Eurofins Lancaster Laboratories

Senior Bioanalytical Chemist - Scientist II

Eurofins Lancaster Laboratories • $80K — $110K *
Saint Charles, MO 63301In-Person
Pharmaceuticals & Biotech
Less than 5 years of experience
3 weeks ago
Job Overview by Ladders

Qualifications

  • 5-7 years of experience in a lab setting, specifically with LC-MS systems.
  • Proficiency in bioanalytical method development for small and large molecules.
  • Experience in drug metabolism and metabolite identification.
  • Strong communication and interpersonal skills.
  • Ability to work under minimum supervision and take ownership of projects.
  • Experience working within a quality management system.
  • Advanced degree preferred (B.S. with 10 years, M.S. with 7 years, or Ph.D. with 3 years of relevant experience).

Responsibilities

  • Perform laboratory work and meet associated physical requirements.
  • Conduct production assays in ADME Toxicology Services and support BioTherapeutics as needed.
  • Develop LC-MS methods for ADME/DMPK applications.
  • Troubleshoot and maintain mass spectrometers and HPLC units.
  • Prepare and manage inventory of reagents and buffers for laboratory use.
  • Support validation of new methods and expand service/product offerings.
  • Communicate project updates to internal and external clients.

Benefits

  • Comprehensive medical, dental, and vision coverage.
  • Life and disability insurance.
  • 401(k) plan with company match.
  • Paid vacation and holidays.
Full Job Description
Job Description

Essential Duties and 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 will also support BioTherapeutics 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 Thermo High Resolution/ Accurate Mass 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 Qualifications (BMQ):
  • Direct/ Demonstrated experience with Liquid Chromatography- Mass Spectrometry (LC-MS) in a contract research organization or industry laboratory in one or more of the following areas:
  • Bioanalytical Method Development for Small and/or Large Molecules
  • Drug Metabolism and Metabolite Identification
  • Mass Spectrometry Based Proteomics
  • Direct/ Demonstrated experience with Liquid Chromatography- Mass Spectrometry (LC-MS) systems and troubleshooting
  • 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
  • Ability to work in the U.S. indefinitely without sponsorship

Education/Experience (BMQ):
  • B.S. with 10 years relevant experience
  • M.S. with 7 years relevant experience
  • Ph.D. with 3 years relevant experience
  • Or an equivalent of education and experience


Additional preferences:
  • Demonstrated experience with of validation of bioanalytical methods in accordance with regulatory (FDA, ICH, OECD) guidelines
  • Experience with liquid handling, automation, solid-phase extraction (SPE), HTS applications, and large-scale screening
  • Experience with Sciex® or Thermo® High Resolution/ Accurate Mass Instrumentation and Associated Software is a plus.
  • Experience in small team leadership and project management
  • Experience in leading and delivering results in R&D or innovation programs

Ability and/or Skills (BMQ):
  • 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


Additional Information

The position is full-time, Monday-Friday, 8:00 a.m.- 5:00 p.m., with overtime as needed. Candidates within a commutable distance of Saint 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

About Eurofins Lancaster Laboratories

Eurofins Lancaster Laboratories is a leading contract research organization (CRO) providing analytical, research and testing services to clients in the pharmaceutical, biopharmaceutical, biotechnology, crop protection, chemical, food, environmental and consumer products industries. The company was founded in 1961 and has grown to become one of the largest CROs in the world, with over 50 locations in 20 countries. Eurofins Lancaster Laboratories is part of the Eurofins Scientific Group, a global leader in bioanalytical testing and laboratory services. The company's services include method development and validation, stability testing, quality control testing, and regulatory compliance support.
Learn more about Eurofins Lancaster Laboratories
Size
12,000 employees
Industry
Pharmaceuticals & Biotech
* Ladders Estimates

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