Intern - Manufacturing Engineer
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About The Position
The Manufacturing Engineer Intern will conduct engineering studies and validations for a broad range of technologies to provide new or improved manufacturing processes to the medical device market, specifically in the arena of Interventional Urology. This role is crucial as it supports the Operations team in fulfilling Coloplast's business goals for manufacturing projects. The intern will be involved in validating medical device manufacturing processes in accordance with applicable regulatory standards, ensuring that all processes meet the necessary compliance requirements. In addition to validation, the intern will identify cost-savings projects and process efficiency improvements while maintaining product quality. This involves implementing process improvements under the guidance of project engineers and scientists, conducting Design of Experiments (DOEs), and preparing process validation protocols and reports. The intern will also participate in hands-on problem-solving and resolution, working directly with mechanical and chemical process control systems. A key responsibility will be to create and maintain accurate records of lab work and test results related to assigned projects. Coloplast emphasizes the importance of conducting business to the highest ethical and professional standards, requiring compliance with applicable laws and regulations, as well as adherence to the Advamed Code of Ethics on Interactions with Healthcare Professionals and company policies.
