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Eurofins USA Clinical Trial Solutions
Method Development and Validation Research Technician IEurofins USA Clinical Trial Solutions • Lenexa, Kansas, United States
Method Development and Validation Research Technician I

Method Development and Validation Research Technician I

Eurofins USA Clinical Trial Solutions • Lenexa, Kansas, United States
5 days ago
Job type
  • Full-time
Job description

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.


Qualifications

Basic Minimum Education & Experience Qualifications:

  • B.A. or B.S. with minimum 3-4 years method development and validation experience
  • M.A. with minimum 2-3 years method development and validation experience
  • Ph.D. with minimum 0-1 year method development and validation experience

Basic Minimum Work Requirements:

  • Experience in designing, validating, and/or performing immunoassays.
  • 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.



Additional Information

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.

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Method Development and Validation Research Technician I • Lenexa, Kansas, United States

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