Sr Manager, Program Manager II

2 weeks ago

Salt Lake City, United States BIOMERIEUX, INC. Full time

Description This Program Manager position is with the BioFire Platform Program team and will manage new product development or lifecycle management type projects focused on hardware and/or software development. Program Manager II (PM II) oversees the fulfillment of larger organizational goals in a highly technical environment. They manage a project(s), giving detailed attention to project planning, project budget management, project cross-function coordination, and project execution. Managing a project(s) includes drafting/organizing documentation, overseeing the design history file, running a project meeting, prioritizing projects and goals, regularly updating timelines to track goals and milestones, tracking project budget, facilitating stakeholder communication, guiding the project team through the change management process, and other relevant tasks. PM I/II is competent in design control, change control, and risk management as they relate to medical device development and/or production. PM II is comfortable and/or has experience in leadership positions, both to guide program stakeholders and to serve as a mentor to others on the team. PM I/II may work closely with a project coordinator or less experienced team member and should be adept at delegation and mentorship. Job Responsibilities: * Perform all work in compliance with company policy and within the guidelines of BioFire Diagnostics' Quality System. * Manage project or program communication to align stakeholders and track goals/milestones. * Understand scientific/technical knowledge to support project management requirements. * Run program meetings independently. * Present program-related updates to large groups and executive groups. * Own and delegate program-related tasks, including (but not limited to): meeting minutes, timeline updates, and presentation preparation. * Manages and tracks project or program budget. * Utilizes knowledge of BioFire products, design control, risk management and change control to draft project proposals, design input documentation, project plans, schedules, presentations, technical reviews, etc. * Analyze relevant project information (e.g., project status, project issues, etc.), brainstorm and implement solutions to potential roadblocks. * Maintain documentation; ensure that appropriate documentation is complete at project close. * Own multiple of the following: project plans, design change notices (DCNs), and technical reviews. * Communicate with program stakeholders to set, assess, and meet program milestones. * Facilitate and champion change control efforts in assigned program. * Independently draft risk management plans and/or risk assessments. * Build relationships with (and gain the trust of) program stakeholders. * Gather information on program stakeholders' wants/needs. * Independently manage a large/complex program. * Teach and/or mentor other members of the team. * Navigate design history file (DHF) documentation in an audit (with guidance). * Navigate workflows of other business units/departments to execute a successful project or program. * Collaborate with program team to determine what the future of the program looks like (ensure the needs of other departments are met in this process). * Facilitate collaboration across teams to integrate business goals with program goals. * Identify missing points of view in crucial, decision-making conversations. * Proactively considers plans for self- and peer- training, mentorship, and development. Minimum Qualifications: * Bachelor's degree required * B.S. in life science, engineering, or equivalent technical field a plus * Relevant advanced technical degree or MBA a plus * PMP certification a plus * At least seven years of project or program management experience. Experience working for a medical device ... For full info follow application link. #AdvancedManufacturing

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