QA - IDM Device Complaints

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.Job Description:Support the Product Complaint Handling and Medical Device Reporting Processes. This role is designed for an individual who is curious, embraces new digital tools and ways of working, and helps drive practical change across complaint reporting, trending, and stakeholder support.Specific functions, duties, or tasks:Author/review/approve GMP documents including technical reports, deviations, change controls, inspection procedures, process level procedure, and work instructionsLead authoring and management of deliverables to support Global Patient Safety and device safety case reportingAuthor regulatory responses and represent Indianapolis Device Manufacturing (IDM) at inspections/auditsAct as Data Steward for complaint data and ad hoc queries and special issuesBusiness owner/SME for new device complaints related systemsMaintain trend analysis on product and process performanceConduct vigilance trending to support potential trend reportingProduce and document periodic metrics/ad-hoc reports on process and product performance.Collaborate and provide customer service for groups external to IDM, including, but not limited to, manufacturing sites, OUS Affiliates, Global Patient Safety, US Complaint Management, Third Party Manufacturers, Material Suppliers and call centersRepresent IDM complaints group at cross-functional Device Surveillance activitiesSupport continuous improvement projectsOwn, coordinate or participate in project work that requires substantial technical knowledge and continuous improvement skillsNetwork within and outside IDM to identify opportunities for improvement and/or transfer IDM best practices to business partnersMentor and coach less-experienced QA Representatives and Assistants, as applicablePerform notifications to management as requiredMinimum Experience/Qualification Requirements:Minimum of five years industry related experience in areas, which may include Quality, Technical Services, LRL Product Development, or Manufacturing Operations.Bachelor’s degree in Engineering, Medical or Life Sciences preferred.Technical knowledge in design, manufacturing and validation; preferably deviceTechnical knowledge of complaint handling and quality systems; preferably device performance and functionalityKnowledge of regulatory requirements (e.g., cGMP, 21 CFR 820, ISO13485, applicable regulations for Canada, US, Europe, Australia, Brazil and Japan)Experience with Third party / supplier / consultant interactionsExcellent oral and written communicationWorking knowledge of statistics and its applications; able to translate data into clear, actionable insights and drive discussion on trends and performance.Ability to compile, analyze, and visualize data and metrics into reports understandable by management and business partners; proactively identifies opportunities to standardize, simplify, and automate reporting where appropriate.Proficient with Microsoft 365 applications (e.g., Outlook, Word, Excel, PowerPoint).Attention to detail; Self-management; Problem solving; Team player; MentoringAdditional Preferences:Experience with Complaint Processes, IT Tools and Complaint ReportingPreferred tech skills: dashboarding/data visualization (e.g., Power BI/Tableau), advanced Excel, basic SQL or similar querying, and experience with electronic quality systems (e.g., TrackWise, Veeva)Experience with Six Sigma methodology, e.g., participation on Six Sigma team or project.Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization and/or visas for this role.Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women’s Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.Actual compensation will depend on a candidate’s education, experience, skills, and geographic location.  The anticipated wage for this position is$126,000 - $204,600Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medi