Perform routine operational support and Investigative tasks involved in the investigation of suspect samples (e.g., sample log-in, photographs, packaging variable data verification, packaging evaluations, physical appearance, etc.).(NOTE: This position will only perform first person analysis)Perform non-routine sample analyses of suspect samples utilizing screening technologies.Produce quality documentation for internal and external use and ensure data documentation meets ALCOA plus expectations.Learn and utilize basic development, manufacturing, and regulatory processes, and develop an awareness of analytical and pharmaceutical industry trends related to product authentication.Work collaboratively with people in AQCO and with cross-functional business partners.Work safely and in compliance with applicable quality, environmental, and safety expectations. Ensure compliance with applicable Lilly global standards and regulatory guidelines.As needed within the AQCO organization, this position will help with shipping and purchasing needs
