Associate Director, Regulatory Affairs Vaccines CMC
Company: Initial Therapeutics, Inc.
Location: Boston
Posted on: May 7, 2025
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'sand . I further attest that all information I submit
in my employment application is true to the best of my
knowledge.Job DescriptionOBJECTIVE / PURPOSE
- Providesprogram leadership and develops CMC regulatory strategy
in support of global vaccine programs in various stages of
development
- Represents the vaccine regulatory affairs team on
cross-functional Takeda Vaccines teams to ensure that data are
identified, obtained and effectively presented for the registration
and maintenance of vaccine licenses world-wide
- Demonstrates leadership and comprehensive understanding of
global vaccines CMC regulations and guidelines by applying
interpersonal skills and expert regulatory CMC knowledge to
identify, communicate, address, and overcome challenges that arise
during vaccine product development and commercialization
- Successfullycommunicates and negotiates with international
Health Authoritiesasnecessary, directly and
indirectly.ACCOUNTABILITIES
- Leads planning, execution, and management of regulatory
submissions for assigned vaccines in various phases of clinical
development, global marketing applications, and post-approval life
cycle activities, as needed
- Member of technical development teams which require experienced
interpretation of applicable EMA/FDA/ICH/WHO/Global regulations to
ensure CMC compliance within the organization
- Leads regulatory compliance assessments with respect to filing
requirements for assigned vaccines and/or changes throughout
development and the commercial life cycle
- Defines CMC strategy and content (data and documentation)
requirements for regulatory submissions and compiles/reviews this
content for conformance with established requirements
- Supports CMC preparation activities for meetings with Health
Authorities on CMC related matters as needed. Interacts directly
with international Health Authorities, as required. Participates in
and/or leads agency meetings on CMC topics
- Ensures project team colleagues, line management, and key
stakeholders are apprised of risks that may impact regulatory
success, exercising sound judgementand communicating in a
professional and timelymanner
- Stays up to date withcurrent and evolvingregulatoryCMC
requirements, appliesthis knowledge to assigned projects, and
shares knowledge and experience with others to support
theirdevelopment.EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS
- BS/BA Degree in a scientific/engineering discipline required,
Advanced Degree preferred
- 6 + years Regulatory CMC experience (vaccines or biologics
experience required). Alternatively, 4+ years Regulatory CMC
experience combined with 2+ years relevant vaccines or biologics
experience (e.g. Pharmaceutical Development, Process Development,
Analytical Development, Production, Quality Assurance)
- Experienced liaison with product development teams; experience
on global product developmentprogramspreferred
- Sound understanding of scientific principles and regulatory CMC
requirements relevant to global vaccine development, registration,
and post-market support
- Proven ability toprovide strategic regulatory guidance to teams
and experience with managing MAA content and format
- Demonstrated leadership, problem-solving ability,
flexibilityand teamwork
- Experience with regulatory registration of biological drug
substances or drug products (including sterile parenteral dosage
forms) is required
- Proven capability to apply good judgement in elevating and
communicating actual or potential regulatory risks to teams and
line management
- Excellent written and oral communication skills required.Takeda
Compensation and Benefits SummaryWe understand compensation is an
important factor as you consider the next step in your career. We
are committed to equitable pay for all employees, and we strive to
be more transparent with our pay practices.For Location:Boston,
MAU.S. Base Salary Range:$149,100.00 - $234,300.00The estimated
salary range reflects an anticipated range for this position. The
actual base salary offered may depend on a variety of factors,
including the qualifications of the individual applicant for the
position, years of relevant experience, specific and unique skills,
level of education attained, certifications or other professional
licenses held, and the location in which the applicant lives and/or
from which they will be performing the job.The actual base salary
offered will be in accordance with state or local minimum wage
requirements for the job location.U.S. based employees may be
eligible for short-term and/or long-termincentives. U.S.based
employees may be eligible to participate in medical, dental, vision
insurance, a 401(k) plan and company match, short-term and
long-term disability coverage, basic life insurance, a tuition
reimbursement program, paid volunteer time off, company holidays,
and well-being benefits, among others. U.S.based employees are also
eligible to receive, per calendar year, up to 80 hours of sick
time, and new hires are eligible to accrue up to 120 hours of paid
vacation.EEO StatementTakeda is proud in its commitment to creating
a diverse workforce and providing equal employment opportunities to
all employees and applicants for employment without regard to race,
color, religion, sex, sexual orientation, gender identity, gender
expression, parental status, national origin, age, disability,
citizenship status, genetic information or characteristics, marital
status, status as a Vietnam era veteran, special disabled veteran,
or other protected veteran in accordance with applicable federal,
state and local laws, and any other characteristic protected by
law.LocationsBoston, MAWorker TypeEmployeeWorker
Sub-TypeRegularTime TypeFull timeJob ExemptYesIt is unlawful in
Massachusetts to require or administer a lie detector test as a
condition of employment or continued employment. An employer who
violates this law shall be subject to criminal penalties and civil
liability.
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Keywords: Initial Therapeutics, Inc., Arlington , Associate Director, Regulatory Affairs Vaccines CMC, Executive , Boston, Massachusetts
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