Bachelor's degree in Engineering, Life Sciences, Business, or a related field.
5+ years of project management experience, preferably within the medical device, life sciences, or regulated healthcare industry.
Strong working knowledge of EU MDR (Medical Device Regulation 2017/745) requirements.
Demonstrated experience using Smartsheet for project scheduling, resource planning, workflow management, and reporting.
Ability to build and manage Smartsheet dashboards for executive and program review meetings.
Experience leading cross-functional teams and managing complex projects with multiple stakeholders.
Strong risk management, planning, organizational, and communication skills.
Proficiency with Microsoft Office Suite, including Excel, PowerPoint, and Teams.