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Senior Clinical Lc/Ms Scientist

Company

Kelly

Address Kansas City Metropolitan Area, United States
Employment type FULL_TIME
Salary
Category Biotechnology Research,Hospitals and Health Care
Expires 2023-08-14
Posted at 9 months ago
Job Description

Kelly® Science & Clinical is seeking a Senior LC/MS Scientist for a direct-hire opportunity with one of our clients, a CLIA-certified clinical diagnostics lab in the Kansas City area. If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.


Overview

The incumbent will join a growing team and lead the development and validation of laboratory-developed tests (LDTs). The ideal candidate will have extensive experience with LC/MS instrumentation and methods, a strong background in analytical chemistry and molecular biology, and a demonstrated track record of developing LDTs from start to finish.


Responsibilities

  • Optimize assay parameters such as sample preparation, chromatography, and mass spectrometry conditions to achieve high sensitivity, specificity, and accuracy.
  • Stay current with the latest developments in LC/MS technology, regulatory requirements, and industry trends.
  • Collaborate with cross-functional teams to support research and development projects and ensure timely completion of deliverables.
  • Design and develop LC/MS-based assays for the detection and quantification of target analytes in biological specimens (urine, blood, and saliva).
  • Maintain and troubleshoot LC/MS instrumentation and software.
  • Analyze and interpret LC/MS data to generate accurate and reliable results.
  • Validate assay performance according to CAP LDT standards.
  • Document and communicate experimental procedures, results, and conclusions to internal and external stakeholders.


Qualifications

  • Commitment to quality, safety, and compliance with laboratory standards and protocols
  • Understanding of regulatory requirements for LDTs, including CLIA, CAP, and ISO guidelines.
  • Process-driven approach to development with strong analytical and problem-solving skills, with attention to detail and accuracy.
  • Hands-on experience with LC/MS instrumentation and software, including mass spectrometers, HPLC systems, and data processing tools.
  • Excellent verbal and written communication skills, with the ability to collaborate effectively with interdisciplinary teams.
  • Minimum of 3-5 years of experience in LC/MS-based assay development and validation
  • Demonstrated ability to work independently and manage multiple projects simultaneously, while meeting committed timelines.
  • Master's or Ph.D. or equivalent degree in analytical chemistry or biochemistry


What happens next:

Once you apply, you’ll proceed to the next steps if your skills and experience look like a good fit. But don’t worry – even if this position doesn’t work out, you’re still in our network. That means our team of expert Science & Clinical recruiters will have access to your profile, making your opportunities limitless.

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