LCMS Scientist

About the role

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.

Responsibilities

• 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, and/or OncoPanel™ Services based on business needs.
• Develops Liquid Chromatography-Mass Spectrometry (LC-MS) methods for ADME/DMPK applications.
• Develops analytical methods supporting project teams both internally and externally for new assay development.
• Performs troubleshooting and maintenance of Mass Spectrometers and HPLC units. Experience with Sciex® or Waters 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 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 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 Requirements:

• B.S. with minimum 5 years relevant laboratory experience
• M.S. with minimum 3 years relevant laboratory experience
• Ph.D. with minimum 1 year relevant laboratory experience
• Or an equivalent of education and laboratory experience

Basic Minimum Work Requirements:

• 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
• 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 and optimization
• 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

Skills

• Good communication and interpersonal skills
• Demonstrated proficiency in contributing independently on a project team with time and quality deliverables
• 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 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 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

Schedule

Full-time working Sunday - Thursday or Saturday - Wednesday 8:00pm - 5:00 AM.

Pay & 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