QC Quality Records Specialist III

The QC Quality Records Specialist III will act as a technical writer and be responsible for the overall management of quality records (deviations, change controls, investigations, CAPA, etc.) and generating GMP protocols/reports within Quality Control. This will include, but is not limited to, initiating quality records within Ascends quality management system (QMS), authoring and ensuring timely completion of the records and assisting in generation of protocol/reports to support GMP studies. Additionally, the incumbent will have the opportunity to interact with cross functional stake holders and 3rd party vendors. This role will report to the Director of Quality Control or designee.

Ascend is pioneering the future of healthcare through relentless innovation, our forward-thinking company is on a mission to manufacture safe, efficacious, and scalable gene therapies. Our vision is to set a new standard for gene therapy manufacturing through continuous scientific and...