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This role is focused on ensuring compliance with environmental, health, and safety regulations across their manufacturing operations. The role involves managing risk assessments, conducting safety audits, driving continuous improvement initiatives, and promoting a strong safety culture. Key responsibilities include developing and implementing safety policies, conducting training, and ensuring adherence to local, state, and federal regulations.
As the Quality Engineer you will gain hands on experience in medical device development, focusing on manual testing, design controls, sterilization, and transit testing. You will collaborate closely with mechanical engineers and cross functional teams to ensure compliance with FDA regulations and ISO 13485 standards.
The Product Development Quality Engineer ensures the highest quality standards for advanced micromanufactured components used in medical devices, focusing on compliance, process improvement, and defect prevention. The role involves collaborating with cross-functional teams to develop and validate robust quality systems, driving innovation in medical device manufacturing.
The ideal project engineer candidate will have 3-5 years of experience supporting construction projects-specifically mid-rise (6-story) and mixed-use developments. You'll play a key role in coordinating submittals, RFIs, and construction documents while working closely with seasoned project managers and superintendents.
The Manufacturing Engineer will sit on a small team reporting into the Manufacturing Engineering Manager. In this role you will get to work autonomously, wearing many hats, supporting the manufacturing of surgical medical devices.
The Manufacturing Engineer focuses on integrating new projects into production and enhancing existing manufacturing processes to improve efficiency, quality, and ergonomics. It requires strong technical problem-solving, the ability to manage projects independently, and occasional customer interaction to clarify technical requirements.
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