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SENIOR PROJECT MANAGER

Bristol-Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases.
One shared journey is moving us forward at Bristol-Myers Squibb.
Around the world, we are passionate about making an impact on the lives of patients with serious disease.
Empowered to apply our individual talents and ideas so that we can learn and grow together.
And driven to make a difference, from innovative research to hands-on community support.
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 the resources to pursue their goals, both at work and in their personal lives.
Among our several NJ locations, our Hopewell and Bloomsbury sites are key components of the Biologics Network Strategy, with available Process Development and Analytical Development & Testing opportunities to support the innovating biologics under development.
As a member of the Biologics Manufacturing and Process Development (BMPD) team supporting cross-functional project goals and objectives for biologic drug candidates across all phases of development, the Manager in Program Management Office will manage CMC development teams translating project objectives into effective and detailed project plans to meet business needs, assisting in project execution while interfacing with manufacturing process development, formulation development, regulatory affairs, quality assurance, quality control, supply chain, and analytical staff.
The successful candidate will support the team leads in the development of a detailed project plan including resource planning, tracking project milestones and communication of the project status.
Responsibilities include, but are not limited to:
Manager of Program Management Office will lead/participate in biologics portfolio level activities including business improvement initiatives and resource/budgeting activities.
This individual will also be responsible for contributing to the definition and execution of risk management strategies, contingency planning, supporting the development of a high performing team, and communication of the solutions to managementManager of Program Management Organization within BMPD is a leader, coordinator, and facilitator for the PMO office, capable of assigning and leading projects, providing direction, managing a team, and helping to drive overall direction and strategy for the departmentSr Manager of Program Management Office supports CMC development teams, with one or more molecules in development utilizes a variety of project management tools to build and sustain high-performing cross-functional teams.
Organizes and facilitates project planning, team meetings and project reviews by working closely with the team leaders.
Maintains all program timelines in Microsoft Project or other applicable software and is responsible for communicating changes to the approved plan.
He or she may also work closely with alliance partners for projects that are being jointly developed with a partnerFacilitates and ensures optimal execution against project plans and consistency with the BMS Product Development and Commercialization processEnsures the development teams are practicing the core agile principles of collaboration, prioritization, team accountability, and visibility.
Able to facilitate cross-functional and cross-cultural teams within a matrix organization, and to influence team outputEffectively applies the principles and concepts of project management including timeline, resource and budget aspects.
Proactively communicates project status, issues & risks to management Qualifications Minimum Qualifications:
PhD in a discipline within biotechnological sciences with over three years of experience or a corresponding MS/BS/BA degree with five years of experienceOver three (3) years of technical project management experience in the pharmaceutical industry is required with at least 3 years of experience interacting with cross-functional teamsAdditionally, over three (3) years of biological CMC development experience is preferred with understanding of roles, responsibilities and operational requirements of all functions represented on CMC development teamsPMP certification is desirableWell developed verbal and written communication skills.
Able to read and interpret complex technical communications and present technical strategy and numerical data effectivelyCommunicates ideas in a business persuasive way while ensuring objectivity to all opinionsBecome and remain proficient in all programs necessary to perform the everyday duties of this positionProficiency in MS Office including MS Project is required Bristol-Myers Squibb is an equal opportunity employer - M/F/Vet/DisabilityRequisition ID - 1501265

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