Method Development Scientist I

Labcorp•Madison, WI

1d•$70,000 - $85,000•Onsite

About The Position

In this role, you will support the development, transfer, troubleshooting, and documentation of sensitive and reliable LC-MS/MS bioanalytical methods for the analysis of pharmaceuticals and related compounds in biological matrices. You will apply scientific principles, regulatory awareness, and hands-on laboratory expertise to generate high-quality data and support internal and external communications while contributing to process improvements. No significant remote work or travel and does include direct client interaction. This is an individual contributor role in a regulated lab environment. Develops routine and complex analytical methods for quantitation of pharmaceuticals from biological matrices, applying troubleshooting and documentation practices. Supports method development and method transfer activities, including method writing and associated laboratory work. Supports troubleshooting across development, validation, and sample analysis. Maintains complete, accurate, and timely documentation in accordance with SOPs, GLP, and regulatory requirements. Supports data-driven decision-making by communicating method performance, risks, and resource needs. Serves as a technical resource within the group, assisting with troubleshooting and training as appropriate. Participates in client interactions and internal cross-functional collaborations. Contributes to evaluation of departmental procedures and local process improvements. Promotes a cohesive and collaborative team environment.

Requirements

Bachelor’s degree (Chemistry, Biochemistry, etc.)
4 years or more of analytical laboratory experience
4 years or more of LC-MS/MS experience
Demonstrated communication skills (external publications and presentations)
Client management experience
Proven ability to prioritize and manage time
Excellent attention to detail

Nice To Haves

Doctoral degree (Chemistry, Biochemistry, etc.)
Bioanalytical experience
Any version of GLP/GMP/GCP/SOP experience helpful
Method development exposure

Responsibilities

Develops routine and complex analytical methods for quantitation of pharmaceuticals from biological matrices, applying troubleshooting and documentation practices.
Supports method development and method transfer activities, including method writing and associated laboratory work.
Supports troubleshooting across development, validation, and sample analysis.
Maintains complete, accurate, and timely documentation in accordance with SOPs, GLP, and regulatory requirements.
Supports data-driven decision-making by communicating method performance, risks, and resource needs.
Serves as a technical resource within the group, assisting with troubleshooting and training as appropriate.
Participates in client interactions and internal cross-functional collaborations.
Contributes to evaluation of departmental procedures and local process improvements.
Promotes a cohesive and collaborative team environment.