We are a leading mRNA therapeutics company developing a new class of potentially transformative medicines to treat diseases caused by protein or gene dysfunction. Using our proprietary mRNA therapeutic platform (MRTTM), we create mRNA that encodes functional proteins. Our mRNA is delivered to the target cell where the cell’s own machinery recognizes it and translates it, restoring or augmenting protein function to treat or prevent disease.
The Quality Documentation Specialist is responsible for helping manage our Quality Management System and overseeing GxP documentation for Translate Bio, our contract organization resources, and our pharmaceutical/biotech partners. This person will participate in ensuring proper Quality and Compliance oversight for process development, manufacturing and nonclinical, clinical and commercial processes and supply chains.
Required Skills & Qualifications
Translate Bio is committed to equal employment opportunity. All applicants must have authorization to work in the U.S.