Operator, Film Slitting

QuidelOrtho•Rochester, NY

1d•Onsite

About The Position

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 our Slitting Department to perform operations as described by our Standard Operating Procedures (SOPs) under Good Manufacturing Practices (GMPs) in our Film manufacturing Department. The Slitter performs slitting, packaging, storage, and tracking of clinical chemistry webs in accordance with product and machine standards, while using computer systems to monitor quality and inventory and supporting troubleshooting efforts as needed. This position is in Rochester, NY.

Requirements

Required High School Diploma or GED.
3 years work experience and a minimum of 3 months experience in operations/manufacturing environment (prefer a regulated industry).
Strong mechanical aptitude with the ability to troubleshoot processes and equipment.
Proficient in reading and writing English.
Basic proficiency in Microsoft Office (Word, Excel, Outlook).

Nice To Haves

2–3 years of experience in chemical/solution prep, recipe-driven processes, solvent/aqueous coating, or mechanical assembly.
Vocational or technical education.
Knowledge of GMP or ISO regulations.

Responsibilities

Review all procedures, instruction sheets, and temporary orders prior to each slitting event to ensure accuracy.
Operate slitting machines in strict accordance with standard operating procedures (SOPs), ensuring equipment and work areas are clean and production-ready.
Monitor production parameters and specifications in real-time to ensure product quality and consistency.
Maintain precise records in both hard copy and electronic formats, utilizing SAP and ET systems for documentation and label verification.
Adhere to GMP and safety protocols, reporting any deviations and assisting with the maintenance and updating of slitting procedures.
Manage material inventory, including retrieving supplies from the dock and ensuring the proper sealing, conditioning, and storage of finished product.
Collect and process samples according to product standards, overseeing packaging, shipping, and delivery requirements.
Support engineering and process teams in troubleshooting equipment issues and resolving production challenges.
Condition and maintain interleaving paper and other required consumables in accordance with specifications.
Uphold high housekeeping standards throughout all phases of the slitting process to ensure a safe and efficient work environment.
Perform other work-related duties as assigned.