Takeda Pharmaceutical jobs in Minnesota

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VALIDATION MAINTENANCE MANAGER - BOSTON, UNITED STATES - TAKEDA PHARMACEUTICAL

Assess, qualify and validate equipment, critical systems (utilities), facilities, computerized systems, cleaning and sterilization processes. Coordinate with manufacturing and production schedules to access equipment to perform re...

CompanyTakeda Pharmaceutical
AddressUnited States
CategoryManufacturing
Date Posted 3 days ago See detail

Validation Maintenance Manager - Boston, United States - Takeda Pharmaceutical

Takeda Pharmaceutical

United States

Assess, qualify and validate equipment, critical systems (utilities), facilities, computerized systems, cleaning and sterilization processes. Coordinate with manufacturing and production schedules to access equipment to perform re...

Head, Clinical Partner Management - Boston, United States - Takeda Pharmaceutical

Takeda Pharmaceutical

United States

Lead Clinical Partner Management group, which partners with Therapeutic Area Units, Clinical Operations, and Clinical Site Startup & Engagement to launch and deliver effective clinical programs by supporting outsourcing activities...

Scientist, Process Chemistry - Boston, United States - Takeda Pharmaceutical

Takeda Pharmaceutical

United States

Contribute to the preparation of technical reports, patent applications, and scientific publications to communicate research findings. Design and develop laboratory proof of concept for new, concise synthetic routes to challengin...

R&D Digital Health Product Manager

Takeda Pharmaceutical

New York, United States

Own enhancements to asset strategy by supporting Global Project Teams (GPTs) with design and execution of highest value Digital Health Products (DHPs), considering operational and commercial aspects as well as the longer strategic...

Senior Director, GRA Pharmaceuticals - Boston, United States - Takeda Pharmaceutical

Takeda Pharmaceutical

United States

Leads the Early Development Pharmaceuticals GRA CMC regulatory team in the development and implementation of global CMC regulatory strategies during development ,commercialization and post approval LCM stages. Combines knowledge o...

Manufacturing Lead Investigator - Boston, United States - Takeda Pharmaceutical

Takeda Pharmaceutical

United States

Conduct investigations of moderate scope and complexity where analysis of situations or data requires a review of a variety of factors to determine product impact, identify cause, and identify corrective and preventative actions....

Senior Director, GRA Pharmaceuticals - Newark, United States - Takeda Pharmaceutical

Takeda Pharmaceutical

United States

Leads the Early Development Pharmaceuticals GRA CMC regulatory team in the development and implementation of global CMC regulatory strategies during development ,commercialization and post approval LCM stages. Combines knowledge o...

Senior Director, GRA Pharmaceuticals - Philadelphia, United States - Takeda Pharmaceutical

Takeda Pharmaceutical

United States

Leads the Early Development Pharmaceuticals GRA CMC regulatory team in the development and implementation of global CMC regulatory strategies during development ,commercialization and post approval LCM stages. Combines knowledge o...

Scientist - Boston, United States - Takeda Pharmaceutical

Takeda Pharmaceutical

United States

I further attest that all information I submit in my employment application is true to the best of my knowledge.Takeda Development Center Americas, Inc. is seeking a Scientist in Cambridge, MA with the following requirements: Bach...

Senior Manager, Feasibility - Boston, United States - Takeda Pharmaceutical

Takeda Pharmaceutical

United States

Conduct data-driven feasibility assessments for Phase I IV clinical studies, including protocol design optimization, country/site feasibility and selection, enrollment strategy, and modeling. Use all competitive intelligence dat...

Manager, Feasibility - Boston, United States - Takeda Pharmaceutical

Takeda Pharmaceutical

United States

Conduct data-driven feasibility assessments for Phase I IV clinical studies, including protocol design optimization, country/site feasibility and selection, enrollment strategy and modeling, with limited supervision. Utilize int...