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Assay Validation Scientist Assay Validation Scientist Eurofins In-person · Lenexa, KS, US about

Job in Lenexa, Johnson County, Kansas, 66215, USA
Listing for: Seeds Renewables
Full Time position
Listed on 2026-06-08
Job specializations:
  • Science
    Research Scientist, Clinical Research, Medical Science
  • Healthcare
    Clinical Research, Medical Science
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below
Position: Assay Validation Scientist Assay Validation Scientist Eurofins In-person · Lenexa, KS, US about[...]

Assay Validation Scientist

Include but are not Limited to the Following:

The Assay Validation Scientist is primarily responsible for conducting the successful and efficient transfer of technology into the laboratory including method/assay validation execution to meet corporate/client timelines and cost objectives.

Level I – Minimum
  • Learn new techniques and instrumentation
  • Implement assay validation plans, design, and protocols
  • Operate, calibrate and maintain all laboratory equipment and instruments according to standard operating procedures to ensure quality results
  • Keep accurate documentation of all validation project steps according to Eurofins Viracor regulatory guidelines
  • Compose and analyze validation data
  • Perform peer review of documentation and data
  • Assist in writing validation protocols, validation reports, standard operating procedures and study-specific work instructions
  • Participate in quality assurance/quality improvement activities. Follow all QC guidelines as stated in the Procedure Manual
  • Disposes of bio-hazardous materials, chemical waste, sharp and other potentially hazardous materials according to Policy
  • Accurate pipetting and bench-level skills (i.e., pipette standard curves to within accurate limits stated in procedure manual)
  • Other duties as assigned by management
Level II – Fully meets the responsibilities of Level I plus the following
  • Write standard operating procedures and study-specific work instructions with minimal assistance
  • Write validation plans and reports with minimal assistance
  • Assist on establishing clear timelines per assigned projects and coordinate scheduling
  • Proficient in multiple platforms and supporting applications
  • Ability to successfully multitask more than one assignment at a given time
  • Prepare data for presentation at scientific meetings or for client presentations
Level III – Fully meets the responsibilities of Level II plus the following
  • Lead design and execution of validation projects with little to no assistance from senior management
  • Analyze and interpret data independently
  • Independently devise/write validation plans and project reports
  • Obtain advanced knowledge of Viracor Eurofins standard operating procedures, assays, and instrumentation
  • Instruct other scientists and lead their development
  • As appropriate, communicate with clients within project meetings or independently via email or teleconference
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