Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron markets medicines for eye diseases, colorectal cancer, and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including hypercholesterolemia, oncology, rheumatoid arthritis, allergic asthma, and atopic dermatitis.
In Ireland, Regeneron have a corporate office based in Harcourt Street, Dublin and are currently building a world-class biopharmaceutical production facility in the Raheen Business Park, Limerick.
This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regeneron’s unwavering commitment to turn science into medicine.
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Regeneron is an innovative US multinational biopharmaceutical company. We are actively searching for an experienced regulatory professional to join our team on a 12-month basis. Location: Dublin or London
Summary: Responsible for the implementation and day to day operation of the Regeneron Manufacturing Execution System, the integrity of the data within the system and those provided by the associated data exchanges.
The Tech Transfer Manager, Compliance is responsible for ensuring adherence to regulatory guidelines and filings during the process transfer and transition to commercial operations for biological drug substance production.
The Process Engineer will work with the Manufacturing Sciences and Technology (MSAT) group in Rensselaer, New York to ensure site to site consistency after processes are transferred in Raheen.
Summary: This position receives, moves, and documents inventory and non-inventory items within the plant and from outside sources. This position also performs shipping functions as needed and raw material and dispensing functions.