Program Management - Digital Medical Devices - Remote ...
Softworld, a Kelly Company - philadelphia, PA
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Job Title: Medical Devices Program ManagerUnit: Surgical Research & DevelopmentLocation: RemoteDuration: 6-12 MonthsJob Objectives PurposePlan and oversee the allocation of resources and coordination of activities related to the development of surgical digital medical devices within Surgical R&D, utilizing the global Product Development Process (PDP), associated systems, and tools.Key Activities ResponsibilitiesLead Project Execution: Oversee the creation and execution of the project plan, work breakdown structure, timeline (MS Project), budget, and capital plan as needed. Adjust budget forecasts as necessary.Provide Expertise: Offer technical insight and project management proficiency to various program areas to ensure proper focus and progress.Project Leadership: Act as the program leader for ophthalmic digital medical device projects (including Cloud-based software and user applications).Collaborate with Stakeholders: Work closely with the Commercial team and key project members to gather Voice of Customer (VOC) insights for product design and development.Team Management: Oversee team activities using Agile software development methodologies such as Sprint and Scrum.Business Case Development: Partner with the Commercial team to develop business cases for new projects, including forecasts, cost estimates, pricing, and development expenses.Resource Coordination: Identify and negotiate functional resources to build an appropriate cross-functional project team.Risk Management: Create and maintain project and technical risk assessments. Identify risks, develop mitigation strategies, and manage risks to resolution.Effective Communication: Keep R&D management, Commercial, Quality, Regulatory, and other relevant functions informed of project status and aligned with project deliverables.Issue Escalation: Alert management promptly of any issues that may delay project timelines, enabling timely action. Propose solutions to minimize project impact.Design Compliance: Plan, coordinate, and conduct formal and informal project design reviews for compliance. Document design inputs, outputs, and verification.Ensure Quality Compliance: Ensure adherence to all current quality system requirements concerning design control.Skills, Knowledge, and AbilitiesProgram Management Experience: Experience in managing cloud-based medical device development is highly preferred.Familiarity with Cloud-based technologiesEducational Background: Bachelor's Degree in Engineering, preferably in Computer Science, IT, or a related engineering discipline.Certifications: PMP certification is desired.Advanced Qualifications: An advanced degree is a plus but not mandatory.
Created: 2024-07-07