External Partner Manager

Working with Us
Challenging. Meaningful. Life-changing. Those arent 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. Youll 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: science doesnt stop at our walls.

Youve spent years in the lab in manufacturing suites in development teams - understanding what it really takes to turn a molecule into a medicine. You know the complexity the precision and the stakes involved.

Now imagine taking that expertise and using it to shapehowBMS works with the worlds leading external partners to get life-changing therapies to patients faster.

Thats exactly what this role is about.

So what will you actually be doing

Think of yourself as the bridge between BMS Product Development and the external manufacturing ecosystem. Youll be thesingle point of contactfor our Strategic Sourcing & Procurement teams and the go-to person for managing relationships with CDMOs (Contract Development and Manufacturing Organisations) who handle drug substance and drug product manufacturing on our behalf.

In practice that means:

• Youll be in the room where decisions get made.Sitting on joint steering committees alongside senior leaders from BMS and our external partners youll be driving the conversations that shape outcomes for our pipeline - not just reporting on them.
• Youll protect the programme not just the paperwork.By leading Virtual Development Operation Teams (VDOTs) youll hold external partners accountable for performance - ensuring timelines quality and commitments are met for real assets that real patients are waiting on.
• Youll build strategies that future-proof our pipeline.Working alongside colleagues across PD Quality and Legal youll help develop sourcing strategies that dont just fill capacity gaps today - they bring in genuine innovation bridge technology gaps and set us up for tomorrow.
• Your technical background will directly translate into commercial impact.Youll be the one turning complex development requirements into Statements of Work Master Service Agreements and Request for Proposals - meaning your scientific fluency becomes acompetitive advantageat the negotiating table.
• Youll own the full partner lifecycle.From first qualification through to decommissioning youll steer vendor onboarding with Global Quality and GOEHSS - ensuring every external partner is set up for success from day one.

Whats in it for you

Lets be honest this isnt just a step up. Its astep outinto a part of drug development that most scientists never get visibility into but which underpins everything.

• Broaden your career horizon.Your scientific background becomes the foundation for a role that spans strategy commercial negotiation and operational leadership. Few roles offer this kind of cross-functional breadth.
• See your work matter - at scale.The partnerships you manage directly support a portfolio of BMS assets moving through development and into manufacturing. The decisions you make have a direct line to patient impact.
• Build your leadership identity.Leading matrix teams influencing without authority and representing BMS in senior-level governance forums - this is the environment where people become the kind of leader others want to follow.
• Gain commercial fluency without leaving science behind.Youll negotiate terms shape agreements and develop sourcing strategies - all grounded in a scientific understanding that gives you instant credibility with internal and external stakeholders alike.
• Work at the frontier of external innovation.BMSs external partner network isnt just a capacity safety net - its a source of cutting-edge technology and capability. Youll have a front-row seat to whats emerging across the CDMO landscape.

Is this you

You likely have a degree in chemistry pharmaceutical science engineering or a related discipline (BS MS or PhD) andat least five years of hands-on experiencein small molecule drug substance and drug product development clinical or commercial manufacturing.

But beyond the CV youre someone who:

• Naturally builds trust - with colleagues partners and leadership
• Can hold a technical conversation with a formulation scientistanda legal team in the same afternoon
• Is comfortable leading teams who dont directly report to you
• Knows that the best outcomes come from collaboration not command

If youve ever found yourself thinkingI want to understand how the bigger picture fits together- this role was built for people like you.

Ready to shape what comes next

At BMS were driven by a single mission - to discover develop and deliver innovative medicines that help patients prevail over serious diseases. The partnerships youll manage in this role are a critical part of making that happen.

Come and be the person who makes them work.

#LI-Hybrid

If you come across a role that intrigues you but doesnt 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.

Uniquely Interesting Work Life-changing Careers
With a single vision as inspiring as Transforming patients lives through science every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture promoting global participation in clinical trials while our shared values of passion innovation urgency accountability inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential site-by-design field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles onsite presence is considered an essential job function and is critical to collaboration innovation productivity and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

Supporting People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application or in any part of the recruitment process direct your inquiries to . Visit to access our complete Equal Employment Opportunity statement.

Bristol Myers Squibb is Disability Confident Employer

A UK Government scheme

Candidate Rights

BMS will consider for employment qualified applicants with arrest and conviction records pursuant to applicable laws in your area.

Data Protection

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