Scientists (LCMS-MS Bioanalysis & Method Validation)

IQVIA•Ithaca, NY

12d•$41,400 - $108,000•Onsite

About The Position

IQVIA Laboratories in Ithaca, NY has multiple Scientist opportunities open across LC–MS bioanalysis and method validation teams. Apply to this posting if you’re interested in Scientist roles focused on generating high-quality data for both large and small molecule workflows in a regulated laboratory environment.

Requirements

Bachelor's Degree in applied/laboratory sciences or a relevant scientific discipline with direct laboratory coursework
Hands-on experience with LC–MS workflows including operation of Triple Quadrupole and/or high resolution mass spectrometers, UPLC systems, calibration and tuning, and data interpretation.
Knowledge of sample handling and preparation techniques (e.g., protein precipitation, SPE, immunocapture) and familiarity with GLP documentation standards
Strong attention to detail and commitment to producing high-quality, compliant data and documentation to timelines
Ability to troubleshoot complex experiments and laboratory equipment, clearly present findings, and know what to escalate versus address independently
Effective communication and interpersonal skills in a collaborative team environment, including working with project teams and cross-functional stakeholders

Nice To Haves

experience preparing data for LIMS (e.g., Watson) is a plus

Responsibilities

Follow all applicable health, safety, and regulatory standards while performing laboratory work
Design, set up, and execute qualitative and quantitative experiments to support LC–MS bioanalysis, method validation, and downstream sample analysis
Prepare, extract, and process samples using techniques such as protein precipitation, solid-phase extraction, and immunocapture as applicable to the assay
Operate, calibrate, tune, and optimize LC–MS instrumentation (including Triple Quadrupole mass spectrometers and UPLC systems) and perform routine maintenance and troubleshooting per SOPs
Review, interpret, integrate, and summarize chromatographic and mass spectrometry data; identify data abnormalities and initiate appropriate troubleshooting studies using sound scientific judgment
Prepare documentation and deliverables including protocols, technical summaries and reports, GLP-compliant laboratory notebook entries, and data packages for project outcomes
Collaborate with Project Management and cross-functional stakeholders to plan work, communicate progress, and meet study objectives within tight timelines
Contribute to continuous improvement by helping evaluate new technologies and techniques and supporting process improvements within the lab