Job Information
Lilly Complaints Investigator in Concord, North Carolina
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.
Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is
$96,000 - $140,800
Responsibilities:
Conduct investigations into manufacturing and packaging complaints for prefilled devices and combination products, conducting thorough trend analyses and preparing comprehensive reports. Collaborate with internal and external partners to drive continuous improvement initiatives while mentoring junior QA associates to enhance team capabilities.
Key Objectives/Deliverables:
Perform complaint investigations for Concord manufacturing and packaging complaints for prefilled devices and drug/device combination products, drug/device combination products, and parenteral products.
Support and initiate TW Trend, RCIs, Tasks or other technical investigations, as applicable
Perform quarterly trend analysis and investigations on product and process performance
Compile and document monthly metrics/quarterly metrics/ad-hoc reports
Understand the devices/combination products/parenteral packaging processes to support investigations
Collaborate and provide customer service for groups external to Concord
Support continuous improvement projects and new launches as applicable
Compile and present complaint data for Site Lead, Flow, and Process teams
Complete the eAPR complaints sections for each required product including compiling/summarizing data and presentation support as necessary
Mentor and coach other QA Associates, as applicable
Basic Qualifications:
Minimum of three years industry experience
Technical knowledge in design, manufacturing or validation; preferably devices
Technical knowledge of complaint handling and/or quality systems; preferably device packaging/assembly
Knowledge of regulatory requirements (e.g., cGMP, 21 CFR 820, ISO 13485, international standards)
Strong computer literacy in MS Office
Additional Preferences:
Basic knowledge in statistics and its applications
Ability to compile data and metrics in reports understandable by management and business partners
Attention to detail; self-management; problem solving; mentoring
Minimum Education Requirements:
- Bachelor’s degree in engineering, medical, or life sciences preferred.
Other Information:
- Must be able to handle returned complaint samples requiring execution of universal precautions and medical surveillance panel.
This job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. For GMP purposes, the job description should be updated for significant changes. As always, you should consult with your supervisor regarding your actual job responsibilities and any related duties that may be required for the position.
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 an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, 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 help our company develop talented individuals for future leadership roles. Our current groups include: Africa, Middle East, Central Asia Network, African American Network, Chinese Culture Network, Early Career Professionals, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinos at Lilly, PRIDE (LGBTQ + Allies), Veterans Leadership Network, Women’s Network, Working and Living with Disabilities. Learn more about all of our groups.
Full-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 medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
#WeAreLilly