Eurofins

Method Development and Validation Research Technician I

Lenexa, KS, United States · onsite · full time

Posted October 16, 2026

Job description

The Scientist I will support the Bioanalytical Method Development and Validation Team and is responsible for the overall scientific and operational management of client bioanalytical projects supporting a variety of studies simultaneously. This role requires knowledge of method validation principles and communication skills required to transfer methods to the analytical team. Research Technician I Duties Include but are not Limited to the Following: • Performs the development, validation, and transfer of immunoassays and bioanalytical methods (including but not limited to ADA, PK, Nab, MSD, ELISA, cell-based, Flow Cytometry, and Elispot) • With guidance, designs, plans, performs, and manages routine and non-routine projects. • Assists in the evaluation of manufactured products and develops fit-for-purpose assays. • Creates technical documents in the form of validation plans, test methods, worksheets, preparation sheets, and deviation reports for review by the Scientific Director. • Compiles data and collaborates with the Scientific Director for project progression. • Applies use of IT systems (ERP, LIMs, etc.) as required. • Communicates project updates to internal team and external clients under direction supervision. • Works effectively as a member of a team as well as independently to achieve client and business deadlines. • Assists in assay re-qualification as needed. • Demonstrates and promotes the company vision. • Maintains regular attendance and punctuality. • Performs other duties as assigned. • Provides cross-functional support to other departments as needed. • Adjusts work hours as needed to meet client deadlines. • Understands and follows all procedures and processes required for work performed under Regulatory Compliance (e.g., GxP, FDA, GLP, GDP, GCP, OECD, and CLIA) and attends annual GLP training. • Complies with internal and customer SOP’s as required. • Conducts all activities in a safe and efficient manner by adhering to site environmental health and safety (EHS) requirements. Basic Minimum Education & Experience Qualifications: • B.A. or B.S. with minimum 3-4 years method development and validation & ELISA experience • M.A. with minimum 2-3 years method development and validation & ELISA experience • Ph.D. with minimum 0-1 year method development and validation & ELISA experience Basic Minimum Work Requirements: • Experience in designing, validating, and/or performing immunoassays. • Solid ELISA expereince • Previous Pharma and/or CRO, Clinical Laboratory experience required. • Ability to read, write, and interpret documents such as SOPs, technical reports, and method protocols. • Authorization to work in the United States indefinitely without restriction or sponsorship. The Ideal Candidate Possesses the Following: • Good communication and interpersonal skills. • Proven ability to compile data and create data reports. • Computer proficiency in MS Word, Excel, and instrumentation software. • Ability to perform statistical analysis and data interpretation. • Ability to solve practical problems and troubleshoot assays. • Ability to multitask with good time management. • Organizational skills to manage and prioritize multiple projects effectively under little supervision. • Proven ability to effectively communicate orally and in writing to coworkers, supervisors, and clients. • Have a positive attitude and genuine interest in the drug discovery and development process and impact to patient health. • Ability to work in a laboratory setting meeting the physical requirements of laboratory experiments. Position is full-time working Monday - Friday, 8:00am - 4:30pm, and additional hours as needed. Candidates currently living within a commutable distance to Lenexa, KS are encouraged to apply. • Location: 15 Research Park Dr., St. Charles, MO 63304 • 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 Eurofins USA Clinical Trial Solutions is a Disabled and Veteran Equal Employment Opportunity employer.