Packaging Specialist

7 days ago


OH United States Quidel Corporation Full time
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 a team of over 6,000 strong, operating in over 130 countries, providing fast, accurate and consistent testing where and when it's needed most - from home to hospital, lab to clinic.

Our culture prioritizes employee happiness, inspiration and engagement, recognizing that employee well-being and business success are linked.

The Role

The Packaging Specialist I is responsible for supporting the packaging and assembly of products as required by the production schedule.

This includes all production reagents which form the kit components, from raw materials through to bottled and labeled finished goods.

This role is located in Athens, Ohio.

Responsibilities
  1. Support all packaging processes by following work steps and instructions given by the Packaging Supervisor or equivalent.
  2. Satisfy due dates as specified in the Master Production Schedule with high quality product at or below cost targets.
  3. Ensure all packaged and labeled components meet visual and integrity specifications by working closely with QC and other production persons.
  4. Conduct in-process checks and inspection of packaged product as required.
  5. Maintain an orderly and clean working environment.
  6. Respond to all audits of production areas in a pro-active, constructive manner by resolving deficiencies and implementing corrective actions.
Requirements

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.



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