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Method Development and Validation Research Technician I (Bioanalytical Methods)

Формат работы
onsite
Тип работы
fulltime
Грейд
junior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Method Development and Validation Research Technician I (Bioanalytical Methods): Developing, validating, and transferring immunoassays and bioanalytical methods for client pharmaceutical and clinical projects with an accent on ADA, PK, Nab, MSD, ELISA, cell-based assays, flow cytometry, and Elispot. Focus on designing studies, compiling and interpreting data, troubleshooting assays, preparing technical documentation, and maintaining GxP-compliant laboratory work.

Location: Lenexa, Kansas, USA; candidates must live within a commutable distance. The posting also lists a worksite at 15 Research Park Dr., St. Charles, Missouri. The role is laboratory-based and requires Monday–Friday attendance from 8:00 a.m. to 4:30 p.m., with additional hours as needed.

Company

Eurofins Scientific provides analytical testing, contract research, clinical, pharmaceutical, food, environmental, and life sciences services through an international laboratory network.

What you will do

  • Develop, validate, transfer, and re-qualify 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 client projects under guidance.
  • Evaluate manufactured products and develop fit-for-purpose assays.
  • Prepare validation plans, test methods, worksheets, preparation sheets, deviation reports, data reports, and other technical documentation.
  • Compile data, perform statistical analysis, interpret results, troubleshoot assays, and communicate project updates to internal teams and clients.
  • Follow applicable regulatory, safety, environmental, and customer SOP requirements, including GxP, FDA, GLP, GDP, GCP, OECD, and CLIA standards.

Requirements

  • B.A. or B.S. with 3–4 years of method development and validation experience; or M.A. with 2–3 years; or Ph.D. with 0–1 year.
  • Experience designing, validating, and/or performing immunoassays.
  • 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 is required.
  • Proficiency with MS Word, Excel, instrumentation software, data interpretation, problem-solving, multitasking, and laboratory work.

Culture & Benefits

  • Full-time Monday–Friday schedule with additional hours when needed to meet client deadlines.
  • Medical, dental, and vision coverage.
  • Life and disability insurance.
  • 401(k) plan with company match.
  • Paid vacation and holidays.

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