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Project Manager, Portfolio Optimization - Charlotte, NC
Project Manager, Portfolio Optimization - Charlotte, NC-February 2024
Usa Home Office
Feb 11, 2026
About Project Manager, Portfolio Optimization - Charlotte, NC

  Dentsply Sirona is the world’s largest manufacturer of professional dental products and technologies, with a 130-year history of innovation and service to the dental industry and patients worldwide. Dentsply Sirona develops, manufactures, and markets a comprehensive solutions offering including dental and oral health products as well as other consumable medical devices under a strong portfolio of world class brands. Dentsply Sirona’s products provide innovative, high-quality and effective solutions to advance patient care and deliver better and safer dentistry. Dentsply Sirona’s global headquarters is located in Charlotte, North Carolina. The company’s shares are listed in the United States on NASDAQ under the symbol XRAY.

  Bringing out the best in people

  As advanced as dentistry is today, we are dedicated to making it even better. Our people have a passion for innovation and are committed to applying it to improve dental care. We live and breathe high performance, working as one global team, bringing out the best in each other for the benefit of dental patients, and the professionals who serve them. If you want to grow and develop as a part of a team that is shaping an industry, then we’re looking for the best to join us.

  Working at Dentsply Sirona you are able to:

  Develop faster - with our commitment to the best professional development.

  Perform better - as part of a high-performance, empowering culture.

  Shape an industry - with a market leader that continues to drive innovation.

  Make a difference -by helping improve oral health worldwide.

  Do you enjoy leading projects, connecting others and driving for results? Do you enjoy partnering with nearly all functions across the globe to achieve a common goal?

  Our Project Manager is responsible for creating project plans, timelines and associated budgets for full life cycle management for products within assigned business unit:

  New product and program development through launch

  Sustaining engineering projects

  Obsolescence of existing products to streamline portfolio.

  This role partners frequently with our marketing, regulatory, supply chain, quality, regulatory and commercial teams by ensuring we have the right resources allocated, right timelines associated and the right budget for various global projects.

  Lead the optimization of regional product mix, product lifecycle management, and obsolescence of existing products to streamline portfolio

  Establish clear directions, set stretch objectives and lay out project plan in a well-defined and organized manner

  Organize schedule and facilitate cross-functional team meetings across domestic and international sites to exchange information, identify risks, chart progress, and promote collaboration

  Clearly and effectively communicate project plan, timeline, budget and corresponding target dates to key stakeholders within a timely manner, ensuring the strategy is clearly understood and executed

  Ownership of Accolade compliance with corporate expectations Ensure all phases and stage gates are completed on time and on budget for Class 1, 2 and 3 medical devices.

  Direct responsibility for project/program scope, schedule & budget(s) to balance business deliverables within resource and time constraints

  Identify and resolve emerging issues that may impact project, department or corporate goals

  Recognize potential threats to project success and elevate issues to leadership.

  Present project status updates to senior leadership

  Maintain and routinely update Project Management systems to track project progress, monitor project budget, report project status, and analyze results against objectives, e.g. SharePoint, TEAMS, Microsoft Project, Accolade, etc.

  Facilitate the exchange of required information and documentation and lead collaborative meetings and teleconferences between internal Dentsply Sirona, outside suppliers and contract manufacturers to resolve issues and technology transfer.

  Assemble, manage and lead international multidisciplinary project teams to advance the development, submission, approval and launch of new products

  Ownership of detailed project timeline for all NPD activities. Define the scope of work for each new project, clearly identify tasks and responsibilities for all project team members and establish target completion dates for key project milestones.

  Identify resource conflicts early, and discuss (negotiate) with Consumable and site leadership.

  Ownership of Accolade compliance with corporate expectations.

  Organize and facilitate cross-functional team meetings across domestic and international sites to exchange information, identify risks, chart progress, and promote collaboration.

  Interface with department managers and senior management to facilitate allocation and prioritization of resources necessary to achieve objectives within established timelines.

  Maintain and routinely update Project Management systems to track project progress, monitor project budget, report project status, and analyze results against objectives (i.e., SharePoint, MS Teams and/or Project, Accolade)

  Facilitate the exchange of required information and documentation and lead collaborative meetings and teleconferences between internal Dentsply Sirona, outside suppliers and contract manufacturers to resolve issues and technology transfer.

  Identify and resolve emerging issues that may impact project, department or corporate goals. Recognize potential threats to project success and elevate issues to leadership.

  Conduct lessons learned, Stage Gate Reviews and project close-out sessions to obtain information that can be used to improve future projects. Contribute to the Dentsply Sirona Project Management knowledgebase through development and revision of project management tools and templates.

  Maintain industry knowledge for global Project Management best practices

  Understand, embrace and ensure compliance of relevant Quality Systems and applicable government and industry regulations

  Conduct project activities within the framework of the group’s ISO 13485 Quality Systems

  EDUCATION and/or EXPERIENCE

  BS Degree in Business, Engineering, Physical Sciences or equivalent

  Project Management Professional (PMP) Certification strongly preferred

  Minimum 6 years’ experience leading projects (develop, launch, sustaining engineering/maintenance, and sunsetting), preferably in medical device industry

  Working knowledge of FDA and ISO medical device development regulations to ensure that these can be built in project timeline and scope

  Proficient in Microsoft Excel, PowerPoint, Word and Project and Accolade and SmartSolve

  Ability to collaborate with global team members in varying time zones

  Demonstrated ability to work effectively in a matrix environment and influence across matrix with global, regional and country partners

  Ability to travel international and domestic, up to 15%

  ADDITIONAL EXPERIENCE

  Ability to establish clear directions, set stretch objectives and lay out project plan in a well-defined and organized manner

  Dedicated to providing enterprise-wide common systems for designing and measuring work processes

  Committed to continuous improvement through empowerment and management by data

  Creates a learning environment leading to the most efficient and effective work processes

  Ability to influence others and self to drive for results

  Ability to quickly find common ground and ensure cooperation with cross functional partners

  Strong written and oral presentation skills, with the ability to engage, inspire, build credibility and engender trust across all levels of an organization.

  Ability to filter and distill relevant information for a specific audience.

  Demonstrated ability to execute all aspects of the project management process from initiating, scoping, planning, executing, monitoring, controlling, closing and learning for multi-disciplinary teams

  #LI-JV1

  Dentsply Sirona is an Equal Opportunity/ Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, disability, or protected Veteran status. We appreciate your interest in Dentsply Sirona.

  If you need assistance with completing the online application due to a disability, please send an accommodation request to careers@dentsplysirona.com (careers@dentsply.com) . Please be sure to include “Accommodation Request” in the subject.

  For California Residents:

  We may collect the following categories of personal information in connection with the submission of your resume or application materials to us for employment, and if hired, your employment with us: identifiers (e.g., name, address, email address, birthdate); personal records (e.g., telephone number, signature, education information, criminal background information, passport number and visa information); consumer characteristics (e.g., sex, marital status, veteran status, race, disability, sexual orientation); professional or employment information (e.g., resume, cover letter, employment history, background check forms, references, certifications, transcripts and languages spoken); and inferences from personal information collected (e.g., a profile reflecting abilities and aptitudes).

  The above categories of personal information are collected for the following business purposes: performing recruitment and hiring services; processing interactions and transactions (e.g., to comply with federal and state laws requiring us to maintain certain records, managing the workforce); and security (e.g., detecting security incidents, protecting against fraudulent or illegal activity).

  For additional details and questions, contact us at careers@dentsplysirona.com

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