We are looking for a qualified Validation Specialist with experience in GMP-regulated environments and pharmaceutical processes. Requirements 3 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)
QRC group is a life science firm dedicated to provide services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields.
Our services and solutions include:
Process and Laboratory Investigation
• Corrective and Preventive Action (CAPA)
• Change Control
• Training
• Document Management Control
• QA Laboratory
• Methodology Transfer and Validation
• Instrument Calibration
• Validation and Training in Chromatographic Data Acquisition System
• Cleaning Validation
• Automation Engineering
• Quality Systems
