Senior Project Manager

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. 

Responsibilities

  • 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. 

Qualifications 

  • BS Degree required; degree in Engineering preferred.  
  • 4+ years of experience in working as a Project Manager or Team Lead developing products. (i.e.: Experience leading and managing programs, directing cross-functional resources, planning, scheduling.  Budget maintenance and risk mitigation experience a plus). 
  • 3+ years product development within medical device or another regulated industry.  
  • 2+ years working in an R&D environment.  
  • Strong communication and organizational skills.  
  • Experience with delivery of electromechanical platforms.  
  • Life sciences background and/or clinical studies experience preferred.  
  • PMP Certification preferred.