You need:Your BA/BS Engineering-oriented degree and 2+ years of experience in the medical device manufacturing supplier controls, or 4+ years of experience in the medical device manufacturing supplier controlsASQ Certified Quality Engineer, preferredCertified Auditor, preferredAuditing experience is required, preferably in the area of supplier auditsUnderstanding of and ability to interpret and apply ISO 13485, ISO 14971, and 21 CFR Part 820, specifically design controls, purchasing controls, risk management and production and process controlsProficiency leading CAPA investigations and supplier corrective actionStrong interpersonal relationship skills including negotiating and relationship managementStrong proficiency using MS Office Suite (e.g., Word, Excel, PowerPoint)Excellent written and verbal communication skillsAbility to work as a collaborative team member as well as independentlyExcellent attention to detail, producing high quality outputResults-oriented with appropriate urgency and tenacious follow-upFlexibility and strong organizational skills with ability to prioritize multiple tasksSound judgment when making decisions and communicating with internal and external customersWe offer:Competitive compensation including bonus and equityOpportunities for career advancementFull benefits packageAn evolving, engaging culture and workplaceNominated by our employees as a Top Place to Work in Orange County! Job Description Job Description Salary: $110,000 DOEOrthAlign, Inc., a Smart Technology, growing medical device company, has an immediate opening for aSupplier Quality Engineerresponsible for managing supplier programs for manufacturing, packaging, and other operational processes, as well as ensuring that quality programs are in compliance with regulatory requirements.