End-to-end project management: planning, execution, monitoring, and reporting.
Leading a multidisciplinary development team (mechanical, electrical, and software).
Hands-on work in design, testing, and product improvements.
Managing and coordinating activities between company teams and external suppliers.
Developing R D strategies, including initiating innovative ideas and process improvements.
Ensuring compliance with regulatory standards and quality requirements in the medical device field.
Supporting validation and verification (V V) processes for medical devices.
Requirements: Bachelors degree (B.Sc.) in Mechanical Engineering, Systems Engineering, or Electrical and Electronics Engineering (a Masters degree is an advantage).
At least 5 years of experience in the medical device industry.
Familiarity and experience working with multidisciplinary systems (mechanics, electronics, software).
Experience with regulatory standards and requirements in the medical device field (ISO 13485, FDA).
Strong technical skills and orientation for practical, hands-on work alongside management.
Proven leadership and management skills, including working in a dynamic environment.
Full proficiency in technical English.
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