Head of Product & Project Management

Ultradent, the global name in oral health, is seeking a Project Manager to join Ultradent's growing R&D Product Sustainment team.The Project Manager is a fundamental contributor to business growth, helping drive increased gross margin and net revenue both domestically and globally. If you have a background in project management within manufacturing, R&D product development or sustainment, life sciences, medical device, regulatory compliance, or other regulated industries—and thrive in a cross-functional environment—we encourage you to apply.The R&D Product Sustainment Project Manager is responsible for overseeing changes to existing products and processes. They are also responsible to plan projects to meet timeline, budget, and quality requirements, as well as represent the interests of all disciplines within the organization while implementing changes to products that are currently on the market.The Project Manager is also expected to encourage safe practices and enforce safety policies, in addition to:Developing and monitoring project risk management plans, resolving any issues that may arise during the project life cycle, interpreting situations/ issues into compliant paths with regards to FDA, ISO, and Ultradent standards.Execution of project meetings, ensuring project deliverables are well understood, and actions are agreed upon, communicated, and followed up.Stand as first point of call for new projects, status reports and guidanceProvide updates as necessary to all project stakeholders, monitoring components of activity to ensure project deliverables are met within scope, resource, time, cost, and quality.Coordinate with Business Unit and Brand Marketing teams over launch formats/volumes/timings to agree upon achievable launch plans.Create project and quality system documentation for new products/processes and changes to existing products/processesWHAT YOU’LL NEED TO SUCCEED:Bachelor’s Degree or a combination of education and 1-3 years of experience working with medical devices sufficient to perform essential duties is idealStrong understanding of regulatory guidance relevant to medical device, specifically FDA’s CFR820.30 and ISO 13485:2016 is ideal1-3 years of experience leading cross-functional teams as a project manager, preferably in bringing new products to commercialization successfully is preferredPMI PMP Certification preferredWHAT WE’RE LOOKING FOR IN YOU:Ability to effectively manage projects under low levels of supervisionExcellent communication skills (oral and written). Ability to communicate complex information to various departments throughout the companyAbility to use quantitative as demonstrated from past work experienceAbility to effectively use various computer software including Microsoft Office Suite (Word, Excel, Visio, Power Point), Smartsheet, and Oracle ERP system (including Agile PLM).Our core values - Integrity, care, quality, innovation, and hard work- guide us daily. VEVRAA Federal Contractor: For more information please contact us at View email address on click.appcast.io: Salt Lake City, UTType: Full time