Senior MS Scientist — Absolute Quantification & Innovation

Molecularyou

Vancouver

On-site

CAD 120,000 - 180,000

Full time

14 days+
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Benefits offered by this job

Competitive salary
Extended health, dental, vision
Equity participation
Learning budget
Flexible work environment

Job summary

Molecular You is seeking a Senior Mass Spectrometry Scientist to lead assay development and absolute quantification in clinical matrices, driving ISO-compliant deployment and QA. You will optimize LC-MS/MS workflows, validate methods, and mentor junior scientists in a regulated environment.

You will collaborate with bioinformaticians, product and medical teams to translate rigorous analytics into clinical impact, while advancing next-generation MS capabilities and maintaining audit-ready

Qualifications

  • PhD or MSc with 5+ years industry experience in quantitative MRM-MS.
  • Expertise with absolute quantification using stable isotope-labeled standards.
  • Experience working with LIMS and regulated laboratories.
  • Strong troubleshooting across chromatography, ionization, and detection.
  • Experience with method validation under FDA/CLIA/ISO guidelines.

Responsibilities

  • Develop, validate, and oversee proprietary MRM-MS assays for absolute quantification in clinical matrices.
  • Lead method validation packages per FDA Bioanalytical Method Validation, CLIA and ISO 15189.
  • Maintain SOPs to ensure robust, auditable workflows.
  • Create training transfer packages for partner laboratories to run assays reliably.
  • Develop MS-based technologies for integration into the clinical workflow.
  • Mentor junior scientists and collaborate with cross-functional teams.

Skills

MRM-MS
LC-MS/MS instrumentation
Quantitative analysis
SOPs & QA
Mentoring
Regulatory knowledge

Education

PhD in Analytical Chemistry
MSc with 5+ years exp

Tools

Agilent LC-MS/MS
Sciex LC-MS/MS
Thermo LC-MS/MS
Waters LC-MS/MS

Job description

Molecular You is seeking a Senior Mass Spectrometry Scientist to lead assay development and absolute quantification in clinical matrices, driving ISO-compliant deployment and QA. You will optimize LC-MS/MS workflows, validate methods, and mentor junior scientists in a regulated environment.

You will collaborate with bioinformaticians, product and medical teams to translate rigorous analytics into clinical impact, while advancing next-generation MS capabilities and maintaining audit-ready

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