Project Manager, Program Management
CR Bard
The Program/Project Manager is responsible for ensuring the success of sustaining engineering programs within the Specimen Management (SM) business at BD. Specifically, We are seeking a highly skilled and motivated Hybrid Agile Project/Program Manager to lead a dynamic cross-functional, hybrid agile team focused on addressing a backlog of projects within our blood specimen collection product group. The successful candidate will have a proven track record in hybrid agile project management, cross-functional team leadership, and a deep understanding of highly regulated environments. This role requires the ability to navigate teams through compliance, supply continuity, and quality projects with a focus on delivering fast, high-quality outcomes. The ideal candidate will be self-directed, coachable, and have a passion for driving excellence in project execution
Lead and motivate a cross-functional, hybrid agile team to successfully deliver compliance, supply continuity, and quality projects for a blood specimen collection product group.
Work with Product Owners and SMEs to decompose a project backlog into a prioritized task backlog.
Optimize value delivered to the organization by planning sprints from the task backlog taking care to plan backward from impact dates and ensuring alignment with organizational goals and regulatory requirements.
Hybrid Agile Project Management:
Implement and champion agile project management methodologies to enhance project efficiency and adaptability.
Foster a collaborative and sprint-oriented project environment, ensuring continuous improvement and responsiveness to changing priorities.
Document and Process Control:
~ Ensure proper phase-gate processes are followed for each project as well as drive the completion of all relevant Design History File and Change Control paperwork.
EDUCATION/EXPERIENCE:
BS degree in Mechanical Engineering, Materials Science & Engineering, Biomedical Engineering or a closely related engineering degree is required. An advanced degree in an engineering discipline or MBA is preferred. Overall 10+ Years of experience is mandatory At least 8 years relevant experience in product development and design, experience in medical devices/products is a plus. Minimum of 5 years project management experience. Experience in medical device industries required, including experience in FDA or other regulated environments required. Ability to take disparate data points and make sound business decisions and bring clarity to ambiguous situations. Program Management Professional Certificate PreferredHas successfully completed design change activities for medical devices.
Experience developing Class II medical devices.
Experience utilizing combination of analytical, statistical, computational, and empirical methods to gain deep understanding of design and minimize overall development timelines.
Work Shift
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