Senior Director, LCMS Platforms & Large-Molecule Bioanalysis

Top Quality Recruitment (TQR)

Pleasanton (CA)

On-site

USD 180,000 - 260,000

Full time

3 days ago
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Job summary

Top Quality Recruitment (TQR) seeks a Director of LCMS Platforms to build and lead the LCMS function in a GLP/GCLP compliant bioanalytical lab. You will oversee assay development, validation, and study execution while driving scientific strategy and client satisfaction.

The role requires a PhD or Master’s, 10+ years in bioanalysis/LCMS, and a proven track record in large-molecule bioanalysis, FDA/EMA regulatory familiarity, and leadership of cross-functional teams.

Qualifications

  • PhD or Master’s in biology, immunology, chemistry or related field.
  • Minimum 10 years in bioanalysis, biomarkers, or LCMS method development.
  • Strong expertise in bioanalytical assays including PK/PD and regulatory guidance.
  • Experience developing LCMS methods for large-molecule biotherapeutics.

Responsibilities

  • Lead and manage supervisors and scientists in bioanalytical assay development and validation.
  • Oversee large-molecule LCMS studies to ensure GLP/GCLP compliance.
  • Develop, validate, troubleshoot LCMS methods for biological samples.
  • Review regulatory documents and data packages; manage timelines.
  • Mentor team members and present data to clients and internal teams.
  • Drive innovation through new tech, instrumentation, and strategies.

Skills

ADC bioanalysis
Leadership & PM
Communication
Independent work

Education

PhD or Master’s in biology/chemistry
10+ years bioanalysis/LCMS
Regulatory familiarity (FDA/EMA/ICH)

Job description

Top Quality Recruitment (TQR) seeks a Director of LCMS Platforms to build and lead the LCMS function in a GLP/GCLP compliant bioanalytical lab. You will oversee assay development, validation, and study execution while driving scientific strategy and client satisfaction.

The role requires a PhD or Master’s, 10+ years in bioanalysis/LCMS, and a proven track record in large-molecule bioanalysis, FDA/EMA regulatory familiarity, and leadership of cross-functional teams.

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