Analytical Chemistry Data Review (Chemistry Background Required)

Eurofins USA PSS Insourcing Solutions•Rensselaer, NY

1d•Onsite

About The Position

Eurofins PSS is seeking an Analytical Chemistry Data Reviewer with a strong chemistry background to join their team. This role involves reviewing GMP data and documentation to ensure compliance with governing procedures, logbook standards, sample chain of custody, and audit trail requirements. The position requires clear communication with testing personnel to resolve discrepancies and a collaborative approach to support compliance and continuous improvement. The role also includes conducting laboratory safety and compliance walkthroughs and completing all required training.

Requirements

Bachelor’s degree (BS) in Chemistry, Life Sciences, or a related scientific discipline.
2-3 years of cGMP experience in a regulated laboratory environment.
Hands-on experience with HPLC/UPLC and UV‑Vis spectrophotometry.
Proficiency in processing and reviewing quantitative liquid chromatography data.
Strong computer literacy and organizational abilities.
Excellent written and verbal communication skills with high attention to detail.
Demonstrated integrity, professionalism, and strong work ethic.
Ability to work independently as well as collaboratively within a team.
Self‑motivated, adaptable, and maintains a positive attitude in a fast‑paced environment.
Capable of meeting physical demands, including lifting 25 lbs. or more, prolonged standing or walking, pushing/pulling carts or equipment, and bending or reaching for supplies.
Ability to learn new processes, manage multiple tasks simultaneously, and maintain accurate records.
Ability to follow instructions and comply with company policies and regulatory requirements.
Authorized to work in the United States indefinitely without restriction or sponsorship.

Nice To Haves

Experience with ELISA, MCE, and/or iCIEF techniques.

Responsibilities

Review GMP data generated by testing personnel to ensure compliance with governing procedures.
Verify logbook entries for completeness, accuracy, and adherence to GDP standards.
Confirm sample chain of custody integrity throughout testing activities.
Review audit trails to ensure actions executed align with procedural requirements and timelines.
Communicate clearly and efficiently with testing personnel to resolve annotations, discrepancies, or corrections.
Partner with laboratory staff to support compliance and continuous improvement.
Accurately document activities in logbooks, laboratory notebooks, and electronic systems using GDP principles.
Conduct laboratory safety and compliance walkthroughs, documenting observations as required.
Complete all required safety, procedural, and refresher trainings on time.