Quality & Reliability Engineering Supervisor

About the role

As a Quality & Reliability Engineering Supervisor at TE, you will lead the development and maintenance of world‑class quality processes for medical device manufacturing. You will work closely with site quality leaders, project teams, and customers to ensure product quality and regulatory compliance.

Key responsibilities

• Develop, implement, and continuously improve the site Quality Management System (QMS) in line with ISO 13485 and FDA requirements.
• Plan, conduct, and report on internal audits, management reviews, and supplier assessments.
• Represent the Global Quality organization in customer meetings and business reviews.
• Coordinate with the Project Management Office on new product introductions and site transfers that impact the QMS.
• Support electronic quality system implementation and act as quality approver on engineering change orders and related documentation.

Required profile

• Proven experience in process compliance, auditing, and quality system management.
• Strong problem‑solving, research, and report‑writing abilities.
• Excellent communication and interpersonal skills with the ability to prioritize tasks.
• Ability to work independently and lead initiatives across multiple sites.

Required skills

• ISO 13485
• FDA quality requirements
• Lead Auditor certification
• Internal audit execution
• Quality Management System (QMS) knowledge