Principal Project Management Specialist

Principal Project Management Specialist Lead massive-scale, flow-purposeful projects in Medtronic’s product improvement area. You’ll oversee tasks from inception thru release, making sure product fine, regulatory compliance, and nicely timed transport.

🔧 Key Responsibilities

• Project Leadership: Drive new product improvement and lifecycle management via move-realistic corporations (R&D, Quality, Ops, Regulatory)
• Planning & Tracking: Build focused project plans, manipulate schedules, budgets, assets, and song progress 
• Risk & Issue Management: Identify risks, create mitigation strategies, and clear up issues to satisfy first-class and productiveness dreams
• Stakeholder Communication: Provide everyday popularity updates, facilitate choice-making, and hold leadership engaged .
• Regulatory Adherence: Ensure compliance with layout controls and medical device standards (e.G., IEC, ISO)
• Mentorship: Coach and guide junior body of workers and likely lead crew initiatives 

🎓 Qualifications

• Bachelor’s degree required; superior diploma preferred.
• Typically 7–10+ years managing complex, regulated product development initiatives—or 5+ years with advanced diploma.
• PMP certification and familiarity with Lean/Six Sigma are a plus.
• Experience with scientific device merchandise—in particular in cardiac or surgical tech—is useful. 
• Proficient in venture tools like Microsoft Project or ProChain.

💼 Why It Matters

Medtronic’s undertaking is to relieve pain, repair health, and expand life. This role ensures that life-changing scientific gadgets are evolved correctly, accurately, and in compliance with global necessities—right now impacting patient effects.