GMP Analytical Chemistry Data Reviewer

About the role

Eurofins PSS works with leading international companies across the pharma, medical device, food, cosmetic & consumer products industries, providing mission-critical testing. For 20 years, our international network of teams has served clients at their sites across 20 countries. PSS® is part of Eurofins Scientific, an international life sciences company offering a unique range of analytical testing services across multiple industries through a network of over 950 laboratories in 60 countries and approximately 63,000 employees. Life at Eurofins is a meritocracy where people are empowered to make decisions and are rewarded for their success, enabling rapid career advancement with support and development throughout your tenure.

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 Good Documentation Practices (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
  • 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.
• 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.

Schedule

Full Time, Monday–Friday, First Shift, 8:00 am–4:30 pm.

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

$26.25 – $30.00 per hour.