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, a place to call home, apply with us today!
Job Summary:
Perform bioassay testing and method qualification in a GMP-regulated environment, ensuring accurate documentation and data integrity.
Key Responsibilities:
Bioassay Execution:
Conduct cell-based and surrogate bioassays (e.g., ligand-binding ELISA) using plate-based formats in compliance with GMP standards.
Method Qualification & Transfer:
Support the qualification and transfer of analytical test methods to ensure consistency and reliability.
Documentation & Data Integrity:
Record laboratory activities in notebooks/e-notebooks and logbooks.
Perform data integrity checks, verification reviews, and communicate final results through electronic systems.
Education & Experience:
Bachelor’s degree in life sciences (e.g., chemistry, biology) with 4+ years of industry experience, or
MS/PhD in life sciences with 2+ years of industry experience.
Work Authorization:
Must be authorized to work in the U.S. indefinitely without restriction or a need for sponsorship.
Technical Expertise:
Experience with reporter-gene assays, cell culturing, cell counting, and cell banking.
Familiarity with GMP quality systems and lab operations.
Skills & Attributes:
Strong computer, scientific, and organizational skills.
Proficiency in Microsoft Excel, Word, PowerPoint, and related IT tools.
Excellent attention to detail and communication skills (oral and written).
Work Style:
Self-motivated, adaptable, and able to work independently or in a team setting.
Capable of learning new techniques, multitasking, and maintaining accurate records.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.
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