We're currently recruiting for an exciting opportunity with a biopharmaceutical organization based in Dunboyne.
This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.
Duties Collaborate with stakeholders to execute the transfer requirements of both late stage clinical and/or PPQ (Process Performance Qualification) programs.
Attend meetings with local and international groups to coordinate and execute implementation tasks for new Drug Substance processes.
Manage new program introduction schedule to ensure tasks are executed on schedule and right-first-time.
Collaborate with stakeholders to deliver GMP documents related to TT, such as Risk assessments, change controls, batch records, sampling plans, Bills of Material.
Support development of process descriptions, process models, facility fits, and other Tech Transfer-related documents for continuous and fed-batch processes Employ innovative and continuous improvement mindset to identify and implement opportunities to enable product launch.
Ensure the highest Quality, Compliance and Safety standards and embody Safe by Choice – know and follow the Safety, Health and Environment guidelines and work towards company safety and environmental goals Ability to solve problems and take new perspectives on existing solutions with a desire to continuously learn, improve and develop.
Excellent trouble shooting and problem-solving skills as well as influencing, collaboration skills and teamworking ability to work with global and interdisciplinary teams.
Education