<p>Come join a growing, steady company! Excellent Benefits and a great team to work with.</p> <ul> <li>Full Medical, Dental & Vision, 401(k), effective on your 1st day </li><li>Generous paid time off benefits and 10 paid Holidays </li><li>Growth Opportunities </li><li>Earn additional ($800) for Monthly Attendance Bonus </li><li>On-Demand Pay: Access your pay as soon as you have earned it! </li></ul> <p>This is a unique role where you will have the opportunity to work as part of the quality assurance team supporting document control and quality control.</p> <p>PURPOSE: As a member of the Quality Assurance team this position will support aspects of the Quality department related to inspection of product and documentation control in accordance with all Standard Operating Procedures, GMP's, company policies and procedures, and appropriate agency requirements governing the manufacture of medical device products.</p> <p>INNOVATION: At Viant our associates' safety is #1. A safe workplace creates and maintains an environment where our associates can feel confident and safe coming to work every day. Innovation is key to our success and growth and we are excited to have the latest technologies our associates can use!</p> <p>GROWTH: Being a growth site we are looking for individuals that are looking for development.</p> <p>MISSION: We partner and innovate with our customers to provide the highest quality, life enhancing medical devices in the world.</p> <p>Skills/Competencies</p> <ul> <li>Providing support to document control </li><li>Providing support for internal and external audits </li><li>Uses standard measuring tools, measuring machines, and electronic instruments to perform inspections in accordance with authorized specification and quality control standards. </li><li>Inspect vendor supplied components/assemblies </li><li>Calibration support, to assist the Calibration Technician as-needed </li><li>Prepares necessary documentation and ensures paperwork compliance on all inspected items, including filing, scanning and verification of device history records. </li></ul> <p>Requirements:</p> <ul> <li>Minimum Education: High school diploma preferred </li><li>Minimum Experience: 2 years' experience in manufacturing industry, preferably within the medical device industry; with quality management systems experience a plus </li><li>Knowledge & Skills: </li><li>Proficient in computer applications such as, Microsoft Word, Excel, Access and Outlook </li><li>Understanding of office procedures, including filing, record management and archiving documentation </li><li>Experience with inspection tools including mechanical, CMM and other computer assisted systems </li><li>Ability to understand part drawings/blueprints, GD&T knowledge </li><li>Strong analytical and problem solving skills </li><li>Ability to multi-task </li><li>Proactive, demonstrates initiative and self-motivated </li><li>Strong communication and organizational skills </li><li>Ability to work autonomously or in a team environment </li><li>Detail oriented </li></ul>