Manager, Global Trade Compliance

2 weeks ago


Cambridge, Massachusetts, United States Takeda Full time $111,000 - $175,670 per year

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 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 Compliance based remotely 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:
Cambridge, MA

U.S. Base Salary Range :
$111, $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-term incentives. 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:
Cambridge, 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.



  • Cambridge, Massachusetts, United States RTX Full time $137,000 - $275,000

    Date Posted: Country:United States of AmericaLocation:MA105: BBN Headquarters 10 Moulton Street , Cambridge, MA, 02138 USAPosition Role Type:HybridU.S. Citizen, U.S. Person, or Immigration Status Requirements: The ability to obtain and maintain a U.S. government issued security clearance is required.​ U.S. citizenship is required, as only U.S. citizens...


  • Cambridge, Massachusetts, United States Jobs via Dice Full time

    Dice is the leading career destination for tech experts at every stage of their careers. Our client, Radiant System, Inc, is seeking the following. Apply via Dice todaySummary:The Global Category Manager (GCM) plans and leads complex global category initiatives for Real Estate & Capital Projects, primarily focused on office and lab space, with a typical...


  • Cambridge, Massachusetts, United States Boston Technology Corp Full time

    Subject Matter Expert (SME) on the Clinical Quality Compliance activities including deviation management, quality investigation, corrective and preventive actions (CAPA) management and oversight and change control. Represent Clinical Quality Compliance in these topics in inspections.Engages with relevant functions and stakeholders to ensure inspection...


  • Cambridge, Massachusetts, United States Infotree Global Solutions Full time $120,000 - $180,000 per year

    Client is preparing to launch product globally. We are looking for a contractor to:Work with the psoriasis GCL and his team to develop and monitor an integrated global launch plan that aligns with our asset and brand strategies.Facilitate cross-functional engagement with stakeholders across Clinical Development, Global Regulatory Affairs, Global...


  • Cambridge, Massachusetts, United States IPSEN Full time

    The Ipsen Global Partnering department includes the Business Development and Strategic Alliances Group activities. The department mission is to strengthen Ipsen products pipeline, by identifying, engaging, and leading key partnerships and alliances with other pharmaceutical/biotech companies to drive innovation and fuel Ipsen growth in Oncology, Rare Disease...


  • Cambridge, Massachusetts, United States Randstad Life Sciences US Full time

    Job SummaryClinical Quality Compliance LeadCambridge, MA (2 days per week onsite)12 Month Contract | w2 onlyTheClinical Quality Compliance Leadprovides critical quality oversight to clinical trial delivery systems, ensuring operational and compliance excellence across the organization. This role maintains a state of control by implementing effective...


  • Cambridge, Massachusetts, United States RSA Tech Full time

    Job Title: GCP Quality Compliance LeadLocation: Cambridge, MA (onsite 2 days/week)Experience: 10+ YearsInterview Mode: VirtualJob Description:Must Have:· Strong experience holding the responsibility and relevant experience in the global pharmaceutical industry in functions such as Clinical Operations, Data Management and Statistics, with at least 3 years of...


  • Cambridge, Massachusetts, United States RSA Tech Group Full time

    Role: GCP Quality ComplianceLocation: Cambridge, MA (onsite 2 days/week)Must Have:* Strong experience holding the responsibility and relevant experience in the global pharmaceutical industry in functions such as Clinical Operations, Data Management and Statistics, with at least 3 years of experience in GCP Quality/Compliance.* Advanced knowledge of...


  • Cambridge, Massachusetts, United States Biogen Full time

    About This RoleWe are seeking a strategic and execution-oriented leader to serve as the Global Access Mechanisms (GAM), Strategy & Governance Lead within the Worldwide Medical organization. This role will be instrumental in shaping and operationalizing Biogen's global access strategy through the development of a Center of Excellence (CoE) focused on...


  • Cambridge, Massachusetts, United States Biogen Full time $200,000 - $250,000 per year

    About This RoleWe are seeking a strategic and execution-oriented leader to serve as the Global Access Mechanisms (GAM), Strategy & Governance Lead within the Worldwide Medical organization. This role will be instrumental in shaping and operationalizing Biogen's global access strategy through the development of a Center of Excellence (CoE) focused on...