Job description
QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields. Log on now to our website http://www. qrcgroup.com / to learn more about our services and solutions! We are seeking a Quality Associat e to support and maintain quality systems, ensuring compliance with GMP regulations, industry standards, and company policies within a regulated manufacturing environment.
The successful candidate will be responsible for reviewing and managing quality documentation, participating in investigations and corrective and preventive actions (CAPAs), providing quality support to manufacturing operations, and helping ensure that products, processes, and systems consistently meet established quality and regulatory requirements.
This role requires strong attention to detail, a commitment to continuous improvement, and the ability to collaborate effectively with cross-functional teams to drive quality excellence and operational compliance. 3 to 5 years of experience in process quality areas. Experience in regulated manufacturing environments. Knowledge of GMP documentation.
Experience with quality systems, investigations, documentation, and support of manufacturing processes. Bilingual (English & Spanish). All your information will be kept confidential according to EEO guidelines.