and Companionship Enriching Life. Elanco's promise to employees: Together, we foster an inclusive culture where everyone can make a difference, encouraging ownership, growth and well-being. Making animals' lives better makes life better- join our team today!
Your Role: QC Coordinator Reports directly to the Manager of Quality Control. The position is responsible for oversight of coordination of all samples being submitted to the Quality Control department for testing of raw materials, bulk product, final product, and experimental samples. Direct interaction with other departments to ensure accuracy of labeling, storage and testing requirements. Organization of controlled documentation
and the distribution of such to laboratories for testing and the organization and finalization of testing government agency submission packets for distribution to QA.
Your Responsibilities: Responsible for the distribution of controlled document Quality Control test data collection sheets Oversight of the sample chain of custody 2020 USDA Samples Submission and shipping Assemble the testing summary reports for non-release testing data for distribution to requesting department Quality Control materials ordering and supply Oversight of electronic based system for any of above. Ie. LIMS, SAP or the implementation of such. What You Need to Succeed: (minimum qualification): GED with
at least 3 years of experience in c GMP or c GXP at an operational level supporting manufacturing in a medical or biotech environment.
Prior experience related to quality control testing or systems in a medical environment with a highly analytical proactive mindset on process improvement. What will give you a competitive edge (preferred qualifications): BA or BS degree in a scientific discipline preferred with at least 3 years of experience in c GMP or c GXP at an operational level supporting manufacturing in a medical or biotech environment. Experience in Materials Management for USDA or FDA regulated industries. Experience in Quality Control testing and environments.
Experience with LIMS, SAP, JMP, Veeva Vault. Excellent technical writing skills. Working knowledge of VICH, USDA and/or EU GMP regulations for veterinary biologics. Additional Information: This is considered a full-time, on-site position. Day shift position. Weekend and evening work not usual, although may be required to provide process support to ongoing operations. Minimal travel requirements
