GMP Analytical Chemistry Data Reviewer

LabRulez; City of Rensselaer (NY); Hybrid; USD 36,000 - 41,000; Full time

Benefits offered by this job

Medical Coverage

Dental & Vision

401(k) Plan

Paid Time Off

Job summary

Eurofins Scientific is an international life sciences company dedicated to safety, authenticity, and quality across food, water, medicines, and cosmetics testing. The GMP Analytical Chemistry Data Reviewer role supports reviewing laboratory data to ensure regulatory compliance, data integrity, and proper documentation in a GMP environment.

The position emphasizes cross-training across testing functions, collaboration with lab personnel, and maintaining safety and GDP standards within a full-time

Qualifications

• Bachelor’s degree in Chemistry, Life Sciences, or related field.
• 2+ years of cGMP experience in a regulated lab.
• Direct experience reviewing GMP data in an industrial setting.

Responsibilities

• Review GMP data and documentation for compliance with procedures and GDP standards.
• Verify logbook entries for accuracy and adherence to GDP.
• Ensure sample chain of custody throughout testing lifecycle.
• Review audit trails to confirm procedural compliance and timelines.
• Cross-train across lab functions to broaden technical knowledge.
• Provide hands-on testing support when needed and trained.
• Collaborate with lab teams to meet testing deadlines while maintaining GMP/GDP compliance.

Skills

HPLC/UPLC

UV-Vis spectrophotometry

ELISA

MCE

iCIEF

Education

Bachelor's degree in Chemistry or Life Sciences

Job description

Analytical chemist, Administrative Assistant, Molecular biology

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.

In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

In 2025, Eurofins generated total revenues of EUR 7.296 billion, and has been among the best performing stocks in Europe over the past 20 years.

GMP Analytical Chemistry Data Reviewer

Job Description

TheAnalytical Chemistry Data Revieweris 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.


• 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 withHPLC/UPLCandUV‑Vis spectrophotometry


• Experience withELISA, MCE, and/or iCIEFpreferred


• 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 isFull Time, Monday-Friday, First Shift, Monday through Friday from 8am-4:30pm.Candidates currently living within a commutable distance ofRensselear, New York,are encouraged to apply

Excellent full-time benefits include:

• 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.