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 looking for a qualified Validation Specialist with experience in GMP-regulated environments and pharmaceutical processes.
1 to 5 years of experience in a GMP environment. Experience in the pharmaceutical industry. Knowledge of and experience with aseptic and regulated processes. Experience developing and executing: Validation protocols. Validation reports. SOPs (Standard Operating Procedures). Statistical data analysis. Ability to work on multidisciplinary projects and comply with regulatory requirements.
Bilingual (English ans Spanish) All your information will be kept confidential according to EEO guidelines.