About Us
For over two decades, our commitment to pioneering approaches has led to numerous breakthroughs, significantly improving the lives of those affected by rare genetic diseases. In 1997, we were founded with a singular goal: to make a meaningful difference in small patient populations. We are now poised to amplify this impact by applying the same science-driven, patient-centric approach that has driven our last 25 years of drug development to larger genetic disorders, as well as genetic subsets of more common conditions.
Through our unparalleled expertise in genetics and molecular biology, we will continue to develop targeted therapies that address the root cause of the conditions we seek to treat. Our unwavering dedication is not just a calling, but an obligation to those who will benefit most. The ultimate objective has always been to improve lives, and now we can reach more.
Our Technical Operations Group
BioMarin's Technical Operations group is responsible for creating our drugs for use in clinical trials and scaling production for the commercial market. This team consists of engineers, technicians, scientists, and support staff who build and maintain BioMarin's cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure regulatory standards are met, and procure necessary goods and services to support manufacturing and coordinate the worldwide movement of our drugs to patients.
Manufacturing Apprentice Opportunity
This 2-year program combines on-site workplace learning at BioMarin in Shanbally, Ringaskiddy, with academic studies at Munster Technological University (MTU), leading to a Level 6 Higher Certificate of Engineering in Manufacturing Engineering. As a Manufacturing Apprentice, you will be part of the BioMarin Drug Substance Manufacturing team, working in a fast-paced, collaborative, and supportive environment where learning, growth, and development are endless.
Responsibilities
* Develop knowledge of GMP standards and equipment operation.
* Learn manufacturing best practices and develop skills required to manufacture high-quality drug substance in accordance with GMP and safety requirements.
* Provide support to on-site drug substance manufacturing personnel in daily routine and non-routine tasks.
* Perform all aspects of biologic manufacturing, including cell culture growth, harvest, filtration product capture, chromatography, ultra-filtration, raw material dispensing, media and buffer preparation, filling, and preparation of product for transportation.
* Support continuous monitoring and control of cell culture and purification processes, including in-process sampling and testing per approved procedures.
* Assist with investigation and resolution of process investigations.
* Participate in writing, review, and revision of manufacturing documentation as necessary.
* Earn while you learn.
* Annual bonus.
* Onsite gym.
* Free car parking.
* Subsidised canteen.
Requirements
* Achieved at least Grade 06 in 5 Leaving Certificate subjects, including Mathematics, English, and preferably one Technical / Science subject with a minimum of 250 CAO points.
* Applications also open to those completing their Leaving Certificate in June 2025.