QA/RA Manager — GMP, FDA Submissions & Quality Systems

A leading biotechnology firm in Cambridge is seeking a full-time QA/RA Manager to oversee quality assurance and regulatory activities. This on-site role involves ensuring compliance with regulatory requirements, managing quality systems, conducting audits, and maintaining adherence to Good Manufacturing Practice (GMP). Experience in Quality Assurance principles and regulatory processes, preferably with FDA submissions, is required. The position offers an opportunity to contribute to the development of high-quality products in an innovative environment.#J-18808-Ljbffr…