Chief, Central Analytical Lab & Technology Platform

Takeda

Lexington (MA)

Vor Ort

USD 200.000 - 333.000

Vollzeit

vor 15 Stunden
Sei unter den ersten Bewerbenden
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Zusammenfassung

Takeda seeks an accomplished pharma analytics leader to head its US central laboratory (Lexington, MA) and a Japan vaccines testing lab. You will steward GMP method performance, data integrity, and resource planning across modalities, ensuring strategic priority alignment with portfolio and quality standards.

The role requires 20+ years in pharma/biotech analytical development or QC, strong people leadership, and a track record of deploying new analytical tech, automation, and advanced analytics

Qualifikationen

  • Experience leading GMP analytical laboratories and people managers
  • Deep understanding of AQbD, validation, and lifecycle management
  • Experience across multiple analytical modalities (small molecules, biologics, vaccines, plasma-derived therapies)
  • Ability to drive technology adoption, automation, and data integrity in regulated labs

Aufgaben

  • Oversee operations, performance, compliance, and resourcing of US central and Japan regional analytical labs
  • Lead a multi-manager lab organization and build capability and high-performance culture
  • Collaborate with QA/QC, Regulatory, IT, and Manufacturing to align priorities and resources
  • Ensure GMP method performance, data integrity, and inspection readiness
  • Drive development, transfer, and troubleshooting of analytical methods across platforms

Kenntnisse

Leadership
Stakeholder management
Communication
AQbD
Digital analytics

Ausbildung

BS/MS in Analytical Chemistry / Biochemistry / Biology / Microbiology
PhD preferred

Tools

CDS
LIMS
ELN

Jobbeschreibung

Takeda seeks an accomplished pharma analytics leader to head its US central laboratory (Lexington, MA) and a Japan vaccines testing lab. You will steward GMP method performance, data integrity, and resource planning across modalities, ensuring strategic priority alignment with portfolio and quality standards.

The role requires 20+ years in pharma/biotech analytical development or QC, strong people leadership, and a track record of deploying new analytical tech, automation, and advanced analytics

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