Quality Assurance Coordinator

Neogen Corporation•Lexington, KY

10d•Onsite

About The Position

Come Be Part of a Mission that Matters! This role involves a variety of quality assurance tasks within manufacturing operations, focusing on auditing, tracking quality metrics, assisting with audits, maintaining documentation, inspecting materials, and managing records related to deviations and investigations. The position also includes sampling and testing of raw materials and finished goods, assisting with stability programs, and participating in physical inventories.

Requirements

High school diploma
Two years related experience
A clear understanding of quality assurance
Ability to read, analyze and interpret common regulatory documents
Ability to respond to common inquiries or complaints from customers, regulatory agencies or members of the business community
Ability to effectively present information to management and public groups
Ability to work with mathematical concepts such as probability and statistical inference and fundamentals of scientific analysis such as mean, median, mode, coefficient of variation and standard deviation
Direct experience with Windows-based computers, use of personal computer, keyboard and software packages including; Windows, Microsoft Office, and Solomon
Ability to define problems, collect data, establish facts, and draw valid conclusions
Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with abstract and concrete variables
Must have a valid driver’s license

Responsibilities

Auditing batch records and manufacturing procedures
Tracking of quality metrics associated with manufacturing operations or other areas as deemed necessary by the organization
Assisting in ISO audits
Assisting or conducting internal audits, as necessary
Assisting with/writing of standard operating procedures (SOP) and forms related to the Animal Safety Manufacturing Operations
Maintaining control of the Master Document List including all Master Batch Records and SOPs
Assisting with/issue all documents, SOPs, and forms as needed
Maintaining all records associated with operations including, but not limited to, completed batch records, on-site training records, completed validations, equipment calibration records, completed equipment qualification records
Inspecting and releasing of all raw materials, including labels, inserts, components, containers and closures
Inspecting and releasing of finished goods or disposition of non-conforming material
Maintaining the records associated with deviations or non-conformances and the associated investigations, actions, and follow ups
Sampling raw materials and initiate testing with laboratories
Assisting with the sampling of finished goods and delivery to the appropriate laboratory (ies) for testing
Assisting in maintaining stability programs
Assisting in physical inventories