Celgene

Senior Manager, North America Import/Export Customs & Trade Compliance

Posted on: 22 Mar 2021

New Brunswick, NJ

Job Description

At Bristol Myers Squibb, we are inspired by a single vision transforming patients lives through science. In oncology, hematology, immunology and cardiovascular disease and one of the most diverse and promising pipelines in the industry each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.

Job Summary

* Support the strategy for managing Import and FTZ compliance in the North America Region.
* Support the development of directives, procedures and processes for managing Import and FTZ compliance
* Provide guidance and direction for HTS assignments and Customs Clearance Instructions
* Provide guidance and direction to SIAs and FTZAs on Customs Compliance matters
* Develop and deliver training as needed.
* Evaluate, implement, and support opportunities for optimizing duty savings associated with Customs imports by conducting duty analyses and use of duty minimization programs (i.e., FTZs and FTAs), prototype provision and establishing processes for compliance
* Facilitate and oversee site self-assessment programs
* Provide assistance in preparation for Import /FTZ and other Customs Compliance related audits and directly support audits
* Work with sites to determine business changes required to address new regulations or changes to regulations
* Collaborate with internal functions including, but not limited to, Global Quality, Product Security, Legal, Shipping and Receiving, Import/Export, IT, Site Security, etc. for trade compliance-related activities and initiatives. Build strong partnership with peer groups and departments.
* Stay abreast of new, amended, or proposed regulatory activities to determine impact to operations and business objectives, implement necessary program modifications, and effectively communicate throughout the organization

Competencies

* Strong knowledge of BMS business practices and philosophies.
* Demonstrated ability to interpret Government Regulations and transfer complex regulations to existing business processes.
* Demonstrated ability to effectively communicate ideas, lead and persuade others to accomplish challenging goals and objectives.
* Demonstrated project management and team building skills.
* Demonstrated ability to analyze and interpret complex problems/data gathered from a variety of sources and, through effective decision-making and planning, and deliver superior business solutions.
* Demonstrated ability to lead a diverse team in a high performance culture and complex changing environment to deliver results which contribute to BMS performance, sustainability and growth.
* Demonstrated ability to influence, collaborate and communicate directly and to lead cross functional and cross regional teams

Qualifications

* Bachelors degree in Business, Finance, Engineering or related areas preferred. MBA degree a plus
* Minimum 5 years experience in direct management function. Minimum 10 years experience in BMS Manufacturing, Supply Chain, Finance or Logistics preferred.
* Knowledge of Customs regulations and FTZ management principles.
* Knowledge of FDA regulations as they apply to imports.
* Knowledge Export Controls, Sanctions, Anti-boycott and Restricted Party Screening regulations.
* Knowledge of import/export practices for Americas regions.
* Understanding of global biologics manufacturing, logistics and distribution operations.
* Strong computer skills. Experienced in Excel, Word, PowerPoint, and SAP.
* Licensed U.S. Customs Broker and/or NCBFAA Certified Customs Specialist (CCS) preferred.

Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.

Our company is committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an approval of accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application, or any part of the recruitment process direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Celgene

Summit, NJ

Celgene Corporation, a biopharmaceutical company, discovers, develops, and commercializes therapies for the treatment of cancer and inflammatory diseases worldwide. It offers REVLIMID, an oral immunomodulatory drug for multiple myeloma (MM), myelodysplastic syndromes (MDS), and mantle cell lymphoma; POMALYST/IMNOVID to treat multiple myeloma; OTEZLA, a small-molecule inhibitor of phosphodiesterase 4 for psoriatic arthritis and psoriasis; and ABRAXANE to treat breast, non-small cell lung, pancreatic, and gastric cancers.

The company’s products also include IDHIFA for the treatment of adult patients with relapsed or refractory acute myeloid leukemia (rrAML) with an isocitrate dehydrogenase-2 mutation; VIDAZA, a pyrimidine nucleoside analog for intermediate-2 and high-risk MDS, chronic myelomonocytic leukemia, and AML; THALOMID to treat patients with MM; and ISTODAX, an epigenetic modifier. Its preclinical and clinical-stage product candidates include small molecules, biologics, and cell therapies for immune-inflammatory diseases, myeloid diseases, epigenetics, protein homeostasis, and immuno-oncology.

The company has agreements with BeiGene, Ltd; Acceleron Pharma, Inc.; Agios Pharmaceuticals, Inc.; bluebird bio, Inc.; Lycera Corp.; Juno Therapeutics, Inc.; EXSCIENTIA LTD.; and IMIDomics SL, as well as immuno-oncology collaboration with Sutro Biopharma. Celgene Corporation was founded in 1980 and is headquartered in Summit, New Jersey.

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