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:
Knowledge of GMP regulations and compliance requirements in a regulated pharmaceutical or medical device environment.
Experience operating, maintaining, and troubleshooting autoclaves and glasswashers.
Proficiency in Maximo CMMS software for work order management, preventive maintenance, and maintenance documentation.
Ability to prepare, review, and maintain technical documentation and maintenance records in compliance with GMP requirements.
Knowledge of Lockout/Tagout (LOTO) procedures and equipment safety practices.
Ability to troubleshoot equipment issues, identify root causes, and implement corrective actions.
Ability to read and interpret technical manuals, equipment specifications, and maintenance procedures.
Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.