SAB Biotherapeutics, Inc. seeks a seasoned Vice President Regulatory Affairs to lead all regulatory strategy and submissions for biologics development. The role requires directing cross-functional teams in FDA interactions, IND/BLAs/MAAs, and ensuring compliance across development and manufacturing.
VP Of QA The VP of 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 commercialization. Reporting to the
Director, Medical Writing Biologics The 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 SABs
Vice President Regulatory Affairs The Vice President Regulatory Affairs (RA) 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
VP Manufacturing The VP Manufacturing will provide strategic, operational, and technical leadership for the companys manufacturing activities supporting late-stage clinical development, commercial readiness, and future commercial supply of the companys lead biologic programs, including SAB?142. This
The Vice President Regulatory Affairs (RA) 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 ex-US
