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Myomo is seeking a strong Senior Project Manager who will play a central role in the execution of both NPD and sustaining pipeline strategies, ultimately developing and delivering Myomo’s rehabilitation products. The Senior Project Manager will lead and inspire the cross-functional team to create innovative, meaningful, business-impactful products, and ensure that their programs successfully navigate the design controls process and deliver high-quality products to market.
Job Responsibility:
Manage elements of new product development and/or sustaining processes, working cross-functionally through phase gate development
Direct and lead activities related to the MyoPro electro-mechanical orthotic solution
Manage the cross-functional team, maintaining responsibility for project plans, schedules, risk mitigation, and resource/ material management
Collaborate with manufacturing, operations, marketing, sales, product management, quality, regulatory and clinical functions to ensure stakeholder needs are met
Identify the critical project path, scheduling resources accordingly to remove impediments, obstacles, and blockers and resolve scheduling delays for the team
Plan and manage scope, objectives, project/phase steps/gates based on QMS, SOPs, and project compliance with QMS
Coach and develop team members towards meeting corporate and personal objectives
Direct alignment with PMO team and ensure execution with proper resources (skills, abilities, and talent)
Contribute to project expense planning and resource management as needed
Requirements:
BS Degree required
degree in Engineering preferred
5+ years of experience in working as a Project Manager or Team Lead developing products
3+ years product development within medical device or other regulated industry
Strong organizational and cross-functional communication skills
Experience with delivery of electromechanical or other complex technological platforms
Nice to have:
Budget maintenance and risk mitigation experience
Oversight of agile or hybrid software development processes
Medical device industry experience and/or PMP Certification