General Responsibilities

Project Initiation, Planning, Execution and Monitoring, Closing

• Define project scope, objectives, deliverables, and success criteria in collaboration with stakeholders
• Planning, execution, monitoring of software and hardware new product development projects for medical devices using a hybrid approach, integrating agile methodologies for software innovation and waterfall frameworks for hardware development
• Develop comprehensive project plans, encompassing timelines, budgets, and resource allocation
• Monitor project progress, identify and manage risks, and implement contingency plans to ensure objectives are met
• Plan and monitor assigned budget
• Ensure adherence to design controls and product development processes

Cross-functional collaboration

• Ensure effective identification and communication of goals, progress, risks and issues

Regulatory and Compliance Oversight

• Ensure all project activities adhere to medical device regulatory requirements (e.g. ISO 13485)
• Maintain documentation in compliance with quality management systems

Skills and Experience

• Bachelor’s degree in engineering, Business, or related field
• Project Management Expertise: some years managing end-to-end product development projects in the medical device industry is a "must"
• SW Project Management Knowledge: Familiarity in project management of Medical Device Software (according to IEC 62304)
• Regulated Industry Knowledge: Familiarity with product development processes, including design controls, in compliance-driven environments
• Collaboration & Communication: Strong interpersonal and motivational skills to foster teamwork and alignment across functions and levels
• Problem-solving: Resilience, adaptability, and a proactive approach to navigating challenges
• Technical Proficiency: Experience with project management methodologies (e.g., Agile, Waterfall) and tools like MS Project or similar platforms
• Prior experience in product development or engineering within the medical device industry
• Basic understanding of medical device standards and regulations
• PMP certification is desirable
• Scrum Master experience is desirable
• Fluent English language skills, written and spoken

What we can offer you

In addition to providing you with a supportive, inclusive and collaborative environment where you will feel empowered to take ownership and drive meaningful change, we will reward you with the following:

• A dynamic role in an advanced Medical Device environment interfacing with all worldwide regulatory landscapes supporting your professional career growth
• Exposure to a State-of-the-Art medical device development process, in close co-operation with international clinicians
• Competitive base salary
• Variable short-term & long-term incentives
• Recognition: through our STARS Program, we recognize and celebrate our colleagues’ contributions and achievements

If you like the sound of the above and feel energized by the idea of joining a great brand at a moment of exciting expansion, please apply now. We look forward to hearing from you!