Description

The Device Engineering team at Gilead is seeking a qualified individual to support drug device combination products throughout the commercial lifecycle. This individual will be responsible for the management of combination product change records. Additional responsibilities include test sample management, post market surveillance reports, and risk management file maintenance.



Job Responsibilities

Coordinate and manage combination product change control records

Initiate, route, and close change records for product and manufacturing process changes.

Initiate, route, and close change records for the design and development of drug device combination products, including the creation and management of design control documentation.

Coordinate and manage test sample builds

Manage sample requests and procurement.

Coordinate test sample delivery logistics.