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.

+ 1. Project Execution & Timeline Management

+ Lead full lifecycle project management for EU MDR packaging and labeling changes

+ Develop and maintain integrated project plans, i...