Description

You will support the design and manufacturing processes for handheld medical devices, ensuring compliance with regulatory standards.

Responsibilities

• Apply design and manufacturing processes specifically for handheld medical devices.
• Ensure all engineering activities comply with medical device regulatory standards.
• Maintain technical documentation and communication regarding device development.

Required Skills

• Bachelor’s degree in Electrical Engineering.
• 5+ years of professional work experience (internships and academic projects excluded).
• Direct experience with Medical Device regulatory requirements.
• Working knowledge of cGMP, FDA, and ISO13485 standards.
• Understanding of medical device design and manufacturing workflows.
• Strong written and verbal communication skills.

Key Skills

Education

Any Graduate