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Cencora

Distributes medicines and supports patient care

Associate Quality Assurance Quality Operations

Validation, Compliance & Quality SystemsConfirmed live in the last 24 hours
Full-timeColumbus, OH, USA

About the Job

Requirements

  • Completion of a high school diploma, general education, or GED is required.
  • Ability to read and understand English documents, product labels, and instructions, and write accurately when completing production compliance documentation.
  • In-depth knowledge of the function and basic problem-solving capabilities to troubleshoot production issues.
  • Basic mathematical skills are required.
  • Ability to develop and maintain cooperative working relationships.
  • Strong organizational skills and attention to detail.
  • Ability to use good judgment to carry out detailed instructions.
  • Ability to work independently and handle multiple tasks simultaneously.
  • Good verbal and written communication skills.
  • Computer literacy with ERP systems, Microsoft Office (Outlook, Word, and Excel), and computer-based training.
  • Ability to lift up to 50 pounds with assistance and perform physical activities including reaching, bending, kneeling, stooping, lifting, finger dexterity, grasping, feeling, and repetitive motions.
  • Close, distance, and peripheral vision, and the ability to adjust focus.
  • Ability to frequently stand, walk, or otherwise remain mobile, and to deal with stressful situations as they arise.

Responsibilities

  • Provide direction and guidance to daily quality assurance and production activities.
  • Audit production batch records throughout the packaging process for accuracy and compliance, including conducting the final audit before submission to Product Release.
  • Perform serialization activities, including sending print, releasing, suspending, and cloning work orders to support production needs.
  • Verify and correct non-controlled product and packaging component discrepancies in applicable systems.
  • Ensure applicable deviations and supporting documentation are included in the batch record.
  • Perform quality in-process checks as needed.
  • Perform Specific Gravity testing and total organic carbon (TOC) analysis.
  • Perform Cleaning Validation swabbing at the request of the Stability department.
  • Create, review, and update work instructions and standard operating procedures applicable to daily activities.
  • Escalate non-conformance issues during production, lead root-cause analysis of quality incidents, participate in investigation discussions, and draft Unplanned Deviations for management review.
  • Participate in required technical, compliance, and other training as a member of the quality team.
  • Partner with Sampling, Label and Documentation, Production, and Warehouse teams to resolve issues and improve processes through continuous improvement activities that increase efficiency and team member engagement in production.
  • Participate on the site internal audit team representing QA Production.
  • Adhere to current Good Manufacturing Practices, safety regulations, and standard operating procedures, and perform other duties as assigned.

About the Company

Cencora

Distributes medicines and supports patient care

Cencora buys and distributes medicines for pharmacies, hospitals and physician practices, while helping drug manufacturers bring treatments to patients. Its businesses combine wholesale supply networks with specialty distribution for complex therapies and services that support prescribing and patient access. Customers order medicines through its distribution systems, and its teams manage sourcing, storage and delivery alongside pharmacy operations and manufacturer support. It earns revenue from pharmaceutical sales and fees for logistics and healthcare services. The parent company was formed in 2001 through the merger that created AmerisourceBergen, adopted the Cencora name in 2023, and is headquartered in Conshohocken, Pennsylvania.

Company size
10,001+
Company stage
IPO
Headquarters
Conshohocken, PA
Founded
2001

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