Provision of scientific and technical leadership to multidisciplinary teams to achieve corporate goals in challenging research projects within early-stage biologics drug development. Developing, executing and optimizing protein production processes
The role leads the site's independent Quality Assurance organization, accountable for an effective, risk based Quality system. The role is responsible for inspection performance/readiness activities, data integrity and accountable to ensure final batch
A key focus area of the position is the preparation of regulatory CMC documentation for small molecule products during development and commercial stage, in a manner that is scientifically sound, commercially viable and in accordance with current