Scrum Master – Clinical Imaging Application (Plymouth, MN)
Philips
Job Title Scrum Master – Clinical Imaging Application (Plymouth, MN)Job DescriptionScrum Master – Clinical Imaging Application (Plymouth, MN)You will join a dynamic and high-performing global software team within the Image Guided Therapy Devices (IGT-D) Software R&D group based in Plymouth, MN. In this role, you will facilitate the development of innovative features for our Intravascular Ultrasound (IVUS) Clinical Imaging Application, which significantly enhances the clinical workflow for our physician customers and positively impacts patients’ lives.Your role:Leading and coordinating Scrum ceremonies and practices, e.g., Backlog refinement, Sprint Planning, Daily stand-ups, Sprint Reviews and Retrospectives as well as facilitating periodic synchronization meetings, including Scrum of Scrums / ART (Agile Release Train) sync at the Program level and the Value Stream sync for Solution Trains.Coordinating and managing dependencies between Software, Hardware and other workstream teams to help remove impediments while ensuring all work is tracked in the backlog and evenly balanced across team members.Monitor and report on team’s progress in the execution of features and capabilities. Facilitate and encourage agile behaviors, reinforcing practices, norms, ceremonies, and supporting the overall team performance and efficiency.Effectively facilitate unbiased open discussions, encourage active listening, ensure all voices are heard and ask open ended questions. Identifying team improvement opportunities and applying best practices to support continuous improvement.Coach and mentor the team on Lean Agile principles and guide the team on how to use scrum with Scaled Agile Framework (SAFe).You’re the right fit if:You’ve acquired 5+ years of professional experience in a Scrum Master role with at least 2 years of experience working in Scaled Agile Framework (SAFe).Your skills include using tools like Jira, Azure DevOps, Confluence, MS Teams while working with global software development teams.You have experience working in an FDA regulated Software as a Medical Device (SaMD) and/or Software in a Medical Device (SiMD) projects and with regulatory standards like IEC 62304, 82304, ISO 13485, ISO 14971.You have a Bachelor’s degree or equivalent experience, preferably in a technical discipline.You’re an excellent communicator, presenter, and leader as well as a strong analytical problem solver. You also have the ability to work effectively in a fast-paced, dynamic environment.You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this .Additional Information:US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.Company relocation benefits will not be provided for this position. For this position, you must reside in or within commuting distance to Plymouth, MN.About Philips:We are a health technology company. We built our entire company around the belief that every human matters, and we won’t stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others.Learn more about .DiscoverLearn more aboutRead more about .If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our commitment to diversity and inclusion .#LI-PH1#LI-HYBRIDThis requisition is expected to stay active for 45 days but may close earlier if a successful candidate is selected or business necessity dictates. Interested candidates are encouraged to apply as soon as possible to ensure consideration.Philips is an Equal Employment and Opportunity Employer/Disabled/Veteran and maintains a drug-free workplace.
Plymouth
Thu, 29 Aug 2024 01:20:11 GMT
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