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Counsel, Global Supply Chain, Trade, and Human Rights
Bristol Myers Squibb
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About this role
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.
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. Read more: careers.bms.com/working-with-us .
Position Summary The Counsel, Supply Chain, Trade, and Human Rights serves as a legal advisor to the Global Supply Chain (GSC) organization, including its Customs & Trade function. This attorney provides strategic, regulatory, and transactional counsel across the clinical and commercial supply networks that deliver BMS medicines to patients around the world. This is a high-visibility role focused on issues including tariffs, trade policy, sanctions, import/export controls, supply continuity, and human rights due diligence. This attorney will collaborate closely with others in Law & Policy and the business. The role sits within the Product Development & Supply (PDS) Law team, a collaborative and dynamic group within the Global Drug Development, Manufacturing & Corporate Transactions (GDMCT) legal team at BMS. The PDS Law team provides comprehensive legal support for internal and external manufacturing operations, supply chain, customs and trade, engineering, real estate, and EOHSS. The broader GDMCT legal team also supports Drug Development, Product Development, Global Quality, and transactional support across the enterprise. This attorney will work alongside colleagues with deep subject matter expertise across manufacturing, quality, regulatory, and transactional practices, on work that is directly connected to the delivery of medicines to patients. The successful candidate brings excellent legal judgment, learns quickly, navigates complexity, and works with urgency and creativity across regulatory schemes and stakeholders, always prioritizing the urgent needs of patients. The ability to build programs and communicate clearly on complex topics with senior business stakeholders is critical to success in this role. Responsibilities • Serve as a legal advisor to the Global Supply Chain organization, advising on complex issues that arise in the supply of product across the clinical and commercial networks to enable the urgent delivery of medicines to patients.
• Serve as a legal advisor on global trade matters, including tariffs and trade remedies, customs and import/export compliance, economic sanctions, export controls, and trade-related licensing, working closely with Customs & Trade leads to develop practical mitigation and compliance strategies.
• Serve as a legal advisor on human rights matters, including due diligence related to forced labor, responsible sourcing, supply chain transparency, and emerging human rights laws and standards, partnering with business and compliance stakeholders to assess risk and develop practical mitigation strategies.
• Monitor evolving global trade and supply chain regulations and enforcement trends, and proactively advise senior leadership on business impact, risk mitigation, and opportunities.
• Draft, review, and negotiate complex supply, logistics, transportation, and warehousing agreements.
• Advise on supply disruption, business continuity, and crisis response matters affecting the global network.
• Collaborate across the Law & Policy Department, including regulatory, ESG, policy, litigation, and IP colleagues, to deliver coordinated, enterprise-aligned legal support to GSC.
Required Qualification(s) and Desired Experience • JD (or equivalent) and admission in good standing to at least one U.S. state bar; qualified, or able to become qualified, to practice in-house in New Jersey.
• 6 or more years of legal experience across law firm, in-house, and/or government roles, including experience in the pharmaceutical or life sciences industry.
• Experience in human rights, customs, international trade, sanctions, or supply chain matters is preferred.
• Experience structuring and negotiating complex commercial transactions is preferred.
• Demonstrated ability to build strong relationships and to advise and influence senior executives, including SVP and C-suite stakeholders, on high-impact legal and regulatory matters.
• Proven ability to lead across large, global, matrixed organizations and to bring stakeholders together to resolve complex issues efficiently and improve the management of legal risk.
• Excellent judgment, with the ability to independently prioritize and manage multiple projects and to work with speed and quality on a broad range of matters.
• Ability to communicate complex issues clearly and concisely, verbally and in writing, to senior leaders.
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If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
Compensation Overview:
Madison - Giralda - NJ - US: $202,050 - $244,831
Princeton - NJ - US: $202,050 - $244,831 
 The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-r
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