We are a worldwide leader in specialized diagnostics in Hemostasis, Acute Care Diagnostics, Autoimmunity and Transfusion and transplant. In addition, we research, develop, and manufacture customized assays and biomaterials through our OEM business line. As an integral part of Werfen, a global healthcare company dedicated to delivering the highest quality in vitro diagnostics products.
In Werfen, we are looking for a Quality Systems Engineer. She/he is responsible for ensuring the company is compliant with all applicable regulations and standards. Is autonomous regarding audit organization and capable of conducting audits, being part of the subject matter experts (SME) as well, especially for the QS&C responsibilities. Participates in the continuous improvement of the QRA area, being supportive in the Non-conformance, Change Control, and CAPA process enhancement and leads the documental management system of the company. Owns and manages the Change Control Management System.
Our Purpose: We contribute to the advancement of patient care around the world through innovative specialized diagnostics. JOIN US!