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.