VP of Quality Assurance The VP of Quality Assurance (VP QA) is a key executive leader responsible for building, scaling, and overseeing SABs global Quality Assurance organization as the company advances from late-stage clinical development toward
Quality Assurance Manager The Quality Assurance Manager is a key member of SAB Biotherapeutics Quality Assurance function and is responsible for supporting and maintaining an inspection-ready Quality Management System across SABs biologics, clinical, laboratory, and GMP
Executive Director, Pharmacovigilance (PV) The Executive Director, Pharmacovigilance (PV) is a senior individual contributor and team leader who will serve as a cornerstone of the companys global drug safety function. This role has end-to-end accountability for
Quality Management System (QMS) Specialist The Quality Management System (QMS) Specialist is responsible for the administration, maintenance, and continuous improvement of the companys Quality Management System to ensure compliance with current Good Manufacturing Practices (cGMP) and
Vice-President Regulatory Affairs The Vice-President Regulatory Affairs is responsible for ensuring that compliance is being upheld for Regulatory Affairs at SAB Biotherapeutics (SAB). This role will lead preparation, review and submission of documents to FDA and
The Sr. Director, Medical Writing – Biologics will provide strategic and operational leadership for the preparation, development, and delivery of high-quality regulatory and clinical documents supporting the late-stage development and anticipated commercialization of SAB’s lead biologic