Job Description
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: Ensures all work is completed with minimal disruption and in compliance with all cGMP guidelines and client's procedures.
Direct and coordinate daily activities of personnel responsible for material receipt, storage and transport.
Ensures materials are received, stored and transported according to established performance standards and all applicable procedures and regulations.
Interacts with internal and external regulatory agencies to ensure compliance with cGMP, DOT, OSHA requirements.
Collaborate with other sites to maintain optimal flexibility for the storage of all ma...
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