Analytical Scientist - Reagents, QC & LC-MS/SEC

The Fountain Group; Ridgefield (CT); On-site; USD 65,000 - 90,000; Full time

Job summary

The Fountain Group seeks a talented Scientist to join the Bioanalysis-Drug Metabolism/Pharmacokinetics (BA-DMPK) team at our Ridgefield, CT facility. You will support the management and characterization of reagents used in bioanalytical assays for non-clinical and clinical studies.

You will collaborate with cross-functional DMPK teams, perform routine reagent and sample handling, coordinate calibration and data archiving, and ensure safety and regulatory compliance in a fast-paced environment.

Qualifications

• Bachelor's degree in a related scientific discipline with 0-3 years with relevant experience.
• Experience with analytical size exclusion chromatography (aSEC) and LC-MS.
• Proficiency in Microsoft Office and willingness to learn electronic data management systems and laboratory software tools.

Responsibilities

• Support the management and characterization of critical reagents used in bioanalytical assays for non-clinical and clinical studies.
• Execute routine procedures related to reagents, matrices, and reference standards, including inventory management, storage, electronic tracking, and discrepancy resolution.
• Conduct analytical characterization of critical reagents, including concentration determination, aSEC and LC-MS.
• Archive analytical data, reports, and supporting documentation in electronic laboratory notebooks and present findings clearly in team meetings.
• Coordinate calibration activities and ensure safety and regulatory compliance in DMPK labs.

Skills

aSEC

LC-MS

Delivery/results

Education

Bachelor's degree in a related scientific discipline

Tools

Microsoft Office

Job description

The Fountain Group seeks a talented Scientist to join the Bioanalysis-Drug Metabolism/Pharmacokinetics (BA-DMPK) team at our Ridgefield, CT facility. You will support the management and characterization of reagents used in bioanalytical assays for non-clinical and clinical studies.

You will collaborate with cross-functional DMPK teams, perform routine reagent and sample handling, coordinate calibration and data archiving, and ensure safety and regulatory compliance in a fast-paced environment.