What are the responsibilities and job description for the Associate Director, Program Management, Global Operations position at Bristol-Myers Squibb?
Job Description
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment.
About Us
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.
Job Summary
Associate Director, Program Management, Global Operations (Inline Asset Program Management)
About the Role
The Associate Director, Program Management plays an important role in organizing, managing, and communicating the portfolio of projects aligned to the CTDO goals and objectives for specific asset/s, as well as providing project management skills and leadership for Inline products.
Key Responsibilities
- Lead planning and execution of integrated, complex plans and teams for strategic CTO team programs & projects, tech transfer governance, or GO team program management and other critical initiatives as defined by CTD/O management.
- Leads GO team operations including recurring status meetings, reporting, risk tracking, steering committee meetings, and conflict resolution.
- Develop and own execution plan for pre-launch, launch and post-launch activities aligned with asset/s strategy in partnership with the Product leader.
- Coordinate across GO sub-teams to align, organize and provide direction aligned with strategy.
- Prepare and manage governances until final decision and implementation.
- Leads and guides BOW for asset/s across CTDO based on prioritization for respective GO team/s.
- E2E operational management including budget, forecasting, performance against targets, facilitate key investment decision preparation / discussions in partnership with the Program leader.
Requirements
- B.S. in Engineering, Pharmacy, science or technical discipline, advanced degree preferred.
- PMP certification highly desirable.
- Understanding of cGMPs and regulatory CMC.
- A minimum of 10 years in BioPharma operational or development discipline, including demonstrated experience managing complex projects.
- Experience in project/program management of complex projects involving cross-functional, multi-site, international teams.
- Experience with manufacturing sites and staff.
- Proficiency with project management and Microsoft tools e.g. Project, Excel, PowerPoint, SharePoint.
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.
Please visit our careers site for more information on benefits.
