Commercial Supply Planning Manager, CSO

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 rich in diversity. 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: .

Our Clinical Supply Operations is responsible for the supply of drug product administered to patients in clinical studies worldwide. In Global Product Development and Supply the team works closely with our partners to deliver quality products safely, efficiently and on time while operationalizing the innovative technologies that will deliver the transformative medicines of tomorrow. As a member of our team, you will get the chance to play a pivotal role to positively impact patients' lives while developing professionally to achieve your own career goals.

Role & Responsibilities: Supports central planning function in Clinical Supply Operations (CSO) R&D supply chain. The incumbent is responsible, on a monthly cycle, for maintaining and updating the pharma commercial sourced dosage form drug product supply plans based on current clinical and development demand and on obtaining an endorsed supply plan (as expressed as a rough cut schedule) by respective responsible operating departments.Participates in Bio and Pharma cycle S&OP and as key DP demand representative in Bio and Pharma Commercial Network, including interaction with SCPL (Supply Chain Product Lead), NSP (Network Supply Planning), Site Supply Chain (primarily Boudry), and Long-term Supply Planning.Creates, reviews and monitors long and short range Bio and Pharma commercial sourced dosage form demand and proposes supply scenarios, along with SKU setup/config to enable interfaces (clinical to commercial; planning propagation to production and delivery); oversight of Commercial DP for clinical through to P&L site receipt.Collaborates with CSO Clinical Supply Services group, CSO Functional Teams and Site Operations (primarily Manati, Boudry and any other network nodes as adjusted) to facilitate decision making by providing information such as schedule challenges/ disruptions on a 36 month outlook monthly update, as well as LTFP of clinical demand for Pharma productsManages on-boarding readiness meetings for any new formulations moved to Bio and Pharma Commercial Network where key deliverables by CMC development are reviewed to enable production against projected timelinesCoordinate Commercial API for clinical DP oversightAct as strategic voice to on-board the planning and execution tasks via creation and maintenance of project plan and communication aids. This model may involve elements such as: multiple cross functional hand-offs that are time sensitive; multiple hand-offs with external supply chain partners; multiple geographies with a mix of inhouse and external partners.Experience & Qualifications:BS in Pharmacy/Chemistry, Industrial/Chemical Engineering, Business or related focus.Master's degree or MBA with a Supply Chain focus is a plus.3+ years' experience in Supply Chain, Production Planning, Business Operations or a related environment. Must demonstrate a high level of performance in these areas.Knowledge of SAP planning transactions.Basic understanding of solid dosage form processes.Must be an effective communicator with the ability to collaborate across multiple levels in the organization. Must be good at follow up and ensure that timelines are met.Must have good leadership skills and the ability to lead projects/tasks.APICS education/certifications a plus. Why You Should Apply

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 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 . Visit to access our complete Equal Employment Opportunity statement.

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.

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 an inclusive culture, promoting diversity 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 a diverse 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.

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 eeo -accessibility to access our complete Equal Employment Opportunity statement.

BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.

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

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

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