Engineering And Quality Professional

Company Description Viant Medical is a global design and manufacturing services provider for the medtech industry, specializing in areas such as surgical technologies, orthopedics, cardiac & interventional, bioelectronics, and drug delivery. Offering end-to-end capabilities from design and development to manufacturing and packaging, we help bring life-impacting medical devices to market. Rooted in the Latin word for “life,” our mission is to enhance patient care through innovative medical technology solutions. With 25 global locations, over 6,000 employees, and extensive manufacturing resources, Viant combines small-company attention with big-company capabilities to serve diverse medtech markets. Role Description This is a full-time, on-site role based in Tijuana, BCN, for an Engineering and Quality Professional. The individual in this position will be responsible for ensuring product quality and process efficiency through the implementation of quality control systems, process validation, and compliance assessments. Duties include supporting continuous improvement initiatives, collaborating with cross-functional teams, conducting root cause analyses, and preparing documentation aligned with regulatory standards. The role requires a blend of technical expertise and problem-solving abilities to ensure operational excellence and customer satisfaction. Qualifications Knowledge of Quality Assurance, Quality Control, and regulatory compliance in the medtech or manufacturing sectorEngineering skills in process validation, design development, and equipment qualificationExperience with problem-solving methodologies such as Six Sigma, Root Cause Analysis, and Corrective Action PlanningProficient in data analysis, statistical techniques, and the use of tools such as Minitab or equivalentStrong project management, documentation, and organizational skillsExcellent communication skills to collaborate effectively in cross-functional teamsBachelor’s degree in Engineering, Quality Management, or a related field is requiredRelevant certifications such as Six Sigma, ISO Auditor, or ASQ Certification are beneficialWorking knowledge of medical device manufacturing standards (ISO 13485, FDA regulations) is an advantage