Oxford Global Resources offers a unique and excellent opportunity to work as a QA Auditor GxP delivering services to global animal health company dedicated to deliver quality medicines and vaccines, complemented by diagnostic products and genetic tests.
Job Description
As a contract member you will work within Regulatory Affairs, Global Quality & Compliance group, providing on request quality assurance support for the Veterinary Medicine Research & Development (VMRD) clinical and non-clinical programs.
Responsibilities
- perform quality assurance audits of clinical and non-clinical veterinary product studies and reports with limited supervision. Audit types may include: protocols, investigator study sites, data & data listings, summary & analysis, final study reports, master study files, facility & processes, contract research organizations and pharmacovigilance systems.
Requirements
- This is a full-time job with a long term contract; home-based is an option but travelling outside Barcelona might be needed from time to time to attend on-site meetings. English is mandatory as this is an international project.
- Previous experience working in GxP (GLPs/GCPs/GPVs) mandatory.
Should you consider any new challenges as a professional either as an employee or as a freelancer please do not hesitate to send your CV and contact details. Should you know anyone who may match the role, please do not hesitate to forward this email and contact details.
