Associate Operator

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

Under close supervision, the Associate Operator is responsible for a variety of assembly and non-assembly functions in support of manufacturing goals.

This role is located in Athens, Ohio.

The Responsibilities 

• Operates equipment used to manufacture products

• Checks and inspects products against departmental procedures

• Responsible for recognizing product or equipment problems that arise during the manufacturing process

• Maybe required to assist with the set-up and clean-up of manufacturing equipment

• Responsible for Lean Initiatives

• Carries out duties in compliance with established business policies

• Performs other duties & projects as assigned

The Individual

Required:

• 0 - 2 years of related experience

• Basic knowledge of regulations (FDA, ISO, OSHA, etc.)

• Demonstrates commitment to the development, implementation and effectiveness of Quidel Quality Management System per ISO, FDA and other regulatory agencies

• Understands and is aware of the quality consequences which may occur from the improper performance of their specific job. Has awareness of device defects that may occur in their area of responsibility, including product design, verification and validation, manufacturing and testing activities

Preferred:

• High school diploma or equivalent

• Experience in medical device manufacturing

• MS Office and manufacturing systems

The Key Working Relationships

Internal Partners:

Mechanics, Engineers and Management Team

The Work Environment

The work environment characteristics are representative of a manufacturing environment and may include handling of viral and bacterial hazards as well as infectious or potentially infectious bodily fluids, tissues and samples. Flexible work hours to meet project deadlines. Works on assignments that are routine in nature.

The Physical Demands

The work environment characteristics are representative of a manufacturing environment and may include handling of viral and bacterial hazards as well as infectious or potentially infectious bodily fluids, tissues and samples. Flexible work hours to meet project deadlines. Works on assignments that are routine in nature.

Equal Employment Opportunity

QuidelOrtho believes in Equal Opportunity for all and is committed to ensuring all individuals, including individuals with disabilities, have an opportunity to apply for those positions that they are interested in and qualify for without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, age, veteran status, disability, genetic information, or any other protected characteristic. QuidelOrtho is also committed to providing reasonable accommodations to qualified individuals so that an individual can perform their duties. If you are interested in applying for an employment opportunity and require special assistance or an accommodation to apply due to a disability, please contact us at [email protected].

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