Associate Scientist II

Company Description

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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

In 2024, Eurofins generated total revenues of EUR € 6,515 billion, and has been among the best performing stocks in Europe over the past 20 years.

Job Description

Associate Scientist II responsibilities include, but are not limited to, the following:

• Performs work in a laboratory setting, meeting the physical job requirements of a lab role
• Prepares and manages inventory of buffers, reagents, media, semi-finished goods, and finished goods
• Maintains cell culture in a BSL2 laboratory, and adheres to cleanroom guidelines and aseptic technique, according to protocol
• Conducts production assays in ADMET, Ion Channels, Immunosignaling, OncoPanel™ Services, BioMAP®, and manufacturing, lot release assays and inventory management for Cell Products
• Runs high throughput ELISA and other microwell plate based assays
• Runs and performs routine maintenance of automation systems
• Provides solutions to more complex problems, identifies and initiates process improvements
• Performs data and reports QC review within the department
• Takes ownership of small laboratory or research and development projects with minimal supervision
• Understands and complies with requirements for work performed at a GxP site
• Completes required training and supports 100% of Employee Health and Safety requirements
• Demonstrates proficiency with, care and maintenance of lab equipment and department assets
• Conducts responsible use of confidential IT and business systems, as required
• Adheres to department SOPs and documentation requirements, maintains accurate data management and reporting
• Supports unit goals and demonstrates Eurofins’ competencies, as defined in the job plan
• Provides training to colleagues and external end users, when required
• Contributes to scientific community, and site research and development objectives
• Works effectively in a team environment, under minimum direction, to achieve business production, project timelines, and quality objectives
• Adjusts work hours and provides cross-functional support to other departments, as required, and maintains accountability in delivering to client needs/timelines
• Routinely communicates project updates to internal and external clients
• Performs other duties, as assigned

Qualifications

Basic Minimum Education Qualifications:

• B.A. or B.S. with 2 years of relevant experience
• M.A. or M.S. with 1 year of relevant experience

Basic Minimum Qualifications:

• Experience with ELISA or other microwell plate based assay execution
• Experience in a contract research organization
• Experience with automation/HTS applications and large-scale screening
• Experience with automated liquid handling workstations
• Programming experience is a plus
• Authorization to work in the United States indefinitely without restriction or sponsorship.

The Ideal Candidate Possesses the Following:

• Ability to read, write, and interpret documents, such as standard operating procedures and technical reports
• Ability to perform mathematical calculations, statistical analyses,