Senior Director R&D Portfolio and Program Management

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7izcx9

Senior Director R&D; Portfolio and Program Management

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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 13485, 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 MedTech or xkiyazw 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 14971 risk management

Ability to synthesize business, technical, regulatory, and operational factors across large programs

Knowledge of EU MDR, CE Marking, ISO 13485; 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

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7izcx9