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.

As we continue to grow as QuidelOrtho, we are seeking an Operator II, Packaging Manufacturing in the Slide Assembly Department. This position is responsible for quality and maintaining the highest standards in compliance within company policies, procedures and all applicable regulations. Accountable for adhering to all EHS guidelines.

This position is located in Rochester, NY.

Work Schedule: "Firemen's Rotation": Two 12 hour days (6:00am-6:00pm) followed by two 12 hour nights (6:00pm-6:00am)

• Operate manufacturing machinery in PKG Manufacturing.

• Utilize inspection tools, including visual inspection, to assess product quality.

• Adhere to all approved and documented processes.

• Work closely with maintenance/engineering to minimize equipment downtime.

• Work closely with other manufacturing support areas to coordinate activities.

• Maintain a clean & orderly work environment.

• Escalate issues to supervisor, mechanic, or engineer.

• Participate in effective shift crossovers.

• Work closely with peers.

• Accurately complete documentation to ensure acceptable quality records.

• Maintain individual training records.

• Work with computer controlled equipment and processes.

• Follow safety procedures and practices.

• Perform other duties as assigned.

• A minimum of a High School diploma or equivalent required.

• A minimum of 6 months of related experience within a manufacturing environment.

• Experience in a regulated industry (cGMP, SOPs, audits, etc).

• Proficiency in computers (i.e.; email, internet explorer, MS Word, etc).

• Strong communication skills: Reading, writing, and team interaction.

• Dependable team player with a "can-do" attitude.

• Experience with SAP preferred.

• Experience with Lean Manufacturing preferred.

• Exhibit an ability of mechanical aptitudepreferred.

Internal Partners: Maintenance, Engineering, Quality

External Partners: Suppliers

The work environment characteristics are representative of a manufacturing, laboratory, or warehouse environment and include handling of viral and bacterial hazards, potentially hazardous chemicals, as well as infectious or potentially infectious bodily fluids, tissues, and samples. Up to 75% of the time you will be, standing, walking or sitting for extended periods of time. Ability to lift up to 50 lbs. Flexible work hours to meet project deadlines.

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