Denmark Contract Manufacturing
FDF manufacturing site
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Xellia Pharmaceuticals has become aware of recruitment scams where fraudulent company representatives are contacting individuals and unauthorized appear to act on behalf of Xellia to offer fake job opportunities. Please note that Xellia’s use of recruitment companies to reach out to potential candidates never involves requests or authorises payment of any kind to process job applications or downloading of software.
If you have been contacted by anyone representing themselves as being from Xellia or on behalf of Xellia and are concerned about their legitimacy, please note that all actual open job positions at Xellia will be shown on our own website, here
If you have experienced any of these recruitment scams, please report to your local authorities. You can find more information on scams, as well as how to report a scam for the United States at https://www.consumer.ftc.gov/articles/0243-job-scams
Xellia Copenhagen offers contract manufacturing services for lyophilized products and products requiring aseptic fill capabilities. The Copenhagen site operates alongside Xellia’s other manufacturing plants in Cleveland, USA; Budapest, Hungary; and Taizhou, China as well as our centralized laboratory service in Budapest, as part of its vertical integration strategy.
This site’s production capacity is currently used to produce Xellia's own product pipeline for various customers and will be used for further opportunities for CMO services.
Xellia Pharmaceuticals’ aseptic filling line has an excellent compliance track record with a history of successful inspections by authorities worldwide.Learn about our capabilities
We are continuously looking to partner and expand our capabilities based on your needs and we can offer individualized and innovative solutions.
Our highly skilled cross-functional team is dedicated to working with our partners to manufacture and supply their products. Our support can be tailor made to our partners' needs ranging from full R&D support, to regulatory approval, launch, commercial production and Medical Affairs support.