Job Description

At Bristol Myers Squibb, we are inspired by a single vision transforming patients lives through science. In oncology, hematology, immunology and cardiovascular disease and one of the most diverse and promising pipelines in the industry each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.

PURPOSE AND SCOPE OF POSITION:

This role is accountable to manage a well-designed and integrated supply plan from controlled-non-classified (CNC) material receipt to manufacturing delivery.

DUTIES AND RESPONSIBILITIES:

Responsibilities will include, but are not limited to the following:

People Leadership

* Develop and manage team member resource allocation & shift schedules to meet workflow demands
* Coach and counsel team members to develop their skill sets and create an environment of continuous learning, teamwork, transparency and a sense of urgency
* Communicate with stakeholders inside and outside of Supply Chain to drive successful outcomes for the site and functional business unit
* Maintain and communicate performance metrics for team, setting and maintaining high expectations for team performance & compliance with BMS Values

Material Receiving & Warehousing

* Manage raw material/consumable receipt, labeling & storage, expediting activities when required by stakeholders
* Maintain & control bin locations in the Warehouse & QC labs
* Manage receipt of patient material and patient process intermediates
* Conduct investigations and root cause analyses on any supply disruptions or material quality issues; report on corrective actions
* Identify strategic and operational issues both internally and externally, develop proposals, outline solutions, and provide time commitments and resources
* Coordinate, manage and perform regular physical inventory counts as scheduled

Safety & Quality

* Ensure a safe work environment is maintained in all areas where group activities occur
* Promote and engage team in safety and safety training program; foster a culture of compliance and strong environmental, health, and safety performance
* Assure compliance with all FDA, DEA, DOT, ISBT, CTPAT, OSHA, VAWD, cGMPs and applicable policies
* Manage the creation, implementation and maintenance of documentation, procedures and training curricula
* Own and manage change controls, deviations and corrective/preventive actions
* Ensure appropriate training and qualification for staff activities performed

Operational Excellence

* Participate in and/or lead cross-functional teams to improve systems, processes or internal/external performance
* Perform other duties as assigned
* Limited global travel up to 10% of time may be required

REQUIRED COMPETENCIES: Knowledge, Skills, and Abilities:

Education:

* Bachelors degree required in Life Sciences, Engineering, Supply Chain, or similar
* 5+ years relevant work experience required (preferably in GMP biologics manufacturing or process support
* 3+ years of experience in warehousing, manufacturing and supply chain areas
* An equivalent combination of education, experience and training may substitute.
* Preferred but not required: Certification in CPIM, CSCP, and/or CLTD

Experience:

* Advanced proficiency in ERP systems and analytics tools
* Advanced knowledge of fundamental concepts of materials management, planning and site production scheduling
* Ability to effectively communicate problem statements and viable solution options using pro vs. con and cost vs. benefit approaches
* Ability to present data and analyses in an organized, clear and concise manner
* Advanced proficiency in MS Office applications
* Excellent written and verbal communication skills
* People management experience
* Experience in biopharmaceutical clinical, supply chain, manufacturing, and commercialization
* Experience with lean six sigma projects and change execution management
* Ability to work independently for extended periods of time
* Ability to work as a team and mentor peers and direct reports
* Ability to understand and solve complicated problems
* Intermediate knowledge of cGMP/Pharmaceutical regulations

BMSCART

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.