Senior LC-MS Bioanalytical Scientist (GLP/ADC)

Actalent

Washington

On-site

USD 120,000 - 190,000

Full time

14 days+
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Job summary

Actalent is seeking an LC-MS Principal Research Scientist to lead pre-clinical GLP bioanalytical method development, validation, and sample analysis using triple quadrupole LC‑MS/MS. The role covers small and large molecules, ADCs, and complex workflows, with direct technical leadership and client-facing collaboration.

You will ensure GLP compliance, generate high‑quality reports, and supervise lab activities in a fast‑paced, teamwork‑driven environment.

Qualifications

  • Bachelor’s degree in Immunology, Biology, Chemistry or related field.
  • Minimum 5 years GLP laboratory experience in bioanalytical science.
  • Experience with LC-MS/MS in a CRO or bio/pharma setting.
  • Strong documentation skills ensuring data integrity (ALCOA+).
  • Experience with triple quadrupole LC-MS systems for method development.
  • Ability to work under GLP, FDA ICH guidelines and SOPs.

Responsibilities

  • Lead method development and validation for small and large molecule analysis using LC‑MS/MS.
  • Act as SME for pre‑clinical GLP studies and ADC/large molecule workflows.
  • Collaborate with clients and internal teams to deliver quality reports.
  • Ensure compliance with GLP, SOPs, and QA requirements across studies.
  • Prepare study documentation and maintain chain of custody for samples.
  • Provide scientific leadership and supervision of laboratory activities.
  • Assist with instrument calibration, maintenance, and data collection.
  • Communicate updates to clients through calls and reports.

Skills

LC-MS/MS analysis
GLP compliance
Triple quadrupole LC-MS/MS
ADCs & large molecules
Documentation ALCOA+
Client communication

Education

Bachelor’s in Immunology, Biology, or Chemistry

Tools

Shimadzu LC-MS
SCIEX LC-MS/MS
Watson LIMS / data management

Job description

Actalent is seeking an LC-MS Principal Research Scientist to lead pre-clinical GLP bioanalytical method development, validation, and sample analysis using triple quadrupole LC‑MS/MS. The role covers small and large molecules, ADCs, and complex workflows, with direct technical leadership and client-facing collaboration.

You will ensure GLP compliance, generate high‑quality reports, and supervise lab activities in a fast‑paced, teamwork‑driven environment.

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