Quality Operations Associate

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply todayJob DetailsShift Hours:Sunday- Thursday 3:00PM- 11:30PMPlease note, flexibility in schedule will be required based on business needs, this can include working different hours or days.This position is located onsite at our facility in Columbus, OH. There is no option for remote or hybrid work.This role is in support of American Health Packaging, a Cencora business offering pharma packaging services in the US.The Quality Operations Associate provides guidance and direction to daily Quality and Production activities tomaintaincompliance with corporate and regulatory requirements.Provides direction and guidance to daily QA and Production activities. Could include but not limited to the following activities:Audits production batch records throughout the packaging process for accuracy and compliance. Conducts final audit prior to submitting to Product Release.Performs serialization activities, including but not limited to sending print, releasing, suspending, and cloning a work order to support production needs.Verifies and corrects non-controlled product and packaging component discrepancies within the applicable systems.Ensures applicable deviations and supporting documentation is provided in the batch record.Performs Quality in-process checks as needed.Performs Specific Gravity testing and TOC analysis.Performs Cleaning Validation swabbing upon the request of the Stability department.Creates, Reviews and Updates WIs and SOPs applicable to daily activities.Escalates non-conformance issues during the production process to management and leads the root cause analysis of quality incidents, participates in investigation discussions, and drafts Unplanned Deviations prior to submitting it for management review.Actively engages in all technical training, as well as compliance and other training required as a member of the quality team. Works in partnership with supporting areas (Sampling, Label and Documentation, Production, Warehouse) to resolve issues and improve processes by participating in continuous improvement activities to increase efficiency and Team Member engagement in the production area.Participates on the site internal audit team representing QA Production.Adheres to all cGMP, safety regulations, and understands SOP's.Performs all other duties as assigned.Education & Experience:Requires completion of a high school diploma, general education degree (GED) or equivalent combination of experience and education.Requires five or more (5+) years of equivalent work experience.Familiar with quality assurance concepts,practicesand procedures in packaging of pharmaceuticals.Skills & Knowledge:Ability to read and understand the English language for the purpose of reading documents, productlabelsand instructions.Must have good written skills for the purpose of accurately completing compliance documentation for production -depth knowledge of the function and basic problem-solving capabilities for the purpose of troubleshooting issues during production activities.Mustpossessbasic mathematical skills.Strong interpersonalskills;ability to develop andmaintaincooperative working relationships with others.Strong organizational skills as well as detail oriented.Ability to use good judgementin order tocarry out detailed instructions.Ability to work independently and handle a variety of tasks simulta

Created: 2026-01-19