Head of Central Analytical Lab & Tech Innovation

Takeda Pharmaceutical Co.

Lexington (MA)

On-site

USD 212,000 - 333,000

Full time

3 days ago
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Job summary

Takeda Pharmaceutical Co. in Lexington, MA seeks an accomplished laboratory leader to oversee the US central and Japan regional analytical labs, ensuring GMP method performance, data integrity, and inspection readiness.

This role drives cross-modality technical strategy, staffing, and collaboration with QA, Regulatory, and IT to enable advanced analytics and scalable lab operations. The ideal candidate will bring 20+ years of pharma/biotech leadership, AQbD experience, and a track record of

Qualifications

  • BS/MS in Analytical Chemistry, Biochemistry, Biology, Microbiology, or related field (PhD preferred).
  • 20+ years in pharma/biotech with depth in Analytical Development and/or QC, including leadership of GMP analytical laboratories.
  • Experience leading GMP analytical laboratories - method lifecycle, capacity, instrumentation, data integrity.
  • AQbD, risk-based validation/verification, robustness, and method lifecycle management.
  • Knowledge of analytical platforms across modalities and informatics systems (CDS/LIMS/ELN).

Responsibilities

  • Own operations, performance, compliance, and resourcing of US central and Japan regional laboratories.
  • Lead a multi-manager laboratory organization and build capability and succession.
  • Interface with stakeholders to align on prioritization, resources, and technology plans.
  • Drive GMP method validation, tech transfer, and lifecycle management.
  • Support regulatory submissions, inspections, and data integrity posture.

Skills

Analytical leadership
Multi-modality testing
AQbD risk-based thinking
GMP compliance
Regulatory submissions

Education

BS/MS in Analytical Chemistry or related

Tools

LIMS
ELN
Automation

Job description

Takeda Pharmaceutical Co. in Lexington, MA seeks an accomplished laboratory leader to oversee the US central and Japan regional analytical labs, ensuring GMP method performance, data integrity, and inspection readiness.

This role drives cross-modality technical strategy, staffing, and collaboration with QA, Regulatory, and IT to enable advanced analytics and scalable lab operations. The ideal candidate will bring 20+ years of pharma/biotech leadership, AQbD experience, and a track record of

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