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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Based in the IT dept. will be a customer facing individual responsible for implementation and subsequent day to day support and maintenance of general Laboratory Computers systems in our QC, Chemistry, Micro and Process Sciences labs.
Supports the Downstream Manufacturing Support Process Sciences Department with analysis, troubleshooting, purification investigations and process validation of downstream manufacturing bioprocesses.
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.
Be responsible for managing internal/employee communications and external affairs including media relations, public affairs, and community engagement in support of Regeneron's Industrial Operations and Product Supply (IOPS) site in Limerick.
The Process Analytics IT Analyst will be responsible for the implementation and subsequent day to day support and administration of existing and future Business and Process Intelligence systems (currently Discoverant) in Raheen, Limerick.
This position in Regulatory Affairs involves the ability to integrate/apply knowledge of global regulations governing pharmaceutical drug development to all aspects of Regeneron's drug development programs. *
Implements policies and procedures to validate/qualify equipment, systems (inclusive of Continuing, CSV, Cleaning Val/SIP), and processes in accordance with regulatory requirements and company manufacturing standards.
The Manager of Supply Chain Systems and Analytics will be responsible for managing a mix of supply chain related projects that significantly impact the overall Supply Chain function and provide exposure to a wide range of individuals and functions.
Individual will develop, manage and lead the QAValidation Compliance team at Raheen, assisting with overseeing the realization of industry best practices while remaining adaptable to the changing needs of the company.
Responsible for overseeing information collection, distillation and assessment activities associated with the support functions and preparation of regulatory submissions and Product Quality Reviews, as required.