
Associate Director - QA - Medical Device Complaints
- Indianapolis, IN
- $118,500-173,800 per year
- Permanent
- Full-time
- Lead, mentor, coach and provide feedback to employees including participation in organizational planning, HR activities, financial management, and diversity objectives
- Review and approve complaint investigations associated with use, design, and manufacturing investigations for medical devices and drug/device combination products
- Maintain key product and process metrics reporting the performance of the quality system to management with executive responsibility and ensure timely escalations when necessary
- Drive product and process improvements using Root Cause Investigations, Complaint Actions, Trends, and Review Management
- Network within and outside of Lilly device organization to identify and implement opportunities for improvement and/or transfer of complaint handling Best Practices
- Review / write / approve GMP documents including technical reports, deviations/observations, procedures, and work instructions
- Collaborate and provide customer service for groups across Lilly. Share technical and complaint process knowledge and support investigations as needed.
- Support projects as part of cross functional Lilly teams
- Ensure that adequately trained personnel and approved procedures and resources are available locally and used for the completion of complaint investigations
- Support complaint related activities associated with new product launches
- Support device development processes by providing complaint analyses of predicate products as design input and by supporting complaint handling activities for clinical trials.
- Assist with and respond to internal and external audits/inspections
- Bachelor’s degree in Engineering, Medical or Life Sciences
- 5+ years of industry experience in areas including Quality, Technical Services, Research and Development or Manufacturing/Packaging.
- Experiences with Complaint processes, IT tools, and reporting
- Technical knowledge in design, manufacturing or validation; preferably devices
- Technical knowledge of complaint handling and quality systems; preferably devices performance
- Regulatory inspection experience
- Knowledge of regulatory requirements (e.g., cGMP, 21 CFR 820, ISO13485, applicable regulations for Canada, US, Australia, Brazil and Japan)
- Experience partnering with external parties/supplier/consultants
- Experience with Six Sigma methodology, e.g., participation on Six Sigma projects
- preferably experience working with medical devices
- Leadership ability and experience with multi-functional teams
- Excellent oral and written communication
- Basic knowledge in statistics and its applications
- Ability to compile data and metrics in reports understandable by management and business partners
- Strong computer literacy in Microsoft applications
- Attention to detail; self-management; problem solving; mentoring