Analytical Laboratory Associate II
About The Position
The work we do at Eurofins matters, and so do our employees. At Eurofins, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package. Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. If you’re looking for a rewarding career, apply with us today! The Analytical Laboratory Associate II will perform routine and complex physical, chemical, and instrumental analyses to support testing of protein and small‑molecule therapeutics in a GMP-regulated environment. This role requires hands-on experience with key analytical techniques—including HPLC, ICE, CGE, and UV spectroscopy—and the ability to execute testing with minimal supervision. The associate will be responsible for sample preparation, instrument operation, data documentation, and general laboratory upkeep.
Requirements
- Bachelor’s degree in Chemistry or a related scientific field, or equivalent hands-on industry experience.
- 2–3 years of experience performing bioanalytical or QC analytical testing.
- Demonstrated proficiency with HPLC, ICE, CGE, and UV spectroscopy .
- Experience working in a regulated laboratory or manufacturing environment.
- Strong understanding of Good Manufacturing Practices (GMP) .
- Familiarity with LIMS and strong data organization/documentation skills.
- Excellent attention to detail, time‑management skills, and ability to work independently within a team environment.
- Authorization to work in the United States indefinitely without restriction or sponsorship.
Responsibilities
- Perform physical, chemical, and instrumental analyses for biologic and small‑molecule samples.
- Independently operate analytical instrumentation such as HPLC , Imaged Capillary Electrophoresis (ICE) , Capillary Gel Electrophoresis (CGE) , and UV spectroscopy .
- Prepare standards, controls, and samples for analysis, ensuring accuracy and data integrity.
- Execute testing procedures with limited supervision while maintaining compliance with cGMP requirements.
- Conduct routine and monthly maintenance for analytical laboratory equipment.
- Complete laboratory support activities, including inventory management and equipment documentation.
- Accurately record and manage data within the Laboratory Information Management System (LIMS) .
- Follow established SOPs, safety guidelines, and Good Manufacturing Practices (GMP).
Benefits
- 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
- Yearly goal-based bonus & eligibility for merit-based increases
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Number of Employees
5,001-10,000 employees
