Job Details

The Opportunity QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine. We are more than 6,000 strong and do business in over 130 countries, providing answers with fast, accurate and consistent testing where and when they are needed most - home to hospital, lab to clinic. Our culture puts our team members first and prioritizes actions that support happiness, inspiration and engagement. We strive to build meaningful connections with each other as we believe that employee happiness and business success are linked. Join us in our mission to transform the power of diagnostics into a healthier future for all. The Role The Packaging Specialist I is responsible for supporting the packaging and assembly of products as required by the production schedule. Included are all production reagents which form the kit components, from the raw materials through to bottled and labeled finished goods. This role is located in Athens, Ohio. The Responsibilities Supports all packaging processes by following the work steps and instructions given by the Packaging Supervisor or equivalent. Satisfies due dates as specified in the Master Production Schedule with high quality product at or below cost targets. Ensures all packaged and labeled components meet visual and integrity specifications by working closely with QC and other production persons. Conducts in-process checks and inspection of packaged product as required. Maintains an orderly and clean working environment. Responds to all audits of production areas in a pro-active, constructive manner by resolving deficiencies and implementing corrective actions. Works on assignments that are routine in nature, however, due to the large number of unique protocols/processes, position requires careful attention to detail and strict adherence to formally approved production documentation. Performs work with near perfect accuracy with no deviations from the accepted practices. Emphasis is placed on the methods to maintain control and achieve reproducibility, which is critical for compliance with Quidel's Quality System regulations. Carries out duties in compliance with established business policies. The Individual Required: High school diploma or equivalent and/or a minimum of 1 year of related experience in a manufacturing environment. Careful attention to detail and strict adherence to formally approved production documentation. Flexibility with the ability to follow directions from a variety of people. Organizational abilities Ability to work as a team player. Preferred: Familiarity with current GMP and ISO quality regulations and comfort working in a highly structured, documented environment. Familiarity with basic laboratory devices and equipment preferred. The Key Working Relationships Internal Partners: Packaging Supervisor, Manufacturing Manager, Packaging Specialists and Quality Control The Work Environment Work environment is a combination of manufacturing and laboratory settings. Long hours are occasionally required in order to comply with the Master Schedule and manufacturing demands. Must have ability to manipulate packaging, ability to hear and operate laboratory machinery, and visually monitor products for Quality Standards. It is essential to maneuver easily throughout the laboratory environment and have the ability to lift a minimum of 30 lbs. Position requires standing and/or sitting for extended periods of time. Essential functions are subject to change as other duties may be assigned. Equal Employment Opportunity QuidelOrtho believes in Equal Opportunity for all and is committed to ensuring all individuals,