Role DescriptionThe QA Manage will be responsible for ensuring that clinical processes are conducted in accordance with Guidelines, Directives, Regulations and applicable inter[national] laws.
ResponsibilitiesPerform Audits in internal, domestic and international sites within sites and vendors. Review and approve applicable controlled documentation Develop training material and train personnel on GCP related topics Manage and Provide guidance on GCP related aspects of clinical trials where appropriate. Generation and execution of QMS related procedures
Requirements5+ years experience in clinical trials working in a GCP regulated environment specializing in international biopharmaceutical [ATMPs] Preferably 3-5 years experience as an auditor BSc. in a relevant field An understanding of pharmaceutical manufacturing and GMP requirements Fluency in English and preferably Dutch
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Greg Silberstein.