Director, Life Cycle Assessment & Product Stewardship

At Bristol Myers Squibb our employees often ask Who are you working fora 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.

This is an exciting opportunity to join a growing and passionate team that is focused on being a world class Product Stewardship group within Bristol Myers Squibbs Environment Health Safety and Sustainability Enablement organization. As a member of the Product Stewardship group the successful applicant will be primarily responsible for the technical execution of Product Carbon Footprints (PCFs) /Life Cycle Assessment (LCAs) as well as development of the PCF/LCA multi-year strategy advising where the company invests development of digital PCF/LCA tools how PCF LCA is embedded into product development and procurement decisions and how we engage suppliers and external standards bodies. The successful candidate will be the internal authority on product environmental footprinting and the person who turns it from a set of one-off studies into a scalable decision-grade addition to working on PCFs/LCAs the successful applicant will have the opportunity to help operationalize other Product Stewardship regulations across the business. Additionally they will have the opportunity to participate in other aspects of the Product Stewardship program (e.g. global research projects environmental support of sites extended producer responsibility chemical registrations hazard communication) as time permits. This role will also act as a primary back up for the Product Stewardship Lead.

Key Responsibilities:

• Serve as BMSs subject-matter expert and strategic lead for LCAs and PCFs
• Build run and critically review cradle-to-gate and cradle-to-grave LCAs/PCFs for BMS Products that are audit-ready and third-party-verifiable.
• Build the internal operating model: governance standard methodologies digital tools data-management systems and the tools and training that let non-specialists across the company use PCF/LCA outputs
• Own PCF/LCA technology implementation and lifecycle including guiding the maturing Watershed platform on tool design data quality and fit to evolving business and regulatory needs
• Translate external product-stewardship regulations/mandates into executable internal programs and repeatable workflows
• Represent BMS in industry workstreams/projects
• Work with the Environment and Sustainability Enablement (ESE) group to embed life cycle thinking into design formulation packaging device and sourcing decisions early enough to change outcomes and build a roadmap for how LCA/PCF informs development.

Qualifications & Experience:

• Advanced degree (M.S. or Ph.D. preferred) in environmental engineering chemical engineering industrial ecology chemistry or a related field or a bachelors degree with equivalent demonstrated LCA/PCF experience
• 10 years of relevant industrial experience including demonstrated hands-on delivery of cradle-to-grave life cycle assessments and product carbon footprints; pharmaceutical biotech or life sciences industry experience is a plus; Engagement with pharma-sector harmonization efforts is a plus.
• Working fluency in the governing standards: ISO 14040/14044 (LCA) ISO 14067 (product carbon footprint) and the GHG Protocol Product Standard with familiarity with the pharma-specific PAS 2090:2025 product category rules and the French medicine carbon score methodology.
• Hands-on proficiency with recognized LCA software (e.g. SimaPro GaBi) and life cycle inventory databases (e.g. ecoinvent). Familiarity with Watershed is a plus.
• Demonstrated ability to produce robust low-uncertainty third-party-verifiable PCFs/LCAs including managing data quality boundary setting and uncertainty analysis to a standard that survives independent verification and audit.
• Experience operationalizing product-stewardship or environmental regulations in a regulated industry translating an external requirement into an executable internal program
• Ability to translate technical results into clear business regulatory and commercial decisions for non-technical stakeholders including senior leadership
• Ability to innovate and encourage others to do so as well. Strives to enhance performance by doing things that are unique and leading edge; experience with AI and/or automation is a plus
• Strong cross-functional collaboration across procurement manufacturing regulatory commercial and sustainability/disclosure functions
• Willingly embraces changes needed to adapt to new circumstances and uncertainties

#LI-Hybrid

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

Compensation Overview:

Devens - MA - US: $197230 - $239001 New Brunswick - NJ - US: $179300 - $217268

The starting pay range(s) listed above is for full-time employees (FTE). You may also be eligible for additional discretionary incentive cash and stock opportunities. We determine starting pay thoughtfully carefully considering the nature of the role required skills work location schedule and the knowledge and experience you bring. Final compensation is guided by pay equity principles and applicable employment laws. Compensation programs are reviewed on an ongoing basis and may be adjusted over time to reflect evolving market factors and individual team or Company performance.

Benefits:

Subject to the terms and conditions of the applicable plans then in effect you may be eligible to participate in our comprehensive benefit plans including wellbeing support retirement and financial protection benefits and insurance offerings (medical dental vision life and disability).

U.S.-based exempt employees are eligible for Flexible Time Off (FTO) which provides paid time off without a set accrual limit subject to manager approval along with 11 paid company holidays each year.

Non-exempt employees RayzeBio employees and employees located in Puerto Rico receive 160 hours of paid vacation annually for new hires (subject to manager approval) 11 paid company holidays and 3 optional holidays.

Depending on eligibility employees may also have access to additional time-off benefits including paid sick leave up to two paid volunteer days per year summer hours flexibility and leaves of absence for medical personal parental caregiver bereavement or military needs. Eligible employees also enjoy an annual Global Shutdown between Christmas Day and New Years Day.

U.S.-based job seekers can explore full benefit offerings at We Work

Where you work matters because collaboration innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential site-by-design field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at People with Disabilities

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