Analytical Chemistry Data Review (Chemistry Background Required)
About The Position
At Eurofins PSS, we partner with leading international companies in the pharma, medical device, food, cosmetic, and consumer products industries, providing mission-critical testing services. As part of Eurofins Scientific, an international life sciences company with a vast network of laboratories and employees, we offer a meritocratic environment where individuals are empowered to make decisions and advance quickly. This role involves reviewing GMP data generated by testing personnel to ensure compliance with governing procedures, verifying logbook entries, confirming sample chain of custody, and reviewing audit trails. The position also requires clear communication with testing personnel to resolve discrepancies, partnering with laboratory staff for continuous improvement, and accurately documenting activities using Good Documentation Practices (GDP). Additionally, the role includes conducting laboratory safety and compliance walkthroughs and completing all required trainings.
Requirements
- Bachelor’s degree (BS) in Chemistry, Life Sciences, or a related scientific discipline
- 1–2 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
Benefits
- Comprehensive medical coverage
- Dental options
- Vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation
- Paid holidays
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
