Analytical Sciences GMP Data Reviewer

Eurofins; New York; On-site; USD 36,000 - 41,000; Full time

Benefits offered by this job

Medical insurance

Dental & Vision coverage

401(k) with company match

Paid time off

Job summary

Eurofins USA PSS Insourcing Solutions is seeking an Analytical Chemistry Data Reviewer to review GMP laboratory data and documentation to ensure compliance with procedures, GDP standards, and regulatory requirements. A strong chemistry background and experience reviewing analytical data in a GMP environment are required.

The role involves GMP data review, documentation validation, and potential cross-training across laboratory testing functions.

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.

Responsibilities

• GMP Data & Documentation Review: verify data against procedures and GDP standards.
• Cross-Training & Laboratory Support: participate in cross-training and provide hands-on support when needed.
• Communication & Issue Resolution: resolve data annotations and discrepancies with teams.
• GDP & Good Documentation Practices: document activities following GDP expectations.
• Safety & Compliance: complete required trainings and maintain safety standards.

Skills

GMP data review

Documentation

Analytical testing

Communication

Education

BSc in Chemistry or Life Sciences

2+ years cGMP experience

Tools

HPLC/UPLC

UV-Vis spectrophotometry

ELISA

MCE

iCIEF

Job description

Company Description

At Eurofins PSS, we work with leading international companies across the pharma, medical device, food, cosmetic & consumer products industries - who all trust us with their mission-critical testing. For 20 years, our international network of teams have served clients at their sites, across 20 countries.

PSS® is part of Eurofins Scientific, an international life sciences company, providing a unique range of analytical testing services across multiple industries, through a network of over 950 laboratories in 60 countries, and c.a. 63,000 employees.

Job Description

The Analytical Chemistry Data Reviewer is responsible for reviewing GMP laboratory data and documentation to ensure compliance with established procedures, data integrity standards, and regulatory requirements. This role requires a strong chemistry background and experience reviewing analytical data in a GMP-regulated environment.

Key Responsibilities

GMP Data & Documentation Review

• 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

Cross-Training & Laboratory Support

• 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.

Communication & Issue Resolution

• Collaborate with testing personnel to resolve data annotations, discrepancies, or corrections
• Partner with laboratory teams to support compliance and continuous improvement initiatives

Good Documentation Practices (GDP)

• Accurately document activities in logbooks, notebooks, and electronic systems following GDP expectations

Safety & Compliance

• Conduct laboratory safety and compliance walkthroughs and document observations as required
• Complete all required safety, procedural, and refresher trainings on schedule

Qualifications

Education & Experience

• 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

Technical Skills

• Hands‑on experience with HPLC/UPLC and UV‑Vis spectrophotometry
• Experience with ELISA, MCE, and/or iCIEF preferred
• Proven ability to process and review quantitative liquid chromatography data

Physical Requirements

• Able to meet physical requirements, including lifting 25 lbs., prolonged standing or walking, pushing/pulling equipment, and bending or reaching for supplies

Additional Requirements

• 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

Additional Information

Position is Full Time, Monday-Friday, First Shift, Monday through Friday from 8am-4:30pm.

• Medical Coverage: Comprehensive medical insurance options
• Dental & Vision: Full dental and vision coverage available
• Life & Disability Insurance: Employer-sponsored plans
• Retirement: 401(k) plan with company match
• Paid Time Off: Vacation days, paid holidays, and additional PTO options
• Compensation: $26.25 - $30.00 per hour

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.