Senior Director R&D Portfolio And Program Management

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Senior Director R&D; Portfolio and Program Management
As Senior Director, you will lead the CP R&D; portfolio and PMO, guiding capital equipment programs and product development.
You'll shape governance, prioritization, and resource planning across global teams, driving on-time delivery within budgets and regulatory timelines.
You'll chair the Portfolio Review Committee and partner with CP leadership to optimize portfolio trade-offs and investments.
You'll manage a ~10-person organization across multiple European sites and report to the VP of CP R&D.;
This role blends strategic oversight with hands-on execution to advance life-changing medical innovations.
Private medical insurance Employee stock purchase plan Global recognition programme Flexible working options Competitive compensation Provide strategic oversight of CP Director, Project Heads and Senior Project Managers, ensuring disciplined execution and accountability for timelines, budgets, milestones, and deliverables Lead and develop direct reports and teams, establishing clear accountability and succession planning across CP R&D; project leadership Oversee portfolio risks, interdependencies, and mitigation to protect timelines and budgets Guide project teams to proactively resolve barriers ensuring governance commitments are met Chair PRC governance meetings and prepare executives for reviews and updates Establish and improve the CP R&D; portfolio operating model, governance cadence, escalation pathways,



and standardized practices Develop executive dashboards and decision materials showing milestones, budget, resources, risks, and dependencies Partner with cross-functional leaders to evaluate trade-offs, resource constraints, investment priorities, and sequencing Monitor budgets and resources, providing financial reporting and risk insights to CP R&D; leadership Facilitate stakeholder alignment through clear communication and regular updates Ensure regulatory and quality alignment with ISO *****, EU MDR, CE marking and design controls Drive process improvement using lean methods and design thinking across the maturity curve Lead continuous improvement efforts to raise process maturity across functional areas Extensive experience leading complex R&D; programs and PMO functions in Med Tech or regulated industries Proven track record managing large-scale NPD/NPI programs in a global, matrixed environment Senior people leadership for Director-level project leaders with performance coaching Broad technical knowledge in medical technology, including design controls and ISO ***** risk management Ability to synthesize business, technical, regulatory, and operational factors across large programs Knowledge of EU MDR, CE Marking, ISO *****; regulatory sensitivity is preferred Experience with portfolio governance, capacity planning, executive dashboards, and trade-off recommendations BS in engineering, science, business, technology or equivalent; PMP or similar certification preferred Travel approx.
30% to Europe and global sites #J-*****-Ljbffr

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7imr7b