Bioanalytical Method Development & Validation Tech II

Eurofins USA Clinical Trial Solutions; Lenexa (KS); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Excellent full-time benefits including

Comprehensive medical, dental, and vis

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins USA Clinical Trial Solutions is seeking a Scientist II to lead bioanalytical method development and validation for diverse client studies in Lenexa, KS. The role requires GMP/GLP knowledge, strong communication, and the ability to manage multiple projects with minimal supervision.

The candidate will mentor junior staff, transfer methods to analytical teams, and ensure timely delivery of high-quality data for clinical trials and CRO services.

Qualifications

• Requires experience with GMP/GLP in pharmaceutical/biotech settings.
• Experience designing and validating immunoassays and bioanalytical methods.
• Direct client communication and project leadership skills are essential.

Responsibilities

• Support bioanalytical method development and validation for client studies.
• Lead/mentor junior staff and provide technical leadership.
• Communicate project updates to clients and internal teams.

Skills

Communication

Data interpretation

Laboratory skills

Time management

Education

Bachelor's / Master's / PhD requirements

5-7 years method development

3-5 years method development

Tools

ERP

LIMS

MS Office

Job description

Eurofins USA Clinical Trial Solutions is seeking a Scientist II to lead bioanalytical method development and validation for diverse client studies in Lenexa, KS. The role requires GMP/GLP knowledge, strong communication, and the ability to manage multiple projects with minimal supervision.

The candidate will mentor junior staff, transfer methods to analytical teams, and ensure timely delivery of high-quality data for clinical trials and CRO services.