Work Flexibility Hybrid What You Will Do Lead end-to-end execution of complex mechanical and electro-mechanical R D programs from concept through commercialization Own and manage integrated project plans covering scope schedule cost quality risks and dependencies Drive disciplined execution using phase-gate PDP frameworks while ensuring Design Control compliance Partner with cross-functional teams Engineering Quality Regulatory Manufacturing Supply Chain Clinical Marketing across global sites Proactively identify assess and mitigate technical regulatory supply chain and schedule risks Develop and manage project budgets resource plans procurement strategies and supplier engagements Lead governance activities including design reviews phase-gate reviews executive updates and escalation forums Act as the primary communication and alignment hub influencing stakeholders without direct authority and keeping the customer patient at the center What You Need Basic Qualifications Bachelor s degree or equivalent in Engineering or a related technical discipline Minimum 8 years of experience managing technical or R D projects Demonstrated experience leading cross-functional teams in a matrixed setting Strong foundation in project management fundamentals scope schedule cost risk quality Ability to communicate clearly and effectively with technical teams and senior stakeholders Preferred Qualifications PMP certification or equivalent formal project management credential Experience in medical device regulated product development or highly regulated industries Working knowledge of FDA ISO 13485 and Design Control DHF requirements Strong background in mechanical or electro-mechanical product development programs Proven ability to influence without authority manage ambiguity and drive results under pressure Travel Percentage 20