Manager, Global Trade Compliance
Location: Boston
Posted on: June 23, 2025
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Job Description:
By clicking the “Apply” button, I understand that my employment
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with Takeda’s Privacy Notice and Terms of Use . I further attest
that all information I submit in my employment application is true
to the best of my knowledge. Job Description Are you looking for a
patient-focused, innovation-driven company to inspire you and
empower you to shine? Join us as a Manager, Global Trade
Compliancebased in Cambridge/Lexington, MA reporting to the Senior
Director – Global Clinical Supply Chain Import Export Operations
and Global Trade Compliance. At Takeda, we are transforming the
pharmaceutical industry through our R&D-driven market
leadership and being a values-led company. To do this, we empower
our people to work towards their potential through life-changing
work. Certified as a Global Top Employer, we offer stimulating
careers, and work toward excellence in everything we do. We foster
an inclusive, collaborative workplace, in which our global teams
are united by an unwavering commitment to provide Better Health and
a Brighter Future to people around the world. Here, you will be a
necessary contributor to our inspiring, bold mission. GOALS: The
Global Trade Compliance Manager will ensure that Clinical and
R&D imports and exports are conducted in accordance with the
rules and regulatory requirements of Customs and other applicable
governmental agencies in the affected countries. The position
emphasizes developing opportunities for process improvements while
working with colleagues at all global locations on import/export
compliance activities and recommending/implementing solutions
leading to such improvements. A CCOUNTABILITIES: Contribute to the
creation and adherence of export and import compliance policies and
procedures for the organization regarding Clinical Trial Material
(CTM) and raw material shipments. Manage daily import and export
transactions ensuring compliance to all US Government Laws and
Regulations. This includes US Customs and Border Protection, USDA,
FDA, Fish Wildlife, Public Health, Bureau of Industry and Security,
DEA, FAA and possible other government agencies. This includes
generating shipping documentation, working closely with the
requester on specific to imports or exports. Ensure adherence to
country specific standard operating procedures for
importing/exporting clinical trial material and raw materials,
including logistics, customs clearance and delivery cycle times.
Liaise with in-country coordinators/CRO’s to establish and maintain
standard import and export requirements for clinical trials,
including export license determination. Help to maintain all
international product data for development compounds: Country of
Origin, Harmonized Tariff Codes, Export Commerce Control Number
(ECCN), PGA Licenses & Permits, FDA product codes, INDs for raw
materials, chemical intermediates, and finished goods. Instruct
customs brokers and freight forwarders on how to handle the
import/export transaction. Conduct post-entry review ensuring
transactions comply with US import regulations. Provide guidance
and valuation for non-commercial materials using WCO/WTO
recommended best practices. Have proven experience identifying,
forecasting and mitigating import VAT costs across multiple tax
regimes. Identify key opportunities for process improvements and
implement solutions to eliminate identified compliance
deficiencies. Work closely with global colleagues in Clinical
Supply Chain Operations and Legal to assure alignment of import and
export compliance related activities within Takeda. Verify all
international product data for CLINICAL AND RESEARCH AND
DEVELOPMENT SUPPLIES: Country of Origin, Tariff Code/Schedule B,
Export Commerce Control Number (ECCN), FDA product codes, NDAs,
INDs for raw materials, chemical intermediates, and finished goods,
are the ones determined and established by the Trade Compliance
group. EDUCATION AND EXPERIENCE: Bachelor’s degree, preferred in
Business or Science. US Customs Broker Licensed required.
Experience with South American customs required. 6 or more years
experience in importing and exporting in a technical industry
involving chemicals and controlled materials. Expert knowledge of
the Export Administration Regulations (EAR) required. Knowledge and
Ability to interpret EU, US and MERKOSUR Customs regulations and
apply to Takeda businesses required. Solid understanding of US
Automated Export System via ACE required. Export auditing
experience preferred. Bonded Warehousing and Free Trade Zone
experience preferred. Well-developed supply chain knowledge
preferred. Excellent communication, organizational, interpersonal,
and writing skills and personal judgment. Ability to work
independently and exercise independent sound judgment. Ability to
clearly advise, explain and discuss material and complex matters
with internal colleagues and external customers. Ability to
develop, present, and follow through on innovative solutions. Must
be a team player; ability to develop and utilize collaborative
relationships. Leadership skills – ability to lead and train
cross-functional project teams. Takeda Compensation and Benefits
Summary We 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, MA U.S.
Base Salary Range: $111,800.00 - $175,670.00 The 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 Statement Takeda 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. Locations Boston, MA Worker Type
Employee Worker Sub-Type Regular Time Type Full time Job Exempt Yes
It 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.
Keywords: , Attleboro , Manager, Global Trade Compliance, Science, Research & Development , Boston, Massachusetts