
Scientist I Analytical Chemist
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At a glance
Requirements
Credentials this posting asks for.
Job overview
Eurofins Scientific is hiring a Scientist I Analytical Chemist. The Scientist I – Analytical Chemist will support Eurofins Discovery's contract research services. This role requires applied experience and proven knowledge in analytical chemistry methods, with related experience in a contract research organization (CRO) or industry laboratory. The position involves conducting production assays, developing LC-MS methods, and performing troubleshooting and maintenance of lab equipment.
Key focus areas include Performs work in a laboratory setting, Conducts production assays primarily in ADME Toxicology Services, and Develops Liquid Chromatography- Mass Spectrometry (LC-MS) methods.
Successful candidates bring B.S. With Minimum 5 Years Relevant Laboratory Experience Or M.S. With Minimum 3 Years Relevant Laboratory Experience Or Ph.D. With Minimum 1 Year Relevant Laboratory Experience, Authorization To Work In The United States Indefinitely Without Restriction Or Sponsorship, and Direct Experience With Liquid Chromatography-Mass Spectrometry And/Or Ultraviolet Spectrometry In A CRO Or Industry Laboratory. Important skills include Analytical Chemistry Methods, Liquid Chromatography-Mass Spectrometry, ADME/DMPK Applications, Analytical Method Development, Troubleshooting Mass Spectrometers, and Maintenance Of Mass Spectrometers. Preferred (not required): ADME Toxicology...
Skills & qualifications
Skills
Qualifications
Benefits
Full job description
The Scientist I – Analytical Chemist will support the Eurofins Discovery business in contract research services. This role requires applied experience and proven knowledge in analytical chemistry methods with related experience in a contract research organization (CRO) or industry laboratory.
Scientist I Analytical Chemist Responsibilities & Duties Include but are not Limited to the Following:
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Performs work in a laboratory setting, meeting the physical job requirements of a lab role.
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Conducts production assays primarily in ADME Toxicology Services, but may support BioMAP®, Immunosignaling, Ion Channel, and/or OncoPanel™ Services based on business needs.
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Develops Liquid Chromatography- Mass Spectrometry (LC-MS) methods for ADME/ DMPK applications
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Develops analytical methods supporting project teams both internally and externally for new assay development.
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Performs Troubleshooting and Maintenance of Mass Spectrometers and HPLC units. Experience with Sciex® or Waters Instrumentation is a plus.
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Prepares and manages inventory of buffers, reagents, semi-finished and finished goods.
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Provides solutions to more complex problems, identifies and initiates process improvements
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Maintains high data quality and reproducibility.
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Performs data and report QC review within the department, and may support study director.
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Takes ownership of client projects with minimal supervision.
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Supports validation of new methods, and contributes to expansion of service/product line, equipment, and data management systems.
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Understands and complies with requirements for work performed at a GxP site.
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Completes required training and supports 100% of Employee Health and Safety requirements.
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Demonstrates proficiency with, care and maintenance of lab equipment and department assets.
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Conducts responsible use of confidential IT and business systems, as required.
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Adheres to department SOPs and documentation requirements, maintains accurate data management and reporting.
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Supports unit goals and demonstrates Eurofins’ competencies, as defined in the job plan.
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Provides training to colleagues and external end users, when required.
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Contributes to scientific community, and site research and development objectives.
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Works effectively in a team environment, under minimum direction, to achieve business production, project timelines, and quality objectives.
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Adjusts work hours and provides cross-functional support to other departments, as required, and maintains accountability in delivering to client needs/timelines.
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Routinely communicates project updates to internal and external clients.
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Performs other duties, as assigned/ Basic Minimum Education Requirements :
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B.S. with minimum 5 years relevant laboratory experience
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M.S. with minimum 3 years relevant laboratory experience
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Ph.D. with minimum 1 year relevant laboratory experience
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Or an equivalent of education and laboratory experience Basic Minimum Work Requirements :
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Direct experience with Liquid Chromatography- Mass Spectrometry and/or ultraviolet spectrometry (LC-MS or LC-UV) in a contract research organization or industry laboratory for ADME/ DMPK applications
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Experience working in a Quality Management System
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Scientific expertise with mass spectrometry-based quantification for ADME/ DMPK applications in biological matrices.
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Experience with analytical method development and optimization
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Familiarity with concepts of validation of bioanalytical methods in accordance with regulatory (FDA, ICH) guidelines
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Experience with liquid handling, automation, solid-phase extraction (SPE), HTS applications, and large-scale screening
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Experience in small team leadership and project management
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Experience in leading and delivering results in R&D or innovation programs
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Authorization to work in the United States indefinitely without restriction or sponsorship. The Ideal Candidate Possesses the Following:
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Good communication and interpersonal skills
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Demonstrated proficiency in contributing independently on a project team with time and quality deliverables
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Ability to read, write, and interpret documents, such as standard operating procedures and technical reports
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Ability to perform mathematical calculations, statistical analyses, and data interpretation
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Ability to multitask with organization and manage time effectively
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Ability to solve practical problems and troubleshooting skills
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Ability to work in a laboratory setting, according to physical requirements of a laboratory role
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Lab equipment and office computer/software proficiency
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Above average oral and written communication skills
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Demonstrates a positive attitude, capacity for team environment, and exhibits a genuine interest in drug discovery in support of advancing human health
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Ability to develop new methods, and lead research and development projects
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Ability to review and QC release data/reports
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Ability to lead small, informal sub-teams, train, and train new team members
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Ability to conduct mid-size projects with minimal supervision
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Ability to contribute to strategic vision, establishment of new service lines, equipment, and data management systems
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Ability to easily support cross-functional demands Position is full-time working Sunday - Thursday or Saturday - Wednesday 8:00pm - 5:00 PM . Candidates currently living within a commutable distance of St. Charles, MO are encouraged to apply.
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Excellent full-time benefits including comprehensive medical coverage, dental, and vision options
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Life and disability insurance
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401(k) with company match
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Paid vacation and holidays Eurofins USA Discovery Services is a Disabled and Veteran Equal Employment Opportunity employer.
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