Bristol Myers Squibb logo
Bristol Myers Squibb · Life sciences

Senior Counsel, Supply Chain, Trade, and Human Rights

Bristol Myers Squibb Princeton, NJ Posted Sep 16, 2026
Location
Princeton, NJ
Workplace
On-site / per employer
Posted
Sep 16, 2026

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits.

This is work that transforms the lives of patients, and the careers of those who do it.

The Senior 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, product

development, supply chain, human rights, customs and trade,

engineering, real estate, and EOHSS. The broader GDMCT legal

team also supports Drug 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.

Qualifications

  • 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.

  • 8 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.

#LI-Hybrid

We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway.

Compensation Overview

Madison - Giralda - NJ - US: $221,340 - $268,212

Princeton - NJ - US: $221,340 - $268,212

Washington DC - US: $221,340 - $268,212

Originally posted by Bristol Myers Squibb. View original posting