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Cencora is seeking a QA Production team member to oversee daily QA and production activities in a packaging environment. The role involves auditing batch records, performing serialization tasks, and ensuring deviations are documented and investigated.
Strong attention to detail and good communication are essential. The position requires a high school diploma, English literacy, and the ability to work in a team with cross-functional partners across Sampling, Label/Documentation, Production, and
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.
Shift: Sunday-Thursday 11:00pm-7:30am
Pay: $21HR not including shift differential
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.
Requires completion of a high school diploma, general education or GED
The work environment characteristics described here are representative of those a Team Member encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions: The noise level in the warehouse is generally noisy.
The physical demands described here are representative of those that must be met by Team Member to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions: Physical activity requiring reaching, bending, kneeling, stooping, lifting, finger dexterity, grasping, feeling, repetitive motions, talking and hearing. Ability to lift up to 50 lbs. with assistance. Visual requirement is for close vision, distance vision, peripheral vision and ability to adjust focus. Team Member is frequently required to stand, walk (or otherwise be mobile). Ability to deal with stressful situations as they arise.