Analytical Chemistry Data Review (Chemistry Background Required) at Eurofins

Rensselaer, New York, United States -

Full Time

Start Date

Immediate

Expiry Date

20 Jul, 26

Salary

23.5

Posted On

21 Apr, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Analytical chemistry, GMP data review, HPLC, UPLC, UV-Vis spectrophotometry, ELISA, MCE, iCIEF, Data integrity, GDP, Laboratory safety, Documentation, Compliance, Quantitative analysis, Computer literacy, Attention to detail

Industry

Medical and Diagnostic Laboratories

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. 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. Job Description GMP Data & Documentation Review 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 Communication & Issue Resolution Communicate clearly and efficiently with testing personnel to resolve annotations, discrepancies, or corrections Partner with laboratory staff to support compliance and continuous improvement Good Documentation Practices (GDP) Accurately document activities in logbooks, laboratory notebooks, and electronic systems using GDP principles Safety & Compliance Conduct laboratory safety and compliance walkthroughs, documenting observations as required Complete all required safety, procedural, and refresher trainings on time Qualifications Education & Experience Bachelor’s degree (BS) in Chemistry, Life Sciences, or a related scientific discipline 1–2 years of cGMP experience in a regulated laboratory environment Technical Skills Hands-on experience with HPLC/UPLC and UV‑Vis spectrophotometry Experience with ELISA, MCE, and/or iCIEF techniques preferred Proficiency in processing and reviewing quantitative liquid chromatography data Professional Skills Strong computer literacy and organizational abilities Excellent written and verbal communication skills with high attention to detail Demonstrated integrity, professionalism, and strong work ethic Work Style & Physical Requirements 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 Additional Requirements 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 Additional Information Position is Monday- Friday, 8:30 AM -4:30 PM. Overtime as needed. Pay range: $22.50 - $23.50/hour Excellent full-time benefits, including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer. Compensation: USD 22.50 - USD 23.50 - hourly

Responsibilities

The role involves reviewing GMP data and documentation to ensure compliance with procedural requirements and regulatory standards. You will also collaborate with laboratory staff to resolve discrepancies and maintain sample chain of custody integrity.