Lead LC-MS/MS Scientist, Clinical Assay Development

Socket.dev; Bailey (NY); On-site; USD 43,000 - 64,000; Full time

Job summary

University of Rochester is seeking a senior scientist to lead LC-MS/MS assay development and validation, driving clinical test development and lab-developed tests. You will oversee implementation, optimization, and validation within a regulated environment.

The role requires extensive LC-MS/MS experience, collaboration with clinicians and leadership, and a strong track record in regulatory compliance and innovation in diagnostic services.

Qualifications

• Bachelor's degree and 5 years of related work experience required.
• Master's degree preferred.
• PhD preferred.
• Extensive hands-on experience with LC-MS/MS-based analytical platforms including assay development, validation, optimization, troubleshooting, and implementation.

Responsibilities

• Lead development, validation, implementation, optimization, and lifecycle management of clinical LC-MS/MS assays and LDTs.
• Ensure compliance with CAP, CLIA, FDA, NYSDOH, and other regulatory standards.
• Evaluate and support new instrumentation and testing platforms to advance capabilities and efficiency.
• Serve as technical expert for LC-MS/MS and related technologies; troubleshoot complex issues.
• Support development of procedures, validation plans, training materials, and regulatory documentation.
• Collaborate with leadership, clinicians, scientists, and partners to support innovation and new test development.

Skills

LC-MS/MS troubleshooting

Analytical method development

Team leadership

Regulatory compliance

Education

Bachelor's degree

Master's degree preferred

PhD preferred

Equivalent education/experience

Tools

LC-MS/MS

Job description

University of Rochester is seeking a senior scientist to lead LC-MS/MS assay development and validation, driving clinical test development and lab-developed tests. You will oversee implementation, optimization, and validation within a regulated environment.

The role requires extensive LC-MS/MS experience, collaboration with clinicians and leadership, and a strong track record in regulatory compliance and innovation in diagnostic services.