Senior Manager, Quality Assurance at Enovis in Fort Worth, TX

Job description

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 pay attention to the details. We embrace collaboration with our partners and patients, and take pride in the pursuit 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. Why work at Enovis? See for yourself . 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 : Sr Manager, Quality Assurance Reports To : Director, Quality Assurance Location: Fort Worth, TX Business Unit Description : QA Job Title/High-Level Position Summary: The Sr. Quality Assurance Manager is responsible for leading a team of quality engineers and Quality technicians in driving product and process excellence across the Recovery Sciences /Bracing and Support device portfolio. This role ensures compliance with regulatory standards, support manufacturing as well as new product introduction and fosters a culture of continuous improvement. The Sr. Quality Assurance Manager will collaborate cross-functionally to implement quality strategies that enhance product reliability, reduce risk, and improve operational efficiency across multiple locations. Key Responsibilities : Lead and mentor a team of quality engineers and technicians, providing technical guidance and performance management. Develop and implement quality strategies that align with business objectives and regulatory requirements. Lead quality engineering support for manufacturing operations, ensuring robust process controls, effective risk management, and validation of production methods. Ensure compliance with FDA QSR (21 CFR Part 820), ISO 13485, and ISO 14971 standards. Drive root cause analysis and corrective/preventive actions (CAPA) for product and process issues. Collaborate with Manufacturing, R&D, Regulatory Affairs, and Supply Chain to resolve quality challenges and improve processes. Support internal and external audits, acting as a subject matter expert for quality engineering practices. Maintain and improve quality system documentation, including procedures, work instructions, and validation protocols. Be qualified as a Laser safety officer for the DFW location. Represent the LiteCure, TJM, and TJD Quality Management System as Management Representative. Travel requirements: 50% to Tijuana sites Minimum Qualifications Bachelor’s degree in Engineering (Mechanical, Biomedical, Industrial, or related field); Master’s degree preferred. 8+ years of experience in quality engineering within medical devices or other regulated industries, including 3+ years in a leadership role. Strong knowledge of ISO 13485, FDA QSR, ISO 14971. Proven ability to lead cross-functional teams and manage complex projects. Excellent communication, analytical, and problem-solving skills. Desired Characteristics: ASQ Certified Quality Engineer (CQE) or Certified Quality Manager (CQM), Certified Quality Auditor (CQA), or Six Sigma Black Belt. Familiarity with eQMS systems, statistical software, and metrology tools. Demonstrated success in driving quality improvements and regulatory compliance. Currently, Enovis does not provide sponsorship for employment visas (e.g., H-1B) and will not offer such sponsorship in the future. Applicants must already have full-time work auth