLC/UPLC and UV‑Vis spectrophotometry
  • Proven ability to process and review quantitative liquid chromatography data
  • Ability to learn new processes and manage multiple tasks simultaneously
  • Ability to follow instructions and comply with company policies and regulatory requirements
  • Authorized to work in the United States indefinitely without sponsorship

Preferred

  • Experience with ELISA, MCE, and/or iCIEF preferred

Required skills

CGMPELISAGMP Laboratory Data ReviewHPLCICIEFMCEUPLCUV-Vis Spectrophotometry

Full job description

Eurofins PSS Insourcing Solutions is hiring an Analytical Sciences GMP Data Reviewer to review GMP laboratory data and documentation for compliance with procedures, data integrity standards, and regulatory requirements. The role also supports laboratory operations, documentation practices, safety, and issue resolution.

Responsibilities

  • Review GMP data generated by laboratory personnel to ensure compliance with approved procedures
  • Verify logbook and documentation entries for accuracy, completeness, and adherence to GDP standards
  • Confirm the sample chain of custody throughout the testing lifecycle
  • Review audit trails to ensure actions align with procedural requirements and timelines
  • May be required to participate in cross-training opportunities across laboratory testing functions to broaden technical knowledge and enhance operational flexibility
  • Develop and maintain proficiency in applicable analytical testing techniques and laboratory processes as assigned
  • May be required to provide occasional hands-on laboratory testing support during periods of increased workload, staffing needs, or business priorities, when qualified and appropriately trained
  • Collaborate with laboratory personnel to ensure timely completion of testing activities while maintaining compliance with GMP, GDP, safety, and regulatory requirements
  • Collaborate with testing personnel to resolve data annotations, discrepancies, or corrections
  • Partner with laboratory teams to support compliance and continuous improvement initiatives
  • Accurately document activities in logbooks, notebooks, and electronic systems following GDP expectations
  • Conduct laboratory safety and compliance walkthroughs and document observations as required
  • Complete all required safety, procedural, and refresher trainings on schedule

Preferred

  • Experience with ELISA, MCE, and/or iCIEF preferred
  • ELISA
  • MCE
  • iCIEF

Benefits

  • Comprehensive medical insurance options
  • Full dental and vision coverage available
  • Employer-sponsored life and disability insurance plans
  • 401(k) plan with company match
  • Vacation days, paid holidays, and additional PTO options

Company

  • Managed scientific insourcing services for client sites
  • Luxembourg, Luxembourg, LUX
  • https://www.eurofinspss.com/
  • Founded in 2020
  • 1001-5000 employees

Qualifications

  • Bachelor's degree in Chemistry, Life Sciences, or a related scientific field
  • 2+ years of cGMP experience in a regulated laboratory environment
  • Direct experience reviewing GMP data in an industrial setting
  • Hands-on experience with HPLC/UPLC and UV‑Vis spectrophotometry
  • Proven ability to process and review quantitative liquid chromatography data
  • Ability to learn new processes and manage multiple tasks simultaneously
  • Ability to follow instructions and comply with company policies and regulatory requirements
  • Authorized to work in the United States indefinitely without sponsorship
  • Experience with ELISA, MCE, and/or iCIEF preferred

Required skills

  • CGMP, ELISA, GMP Laboratory Data Review, HPLC, ICIEF, MCE, Quantitative Liquid Chromatography Data Review, UPLC, UV-Vis Spectrophotometry

Preferred skills

  • Experience with ELISA, MCE, and/or iCIEF preferred

Experience

  • 2+ years

Job details

Employment type

Full-time

Seniority level

2+ years

Date posted

Oct 28, 2026

Work mode

On-site

Job source

linkedin.com

Company

Eurofins PSS Insourcing Solutions

Healthcare

Managed scientific insourcing services for client sites

  • Rensselaer County, NY
  • Healthcare
  • 1001-5000 employees
  • Founded 2020
  • eurofinspss.com

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