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This application is for a 12-week internship role from June - August 2025. Resume review begins in February 2025. The Manufacturing Engineering group at Biogen plays a crucial role in advancing the production of bulk drug substance by ensuring the efficient operation of both upstream and downstream manufacturing processes. The team is responsible for managing and troubleshooting the complex systems involved in the manufacture of biopharmaceutical drug substance, ensuring that all equipment functions optimally in a Good Manufacturing Practice (GMP) environment. By focusing on equipment reliability and maintenance, the group directly supports the company's mission to deliver high-quality, safe, and effective therapeutic products to patients. Interns will gain hands-on experience in troubleshooting issues that arise with the bioprocessing systems and learn to interpret critical engineering documents, such as process and instrumentation diagrams (P&IDs) and equipment specifications. Additionally, they will navigate the company's engineering support systems, which are designed to enhance operational efficiency and ensure compliance with industry standards. By working with a skilled team, interns will contribute to the ongoing optimization of manufacturing processes, ensuring that the company's products meet stringent quality requirements. This role offers valuable insight into the critical aspects of bioprocessing that drive the company's mission of improving patient outcomes through innovation and excellence in manufacturing.
