Medtronic

Senior Project Manager, Product Development – Neuromodulation and Pelvic Health

Medtronic

full-time

Posted on:

Origin:  • 🇺🇸 United States • Colorado

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Salary

💰 $112,000 - $168,000 per year

Job Level

Senior

Tech Stack

PMP

About the role

  • Lead and coordinate complex product development and sustaining projects for Neuromodulation and Pelvic Health
  • Initially focus on projects associated with Emprint Ablation systems and related products
  • Manage projects in released product space including regulatory compliance remediation, manufacturing capacity expansion, product design enhancement, and supply continuity programs
  • Lead or leverage cross-functional teams to evaluate, develop and manage projects for new product development and lifecycle management
  • Oversee and manage operational aspects of ongoing projects and serve as liaison between project management/planning, project team, and line management
  • Manage development and implementation processes involving departmental or cross-functional teams
  • Review project status and budgets; manage schedules and prepare status reports
  • Monitor projects from initiation through delivery and assess issues, developing resolutions to meet productivity, quality, and client-satisfaction goals
  • Develop mechanisms for monitoring project progress and for intervention/problem solving
  • Gather requirements, plan requirements elicitation and requirements management to meet stakeholder demands
  • Communicate with stakeholders and obtain stakeholder engagement to ensure end products/processes solve business problems
  • Work closely with cross-functional teams to ensure goals are delivered on time, within scope, and in compliance with quality and regulatory standards
  • Work onsite 4 days per week as part of a hybrid flexible work arrangement

Requirements

  • Bachelor’s degree in Engineering, Life Sciences, Business, or a related field
  • Minimum of 4 years of experience in project management, product development, or a related field
  • Or advanced degree with a minimum of 2 years experience
  • Proven track record of successfully managing complex projects in a cross-functional environment (preferred)
  • Strong understanding of product development processes, including Design Control (preferred)
  • Proficiency in project management tools (e.g., Microsoft Project, Smartsheet) (preferred)
  • PMP or equivalent certification (preferred)
  • Experience in the medical device industry or other regulated industries (preferred)
  • Familiarity with FDA and ISO requirements (preferred)
  • Advanced degree (e.g., MBA or MS in Engineering) (preferred)
  • Excellent leadership and communication skills
  • Strong problem-solving and decision-making abilities
  • Ability to manage multiple priorities in a fast-paced environment
  • Detail-oriented with a focus on quality and compliance
  • For Office Roles: ability to be independently mobile, interact with a computer, and communicate with peers and co-workers
  • For sales reps and patient facing field employees: comply with hospital credentialing requirements
  • Employer participates in the federal E-Verify program to confirm identity and employment authorization