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Eurofins

Global lab testing and analytics network

Method Development and Validation Research Technician 1

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeLenexa, KS, USANo salary listed

About the Job

Requirements

  • A B.A. or B.S. with at least 3–4 years of method development and validation and ELISA experience, or an M.A. with at least 2–3 years of that experience, or a Ph.D. with at least 0–1 year of that experience.
  • Experience designing, validating, and/or performing immunoassays.
  • Solid ELISA experience.
  • Previous pharmaceutical, contract research organization, or clinical laboratory experience.
  • Ability to read, write, and interpret standard operating procedures, technical reports, and method protocols.
  • Authorization to work in the United States indefinitely without restriction or sponsorship.
  • Computer proficiency in Microsoft Word, Excel, and instrumentation software.
  • Ability to perform statistical analysis and data interpretation.
  • Ability to solve practical problems and troubleshoot assays.
  • Ability to manage and prioritize multiple projects effectively with little supervision.
  • Ability to work in a laboratory setting and meet the physical requirements of laboratory experiments.
  • Ability to read, write, and interpret documents such as standard operating procedures, technical reports, and method protocols.

Responsibilities

  • Develop, validate, and transfer immunoassays and bioanalytical methods, including ADA, PK, Nab, MSD, ELISA, cell-based assays, flow cytometry, and ELISpot.
  • With guidance, design, plan, perform, and manage routine and non-routine projects.
  • Assist in evaluating manufactured products and develop fit-for-purpose assays.
  • Create validation plans, test methods, worksheets, preparation sheets, and deviation reports for review by the Scientific Director.
  • Compile data and collaborate with the Scientific Director to progress projects.
  • Use information technology systems, including ERP and LIMS, as required.
  • Communicate project updates to internal teams and external clients under direction and supervision.
  • Work as a team member and independently to meet client and business deadlines.
  • Assist with assay requalification as needed.
  • Maintain regular attendance and punctuality.
  • Provide cross-functional support to other departments as needed.
  • Adjust work hours as needed to meet client deadlines.
  • Follow procedures and processes for regulatory compliance, including GxP, FDA, GLP, GDP, GCP, OECD, and CLIA requirements, and attend annual GLP training.
  • Comply with internal and customer standard operating procedures.
  • Conduct activities safely and efficiently by following site environmental health and safety requirements.
  • Perform other duties as assigned.

Desired Qualifications

  • Good communication and interpersonal skills.
  • Proven ability to compile data and create data reports.
  • Ability to multitask with good time management.
  • Ability to communicate orally and in writing with coworkers, supervisors, and clients.
  • Positive attitude and genuine interest in the drug discovery and development process and its impact on patient health.

About the Company

Eurofins

Global lab testing and analytics network

Eurofins provides global laboratory testing and analytical services to verify the safety, authenticity, and quality of products across food, water, medicine, and the environment. It operates a network of more than 900 laboratories in over 60 countries, offering access to more than 200,000 analytical methods. Its product work involves running specialized tests—using chemistry, biology, and other scientific techniques—to confirm origin, composition, and compliance of samples, such as detecting wine fraud or contaminant presence. The company differentiates itself through its massive, distributed lab network and broad portfolio, enabling standardized testing at scale and fast turnaround across many industries, rather than relying on a single specialty or location. Its goal is to protect public health and safety by delivering accurate, comprehensive testing data and helping clients meet regulatory and quality requirements.

Company size
10,001+
Company stage
IPO
Headquarters
Luxembourg
Founded
1987

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