Medical Supplier Quality Engineer

A leading life science and medical device manufacturing client in Hunt Valley, Maryland is looking to hire top talent to their quality engineering team! Serve as a highly visible Quality professional responsible for interpreting and applying Quality System requirements and developing, maintaining, and implementing Standard Operating Procedures (SOPs) and organizational policies within a regulated manufacturing environment. Support regulated diagnostic and/or medical-device products throughout the product life cycle, including manufacturing, distribution, and post-market activities. Lead major Quality System and business initiatives, including serving as a project manager and communicating project status to leadership. Provide expert guidance across core Quality System elements, including process control and supplier qualification, while identifying and driving continuous improvement opportunities. Apply statistical tools and data-analysis techniques to identify trends and root causes, drive corrective actions, and resolve moderately complex quality issues. Apply advanced quality engineering principles, technical concepts, and quality-science methodologies to deliver measurable and validated results. Provide training and mentorship to Quality team members and offer cross-functional guidance on Quality principles, policies, and best practices. Identify issues that could delay products or projects and recommend appropriate actions to mitigate risk and maintain timelines. Ensure documentation and quality processes comply with applicable regulatory and quality standards. Bachelor's degree with 10 years of experience in a regulated environment; At least 5 years of experience in Quality Engineering. Demonstrated success in root-cause determination and effective CAPA implementation. Ability to manage multiple priorities and lead successful, timely execution of complex projects. Experience leading or influencing Quality activities for engineering projects, including reliability engineering, validation planning and execution, and continuous improvement initiatives. Proficiency with statistical sampling, Six Sigma root-cause analysis methodologies, risk assessment, failure analysis, and project-management techniques. Working knowledge of applicable medical-device Quality System and regulatory requirements, including FDA 21 CFR Part 820 and ISO 13485:2016.Salary up to $120,000 annually + bonus