Position Overview:

We are seeking a driven and hands-on R&D Engineering Co-op to support our R&D team in the development, testing, and improvement of medical device reprocessing solutions. The ideal candidate will be passionate about engineering and healthcare innovation, with a strong willingness to learn and contribute to a variety of tasks within a fast-paced, small team environment. This co-op position offers a unique opportunity to gain real-world experience in medical device engineering and reprocessing technologies.

Key Responsibilities:

Assist in the design, prototyping, and testing of new medical device reprocessing solutions. Support the team with data analysis and interpretation of testing results. Participate in design verification and validation activities to ensure compliance with regulatory standards. Conduct material testing, process optimization, and other hands-on engineering tasks. Collaborate with cross-functional teams (including regulatory, quality, and operations) to meet project milestones and deliverables. Assist with the documentation of development processes, testing protocols, and results. Provide recommendations for improvements in product design, reprocessing techniques, or workflows based on findings. Stay current on industry trends, best practices, and regulations related to medical devices and reprocessing. Assist with process improvement initiatives to streamline existing processes

Required Qualifications:

Currently enrolled in a Bachelor's or Master's degree program in Mechanical Engineering, Biomedical Engineering, Electrical Engineering, Chemical Engineering, or a related field. Strong academic background with coursework or experience in product design, prototyping, and testing. Hands-on experience with laboratory equipment, materials testing, or engineering tools. Knowledge of engineering principles and problem-solving techniques. Strong communication and teamwork skills. Detail-oriented with the ability to manage multiple tasks and meet deadlines. Interest in the healthcare and medical device industry.

Preferred Qualifications:

Previous internship or co-op experience in medical device engineering or a related field. Familiarity with FDA regulations (21 CFR 820) or other medical device standards. Proficiency in CAD software (SolidWorks, AutoCAD, etc.). Preferred minimum GPA of 3.5 demonstrating excellence in the ability to learn and retain information

Benefits:

Gain valuable, hands-on experience in medical device engineering. Opportunity to work in a growing company with a dynamic, innovative team. Mentorship and professional development opportunities. Competitive compensation.