Head of Device Product Development
2 settimane fa
Parma, Provincia di Parma; Emilia-Romagna, Italia
Chiesi
Tempo pieno
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Overview In this role, you will lead the Device Product Development department to advance Medical Devices and device constituents in drug-device combos, ensuring feasible design, development, manufacturing and testing within quality and regulatory standards. You will shape strategies from prototyping to product launch, drive innovative device technologies, and manage partnerships with vendors and manufacturing partners. You will influence the project portfolio, resources, and compliance, while developing a high-performance, cross-functional team in a global R&D context. Retribuzione / Benefits
pension
private medical insurance
flexible benefits programme
annual bonus scheme
relocation support
Lead and develop the Device Product Development team, ensuring alignment with quality, cGMP, HSE and regulations
Identify optimal design, development and manufacturing strategies from prototyping to launch
Foster innovative device products and testing technologies aligned with company strategy
Participate in due diligences for in-licensing opportunities
Support IP strategy and patent development
Manage strategic vendor relationships (design agencies, CMOs, test labs, consultants)
Ensure successful transfer of device products and specs to Manufacturing or CMOs
Oversee staff development, capability building and resource allocation
Act as centre of excellence for medical devices and combination products balancing internal capacity and outsourcing
Contribute to device project portfolio, resources (CAPEX, OPEX, FTE) and management communications
Ensure safety and environmental compliance
Provide expertise in medical device quality, risk management, manufacturing and regulatory frameworks (ISO 13485, ISO 14971, cGMP)
Substantial leadership experience in drug-device combination product development
Experience in managing, coaching and developing teams
Proven ability to lead multidisciplinary organizations through growth and transformation
Accountability for strategic R&D activities from concept to commercialization
Strong scientific and engineering foundation with hands-on industrial experience
Ability to operate at the intersection of innovation, quality, regulatory requirements and business objectives
Effective communication and collaboration across diverse teams
Fluent in written and spoken English
stakeholder management
collaboration
medical device quality (ISO 13485)
risk management (ISO 14971)