Scientist I – Analytical Chemist

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 include, but are not limited to, the following:

• Performs work in a laboratory setting, meeting the physical job requirements of a lab role.
• Conducts production assays primarily in ADME Toxicology Services, but may support BioMAP®, Immunosignaling, Ion Channel, Biotherapeutics, and/or OncoPanel™ Services based on business needs.
• Develops Liquid Chromatography- Mass Spectrometry (LC-MS) methods for ADME/ DMPK applications in a high-throughput setting.
• Develops extraction, purification, and analytical methods supporting project teams both internally and externally for new assay development and R&D.
• Performs Troubleshooting and Maintenance of Mass Spectrometers, HPLC units, and software. Experience with Sciex®, Waters, or ThermoFisher Instrumentation is a plus.
• Prepares and manages inventory of buffers, reagents, semi-finished, and finished goods.
• Provides solutions to more complex problems, identifies and initiates process improvements
• Maintains high data quality and reproducibility.
• Performs data and report QC review within the department, and may support the Study Director.
• Takes ownership of client projects with minimal supervision.
• Supports validation of new methods and contributes to expansion of service/product line, equipment, and data management systems.
• 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 the 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

Basic Minimum Education Qualifications:

• B.S. with minimum 5 years relevant experience
• M.S. with minimum 3 years relevant experience
• Ph.D. with minimum 1 year relevant experience

 

Basic Minimum Qualifications:

• 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
• Demonstrated proficiency in High-Throughput analytical method development for small molecules.
• Direct experience with High Resolution Mass Spectrometry for large molecule analysis for ADME/DMPK/Biotherapeutics applications
• Demonstrated technical knowledge of Metabolomics in regard to pharmaceutical drug metabolism
• Demonstrated proficiency in contributing independently on a project team with time and quality deliverables
• Good communication and interpersonal skills
• Experience working in a Quality Management System Scientific expertise with mass spectrometry-based quantification for ADME/ DMPK applications in biological matrices.
• Experience with analytical method development, optimization and method transfer
• Familiarity with concepts of validation of bioanalytical methods in accordance with regulatory (FDA, ICH) guidelines
• Experience with liquid handling, automation, solid-phase extraction (SPE), HTS applications, and large-scale screening.
• Experience in small team leadership and project management
• Experience in leading and delivering results in R&D or innovation programs
• 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, and data interpretation
• Ability to multitask with organization and manage time effectively
• Ability to solve practical problems and troubleshooting skills
• Ability to work in a laboratory setting, according to the physical requirements of a laboratory role
• Lab equipment and office computer/software proficiency
• Above average oral and written communication skills
• Demonstrates a positive attitude, capacity for a team environment, and exhibits a genuine interest in drug discovery in support of advancing human health
• Ability to develop new methods and lead research and development projects
• Ability to review and QC release data/reports
• Ability to lead small, informal sub-teams, train, and train new team members
• Ability to conduct mid-size projects with minimal supervision
• Ability to contribute to strategic vision, establishment of new service lines, equipment, and data management systems
• Ability to easily support cross-functional demands

 

Position is full-time role working Monday - Friday 8:00am - 5:00pm, with overtime as needed.  Candidates currently living within a commutable distance of St. Charles, MO are encouraged to apply.

• 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

Eurofins USA Discovery Services is a Disabled and Veteran Equal Employment Opportunity employer.