Validation Technician

The specialist will be part of a team responsible for production equipment, process and equipment validation (e. Process Validation), as well as providing extensive assistance with quality matters. The job includes collecting and analyzing data, writing reports, updating and maintaining processes, and monitoring relevant standards and regulations. Coordination with multidisciplinary teams on diverse projects is necessary. The workplace is at Kerecis' office in Ísafjörður and the job reports to the Prototyping & Manufacturing Development Manager. The Validation Technician supports all Process Validation efforts in ensuring the quality, safety, and compliance of medical devices by assisting with validation and qualification activities. This role involves executing validation protocols, collecting and analyzing data, and maintaining documentation. The technician works closely with cross-functional teams to support validation efforts for processes, equipment, and systems, ensuring compliance with regulatory standards. The Validation Technician is based in Kerecis offices in Ísafjörður and reports to the Prototyping & Manufacturing Development Manager.