Design & development of mechanical and electromechanical components & systems in the medical device domain.

Working on multiple projects simultaneously in product engineering such as gap assessments, design changes, manufacturing transfers, product development, regulatory or business-driven projects, etc.

Derive or remediate design requirements/engineering specifications (including performance, reliability, etc.) that meet the user need requirements.

Creation or remediation of Design History Files, Device Master Records and other related technical documents including drawings, labelling, packaging, instruction for use, etc.

Driving the engineering changes through proper planning & analysis of change impact, creation of change orders/notices & applicable documents, execution of change for implementation th...