A unique opportunity to lead the lifecycle management of electronic systems for advanced medical devicesensuring regulatory compliance and delivering safe, high-quality products.
Key Responsibilities (Short Clear):
Prepare and review engineering documents, reports, specifications, and technical justifications in English.
Ensure proper use of system engineering, design controls, V V, and lifecycle processes.
Work closely with QA /RA teams to support audits, submissions, and documentation.
Collaborate with R D, manufacturing, quality, supply chain, and product teams for efficient development.
Participate in roadmaps, feasibility studies, and risk management.
Support design transfer, supplier evaluations, and sustaining engineering.
Communicate effectively with internal teams, partners, and regulatory bodies.
Bachelors or Masters degree in Electrical Engineering, Biomedical Engineering, Systems Engineering, or related field.
Minimum 10 years of engineering management experience, specifically in electronic systems development.
Proven experience in the medical device industry.
Deep understanding of medical device standards and design control requirements.
Strong command of English (reading, writing, and technical documentation).
