Specialist QA

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 Specialist QA with GMP manufacturing experience in Quality Assurance, including review and approval of change controls, deviations, CAPAs, protocols, reports, and procedures.

Experience supporting packaging/inspection operations, strong knowledge of GDP and electronic quality systems, and the ability to collaborate effectively with Manufacturing, Engineering, and Process Development are highly desired. Degree in a related field with applicable experience: Doctorate, Master's + 2 years of experience, Bachelor's + 4 years of experience, Associate's + 8 years of experience, High School Diploma/GED + 10 years of experience.

Bilingual English and Spanish communication skills. Experience in Quality Assurance within a GMP-regulated environment. Experience reviewing and approving Change Controls, Deviations, CAPAs, Protocols, Reports, and SOPs. Experience supporting packaging and inspection operations. All your information will be kept confidential according to EEO guidelines.