Eurofins Panlabs is committed to assisting clients achieve drug discovery success by providing comprehensive data. We are the most experienced pharmacology service company, in continuous operation for over 40 years, while setting the benchmarks for quality, convenience, and expertise. Our legacy includes: concurrent controls run with every experiment, a historical database on assay performance, industry experienced professionals that assist in study design and data interpretation, and eCTD compatible data reports.
Eurofins Panlabs is searching for an Associate Scientist III to work in St. Charles, MO.
Associate Scientist III 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 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 Channel, Immunosignaling, OncoPanelTM Services, and manufacturing, lot release assays and inventory management for Cell Products
Provides solutions to more complex problems, identifies and initiates process improvements
Performs data and report QC review within the department
Takes ownership of mid-size laboratory or research and development 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
The ideal candidate would possess :
Experience in a contract research organization Experience with method development and optimization Experience with automation /HTS applications Experience in small team leadership and project management
Experience in leading and delivering results in R&D
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 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
Basic Minimum Qualifications :
B.A. or B.S. with 3 years of relevant experience M.A. or M.S. with 2 years of relevant experience
Direct experience with cell-based assays
Demonstrated proficiency in contributing independently on a project team with time and quality metrics
Good communication and interpersonal skills
Authorization to work in the United States indefinitely without restriction or sponsorship
Position is full-time, Monday-Friday, 8 a.m.-5 p.m., with overtime as needed. Candidates currently living within a commutable distance of St. Charles, MO are encouraged to apply.
As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays and vacation, personal days, and dental and vision options.
To learn more about Eurofins, please explore our website www.eurofinsus.com .
Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
