Medical Device Design Quality Engineer

Who We Are ABOUT ENOVIS™ Enovis Corporation (NYSE: ENOV) is an innovation-driven medical technology growth company dedicated to developing clinically differentiated solutions that generate measurably better patient outcomes and transform workflows. Powered by a culture of continuous improvement, global talent and innovation, the Company’s extensive range of products, services and integrated technologies fuels active lifestyles in orthopedics and beyond. For more information about Enovis, please visit www.enovis.com . What You'll Do At Enovis™ we sweat the little things. We embrace collaboration with our partners and patients, and we glory in the grind of scientific excellence — with the goal of transforming medical technology as we know it. Because that’s how we change the lives of patients for the better. And that’s how we create better together. As a key member of the Quality Assurance team you will play an integral part in helping Enovis drive the medical technology industry forward through transforming patient care and creating better patient outcomes. Job Title : Quality Assurance Engineer – Design Quality Focus Reports To : Design Quality Engineering Manager Location: Austin, TX Business Unit Description : US Surgical Job Title/High Level Position Summary : Utilizing a comprehensive knowledge of engineering and problem-solving principles, this position is responsible for a variety of complex activities regarding the design, implementation, and maintenance of quality assurance procedures and work instructions to ensure external safety, quality, and compliance with complex Company standards and government regulations. This position primarily supports New Product Development and Sustaining Product Development and serves as the QA representative on various PD initiatives. Key Responsibilities : Participating in design and manufacturing reviews Generating DFMEAs/UFMEAs and participating in risk analysis discussions Reviewing and approving design and development documentation Serve as subject matter expert for design quality in ISO and FDA audits Authoring procedures and work instructions that define and govern the quality system Conduct internal audits of the quality system and other business functions Evaluating nonconforming material and dispositioning based on cross-functional engineering review Assuring compliance to internal and external specifications and standards (i.e. GMP, ISO, FDA, MDD) Reviewing trends in device failures associated with customer complaints and nonconforming material Leading and owning corrective and preventive actions Participating in Health Hazard Evaluations Working on complex special projects as assigned Minimum Basic Qualifications : Bachelor’s in Biomedical or Mechanical Engineering and 3+ years of experience, with at least 1 year in design focused environment (or equivalent combination of education and years of experience). Background in Medical Device,…