Myomo, Inc. | Program Manager | burlington, vt

1 month ago

burlington, United States Myomo, Inc. Full time

Have you ever felt blown away by the miracles of modern medicine, while also feeling that the patient experience still leaves much to be desired?


Here at Myomo, Inc., it's our mission not only to leverage the power of cutting-edge robotic technology to improve patient quality of life, but also to demonstrate a commitment to prioritize and serve the patient.


We are 1st in the U.S. to develop and market the MyoPro® product line of lightweight, non-invasive, powered arm braces (orthoses) to restore function in the paralyzed or weakened arms and hands of individuals that have suffered a stroke, spinal cord or nerve injury such as brachial plexus injury, or other neuromuscular disability such as traumatic brain injury, (TBI) brachial plexus injury, (BPI) or multiple sclerosis (MS). It is the only device that, sensing a patient’s own neurological signals through non-invasive sensors on the arm, can restore their ability to use their arms and hands so that they can return to work, live independently and reduce their cost of care.


At Myomo, we are driven by a mission to enable independence and confidence for stroke survivors as well as those living with the impact of another neurological disorder. Our teams continue to break through barriers, defining the limits of what is possible in both medical device robotics and our global system of care.


We're currently seeking a strong Program Manager, who will play a key role in conveying innovative, meaningful, and business-impactful products, ensuring that programs successfully navigate Myomo's design controls process to ultimately deliver high-quality products to market.


The ideal candidate loves to build cross-functionally, and would bring both discipline (execution) and inspiration (iterative improvement) to the role. He/she would possess a results-driven orientation, developed business acumen, and strong attention to detail as well as a proven track record of collaborative success.


Responsibilities


  • Manage elements of the new product development process, working cross-functionally to support Myomo’s phase gate development process.
  • Support delivery of results cross-functionally, driving projects forward via complex system design trade-offs, program and product risk mitigation, technical problem solving, and implementation decisions.
  • Direct alignment with the Director of PMO to ensure execution with proper resources. (skills, abilities, and talent)
  • Assist in selecting, and developing, personnel to ensure the efficient operation of the cross-functional team.
  • Understand and effectively partner with Manufacturing/ Operations, Marketing, Sales, Quality, Regulatory and Clinical functions.
  • Direct and control activities related to MyoPro’s Electro-mechanical orthotic solutions.
  • Provide functional and/or project vision, as well as group leadership toward setting and meeting business goals affecting the success of the company.
  • Provide project expense planning and resource management as needed across the organization.
  • Partner with Product Management to work through user and business needs.
  • Interface with Clinical and Research teams to ensure project solutions meet user needs.
  • Collaborate with Quality/Regulatory, assuring that product development meets all requirements of design controls.
  • Ensure that Manufacturing is involved throughout the development process and is a key voice to making a successful transition from medical device development to the launch.
  • Perform other similar duties as assigned.


Requirements


  • Bachelor’s degree in Engineering (Biomedical, Mechanical or Electrical/Software) or life sciences (Biology, Chemistry)
  • 7+ years of experience working as a Project Manager developing products. (i.e.: Experience leading and managing programs, directing cross functional resources, planning, scheduling, budget maintenance, and risk mitigation)
  • 5+ years of the project management experience needs to be in the medical device, biotechnology or pharmaceutical industries.
  • 3+ years working in a product development environment (desirable)
  • 3+ years working with electromechanical systems (desirable)
  • PMP Certification (desirable)
  • Ability to effectively manage and prioritize multiple projects and work independently with minimal supervision.
  • Critical thinking, analytical and problem-solving abilities.
  • Excellent verbal/written communication and organizational skills.

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