Operator, Slides Manufacturing
QuidelOrthoAbout the role
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
At QuidelOrtho, we’re advancing the power of diagnostics for a healthier future for all. Join our mission as our next Operator 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)
The Responsibilities
Operate manufacturing machinery in Slide 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 work-related duties as assigned.
The Individual
Required:
A minimum of a High School diploma, GED.
A minimum of 6 months of related experience within a manufacturing environment.
Ability to perform basic machine adjustments
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.
Preferred:
Experience with SAP.
Experience with Lean Manufacturing.
Exhibit an ability of mechanical aptitude.
Key Working Relationships
Internal Partners: Maintenance, Engineering, Quality
External Partners: Suppliers
Work Environment
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
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