We're sorry, the job you are looking for at Evotec on EuroPharmaJobs has expired.
Click here to see more jobs at Evotec .
We still have many live jobs. Click below for similar jobs in:
or go to our job search page.
You'll be the primary regulatory CMC voice on cross-functional matrix teams, covering everything from early clinical trial applications through to new marketing authorizations, post-approval changes, and full lifecycle management. That means you won't
Provide technical leadership and strategic guidance for upstream/downstream processing activities across the manufacturing network; Act as the primary point of contact for external partners, ensuring alignment with organizational goals; Lead harmonization
Design and execute experimental studies to develop and optimise purification processes for biologics; Evaluate and implement advanced chromatography and filtration technologies for intensified downstream processing; Develop scalable purification
Manage day-to-day QC lab operations, including raw materials, in-process, and final product testing; Lead analytical method qualification, validation, and transfer; Oversee analytical methods including flow cytometry, qPCR/ddPCR, and cell-based assays;
Drive continuous improvement initiatives, monitor quality performance metrics and identify opportunities to improve processes and team effectiveness. Ensure quality activities, including batch record review, quality event management and documentation, are