Method Development and Validation Research Technician I

Eurofins•Lenexa, KS

5d•Onsite

About The Position

The Research Technician I supports the Bioanalytical Method Development and Validation Team and contributes to the scientific and operational management of client bioanalytical projects across multiple studies. The role involves developing, validating, and transferring immunoassays and other bioanalytical methods, preparing technical documentation, compiling data, and communicating project updates under supervision. The technician works with internal teams and clients while meeting project deadlines and following applicable regulatory, safety, and company procedures. The position is full-time, Monday through Friday, 8:00 a.m. to 4:30 p.m., with additional hours as needed. Candidates living within commuting distance of Lenexa, Kansas, are encouraged to apply.

Requirements

Bachelor of Arts or Bachelor of Science with at least 3–4 years of method development and validation and ELISA experience; or Master of Arts with at least 2–3 years; or Ph.D. with at least 0–1 year.
Experience designing, validating, and/or performing immunoassays.
Solid ELISA experience.
Previous pharmaceutical, CRO, or clinical laboratory experience.
Ability to read, write, and interpret SOPs, technical reports, and method protocols.
Authorization to work indefinitely in the United States without restriction or sponsorship.
Ability to work in a laboratory setting and meet the physical requirements of laboratory experiments.

Nice To Haves

Good communication and interpersonal skills.
Ability to compile data and create data reports.
Computer proficiency in MS Word, Excel, and instrumentation software.
Ability to perform statistical analysis and interpret data.
Ability to solve practical problems and troubleshoot assays.
Ability to multitask and manage time effectively.
Organizational skills to manage and prioritize multiple projects with little supervision.
Effective oral and written communication with coworkers, supervisors, and clients.
Positive attitude and genuine interest in drug discovery and development and its impact on patient health.

Responsibilities

Develop, validate, and transfer immunoassays and bioanalytical methods, including ADA, PK, Nab, MSD, ELISA, cell-based assays, Flow Cytometry, and Elispot.
Design, plan, perform, and manage routine and non-routine projects with guidance.
Assist in evaluating manufactured products and develop fit-for-purpose assays.
Prepare technical documents, including validation plans, test methods, worksheets, preparation sheets, and deviation reports, for review by the Scientific Director.
Compile data and collaborate with the Scientific Director on project progression.
Use IT systems such as ERP and LIMS as required.
Communicate project updates to internal teams and external clients under direct supervision.
Work independently and as part of a team to meet client and business deadlines.
Assist with assay re-qualification as needed.
Demonstrate and promote the company vision; maintain regular attendance and punctuality.
Perform other assigned duties and provide cross-functional support to other departments as needed.
Adjust work hours as needed to meet client deadlines.
Follow procedures and processes for work under regulatory compliance, including GxP, FDA, GLP, GDP, GCP, OECD, and CLIA; attend annual GLP training.
Comply with internal and customer SOPs.
Follow site environmental health and safety requirements and conduct work safely and efficiently.