Senior Project Management, Software PMO

Make a meaningful difference to patients around the world. Our project management teams support many parts of Edwards. You’ll be a trusted thought leader as you ensure our projects are completed efficiently and effectively. Your strategic mindset and fresh perspectives will be an essential part of how we bring innovative solutions for patients.

How You Will Make An Impact

• Manage all phases of the project life cycle, from initiation to closure.
• Lead cross-functional teams (R&D, Operations, Quality, Regulatory) to develop and measure progress against goals and objectives.
• Establish and maintain relationships and communication with team members and stakeholders.
• Manage project schedules and identify/resolve conflicts to maintain the schedule.
• Execute tasks as defined in the project management plan and actively manage risks.
• Measure project performance, identify variances, and implement corrective actions.
• Collaborate with hardware, firmware, mechanical, and software engineering leaders to ensure successful execution and delivery of the device.
• Develop detailed engineering plans that support manufacturing and OEM integration.
• Collaborate with OPS teams and external OEM partners to understand requirements and drive execution to meet the plan.
• Identify and remove obstacles to unblock team execution and balance competing priorities.
  
  

• 5 years of experience as a Project Manager/Program Manager in Software or Hardware field
• Bachelor's degree or equivalent
• Experience managing complex projects, preferably in the medical device industry.
• Strong technical skills and ability to understand technical designs, software development lifecycle, challenges, and risks; ability to work closely with engineers
• Expertise in using MS Office Suite and related project management systems
• Proficiency in English (written/verbal/reading)
• Excellent documentation and communication skills and interpersonal skills
• Practical familiarity with Agile and Waterfall methodologies and ability to apply them as needed.
  
  

• PMP course
• Medical Device industry knowledge
• Experience with medical device regulatory standards and integration processes