Manager, Global Regulatory Affairs CMC Submissions Management
Company: Takeda Pharmaceutical
Location: Lexington
Posted on: October 23, 2024
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Job Description:
By clicking the "Apply" button, I understand that my employment
application process with Takeda will commence and that the
information I provide in my application will be processed in line
with Takeda's and . I further attest that all information I submit
in my employment application is true to the best of my
knowledge.Job DescriptionTakeda Development Center Americas, Inc.
is seeking a Manager, Global Regulatory Affairs CMC Submissions
Management in Lexington, MA with the following requirements:
Bachelor's degree in a scientific field or foreign academic
equivalent plus 4 years of related experience. Required skills:
Ability to work with firm deadlines and adapt quickly to changing
requirements and priorities; develop/maintain strong working
relationships with the regulatory CMC team and cross-functional
teams, participate on and/or lead multifunctional teams, handle and
prioritize multiple projects and work independently; experience
with global CMC regulations for advanced therapies and biological
compounds; knowledge of worldwide CMC regulatory requirements and
successful track record of delivering dossiers that comply with
these, particularly for new medicines in development. Up to 20%
domestic travel required. Up to 50% remote work allowed.Full time.
$178,500 - $202,000 per year.Apply on-line at and search for Req
#R0133816.LocationsLexington, MAWorker TypeEmployeeWorker
Sub-TypeRegularTime TypeFull time
Keywords: Takeda Pharmaceutical, Quincy , Manager, Global Regulatory Affairs CMC Submissions Management, Executive , Lexington, Massachusetts
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