Project Manager Medtech Neurovascular

Johnson & Johnson Johnson & Johnson · Pharma · Irvine, CA +2

Project Manager for Medtech Neurovascular at Johnson & Johnson, focusing on strategic oversight and process governance for medical and regulatory documentation. Responsibilities include project planning, metrics tracking, risk management, and implementing process improvements to enhance team efficiency and communication. The role requires experience in project management systems and the medical device industry, with a focus on clinical evaluations and regulatory documentation.

What you'd actually do

  1. Leads end to end project management activities including project plan development, dashboard generation, metrics tracking, risk identification and mitigations, resource planning, and development of communication strategies.
  2. Ensures timelines are met and practices are being consistently deployed across the global organization.
  3. Maintains knowledge and access to applicable J&J MedTech Quality Systems to support the team in document retrieval and routing of documents for approval.
  4. Maintains and monitors metrics relevant to the assigned activities and communicates business related issues or opportunities to next management level to enable corrective and preventive action to be taken as needed.
  5. Sets up and leads meetings for project execution per project plan, as well as meetings in support of the overall project management process.

Skills

Required

  • Proficiency in Microsoft Applications (Word, Excel, Outlook, Teams, and PowerPoint) and Adobe Acrobat
  • Proficiency with project management methodologies and project planning tools such as Wrike, MS Project, or Smartsheet.
  • Exceptional communication and social skills across different organization levels.
  • Excellent analytical, problem-solving, and decision-making abilities.

Nice to have

  • advanced degree is preferred
  • Experience within the medical device industry and knowledge of CER regulatory requirements, evidence generation, and state of the art and systematic literature review creation is preferred.
  • Experience in resource coordination with respect to processes and outcomes.
  • Experience with WRIKE or project management systems is preferred.
  • Process Excellence training or certification preferred.
  • Project Management Professional (PMP) certification preferred.

What the JD emphasized

  • Minimum of 7 years of related job experience is required.
  • Experience within the medical device industry and knowledge of CER regulatory requirements, evidence generation, and state of the art and systematic literature review creation is preferred.