JT371- SPECIALIST QA
Location
Juncos, PR
Job Type
Full-time
Category
other-general
Posted
June 19, 2026
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:
+ Perform quality disposition decisions (approval/rejection) for bulk drug substances in compliance with regulatory standards.
+ Provide Quality oversight to ensure that operations for clinical and licensed pharmaceutical Drug Substance (API) are manufactured, tested, stored, and managed according to current Good Manufacturing Practices (cGMP), Good Laboratory Practices (cGLP), and other applicable regulations.
+ Ensure all deviations are properly identified, investigated, documented, and resolved according to procedures.
+ Ensure that changes that could potentially impact drug substance quality are asse...
Responsibilities:
+ Perform quality disposition decisions (approval/rejection) for bulk drug substances in compliance with regulatory standards.
+ Provide Quality oversight to ensure that operations for clinical and licensed pharmaceutical Drug Substance (API) are manufactured, tested, stored, and managed according to current Good Manufacturing Practices (cGMP), Good Laboratory Practices (cGLP), and other applicable regulations.
+ Ensure all deviations are properly identified, investigated, documented, and resolved according to procedures.
+ Ensure that changes that could potentially impact drug substance quality are asse...