Senior Manager, Regulatory Affairs role at Cencora focused on leading medical device regulatory projects and providing expert consultancy to clients. The position requires deep regulatory expertise, medical technology knowledge, and ability to manage complex projects while maintaining client relationships and supporting business growth.

Responsibilities

- Lead planning and execution of client projects to agreed KPIs, timelines, budgets, and quality standards
- Coordinate project teams and provide expert regulatory consultancy to clients and Health Authorities
- Prepare, review, and compile project documentation for medical device and diagnostics assignments
- Build and maintain client relationships while identifying opportunities for expanded service support
- Deliver seminars, presentations,



and educational content for colleagues, clients, and professional audiences

Requirements

- Proven in-depth professional experience in regulatory affairs or medical device services
- Strong expertise in medical technology and veterinary products
- Demonstrated experience supporting medical advice activities with essential medical advice skills
- University degree in Science or Engineering
- Proven ability to lead complex project delivery in specialist environments
- Business fluency in English and relevant local language
- Strong project management and stakeholder relationship skills

📌 Senior Manager, Regulatory Affairs (España)
🏢 Cencora
📍 España