QCLabTechnician

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. **Organization Overview:** Indianapolis Device Manufacturing (IDM) is responsible for the development, commercialization, manufacture, and global technical stewardship of delivery devices used to administer many of the therapeutics in Lilly's portfolio. This includes the development and delivery of test systems and test methods in support of design verification, production, and complaint handling. **Responsibilities:** The QC Lab Technician, Device Quality, is primarily responsible for providing technical support and expertise for work processes and activities associated with laboratory operations, performing testing in support of commercial and development product, and supporting laboratory investigations. * Develop and maintain knowledge of applicable regulations, LQS, and GQS requirements in order to network and influence Lilly’s and the industry’s application. * Implement, maintain, and/or enhance appropriate quality systems within IDM QC laboratory. * Provide Quality Control support for the IDM QC laboratory. * Author, maintain, and instruct on OJT courses for laboratory equipment, testing inspection, and laboratory operations. * Perform and oversee QC laboratory equipment setup, operation, and maintenance. * Build and maintain working relationships with DDR&D, TS/MS, Lilly final Device Assembly/ Packaging Sites, and Contract Manufacturers supporting batch release testing of Lilly product. * Participate in new product des