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 environment.
• 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.