Analytical Chemistry Data Reviewer

About the role

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. Life at Eurofins is a meritocracy, where people are empowered to make decisions and are rewarded for their success, allowing them to advance quickly. Become your most extraordinary self with support and development throughout your career.

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.

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
• 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
• 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

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

Benefits

• 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

Pay

Compensation: $26.25 - $30.00 per hour

Schedule

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