Description

Manage design and documentation processes for medical device projects, ensuring compliance with industry standards across all project phases.

This role is on-site.

Responsibilities

• Execute design input, output, and verification deliverables for new product development and sustaining projects.
• Manage technical documentation for remediation and new product initiatives.
• Navigate designs through project phases using standard documentation practices.
• Apply industry practices to new technologies with minimal supervision.
• Handle ECO/ECN routing and maintain strong verbal and written communication.

Required Skills

• 4-7 years of experience in the medical device industry.
• Bachelor’s Degree in Mechanical Engineering or an equivalent engineering degree.
• Proficiency in CAD tools, specifically SolidWorks or Creo.
• Experience with PLM tools.
• Strong understanding of Good Documentation Practices (GDP).
• Experience in design, manufacturing, or testing within the medical industry.
• Competency in ECO/ECN routing.

Preferred Skills

• Exposure to EUMDR or other regulatory requirements.

Key Skills

Education

ANY GRADUATE