JT078 - SPECIALIST QA

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: Review, approve, and maintain manufacturing process documentation (MPs) in compliance with cGMP requirements Review, approve, and ensure accuracy, completeness, and traceability of GMP documentation , including protocols, reports, investigations, and quality records Approve process validation protocols and reports , including PPQs and cleaning validation documentation Participate as Quality representative on incident triage teams, ensuring timely and compliant decision-making Review and approve planned incidents, deviations, and nonconformances , ensuring appropriate risk assessment and documentation Approve Env...