Overview In this role you support Eurofins Discovery in contract research, applying analytical chemistry expertise to ADME/DMPK-focused projects. You work within a cross-functional team to develop LC-MS methods, troubleshoot instruments, and deliver high-quality data for client projects. You contribute to method validation, data integrity, and continuous process improvements while operating in a GxP-regulated environment. This is a hands-on, growth-focused position in a well-established CRO setting that shapes analytical capabilities for drug discovery.
Compensation / Benefits- comprehensive medical coverage, dental and vision
- life and disability insurance
- 401(k) with company match
- paid vacation and holidays
Responsibilities- Develops LC-MS methods for ADME/DMPK applications and supports new assay development
- Performs instrument maintenance and troubleshooting for MS and HPLC systems
- Prepares and manages buffers, reagents, and finished goods inventory
- Ensures data quality and reproducibility; conducts data/ QC review
- Owns client projects with minimal supervision and supports study directors
- Contributes to validation of new methods and expansion of service lines
- Adheres to GxP requirements and completes safety trainings
- Trains colleagues and external end users as needed
- Communicates project updates to internal and external clients
Key requirements- Direct LC-MS and/or LC-UV experience in a CRO or industry lab for ADME/DMPK
- Experience in quality management systems
- Mass spectrometry-based quantification in biological matrices
- Analytical method development and optimization
- Validation concepts per FDA/ICH guidelines
- Experience with sample handling, automation, SPE, HTS, and large-scale screening
- Leadership or project management experience in R&D
- Authorization to work in the US without sponsorship
- strong communicator
- independence with time and quality deliverables
- team-oriented and collaborative
- LC-MS
- HPLC
- UL/UV (LC-UV)
