Senior Method Development & Validation Scientist II

Eurofins USA Clinical Trial Solutions; Lenexa (KS); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Medical benefits

Life insurance

401(k) with match

Paid vacation and holidays

Job summary

Eurofins USA Clinical Trial Solutions is seeking a Scientist II to support the bioanalytical Method Development and Validation Team. The role requires knowledge of method validation principles and the ability to transfer methods to the analytical team.

The candidate will support client projects with limited supervision, provide technical leadership, and communicate with clients directly while managing multiple studies and timelines.

Qualifications

• 5-7 years method development and validation experience.
• 3-5 years method development and validation experience with an M.A.
• 2-4 years method development and validation experience with a Ph.D.
• Pharma/CRO experience required.
• Authorization to work in the United States without sponsorship.

Responsibilities

• Works effectively as a team member to meet client and business deadlines.
• Adheres to GLP/GMP procedures and completes annual GLP training.
• Assists development, validation, and transfer of immunoassays and bioanalytical methods.
• Provides technical leadership and mentoring to junior staff.
• Communicates project updates to clients and internal teams.

Skills

Communication skills

Team collaboration

GXP/GLP knowledge

Laboratory techniques

Data analysis

Problem solving

Education

B.A./B.S. in relevant field

M.A. in relevant field

Ph.D.

Tools

MS Word

Excel

LIMS

ERP

Instrumentation software

Job description

Eurofins USA Clinical Trial Solutions is seeking a Scientist II to support the bioanalytical Method Development and Validation Team. The role requires knowledge of method validation principles and the ability to transfer methods to the analytical team.

The candidate will support client projects with limited supervision, provide technical leadership, and communicate with clients directly while managing multiple studies and timelines.