QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team.

In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.

Responsibilities:  Leads end-to-end execution of packaging and labeling changes required for EU MDR (European Medical Device Regulation) compliance.

Accountable for ensuring on-time delivery, cross-functional execution, and strong Business Unit alignment while managing packaging updates such as IFUs, cartons, and labeling changes.

Ensures all changes are implemented compliantly with no disruption to manufacturing or supply.