Senior Operator
About The Position
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 As we continue to grow as QuidelOrtho, we are seeking a Fluids Manufacturing Operator III to work in our Rochester, NY fluids manufacturing location. The Operator III performs operations as described by SOPs under Good Manufacturing Practices (GMPs). The ideal candidate would be an experienced operator who is able to lead and coach others. The candidate will exhibit accountability by being able to adjust to changing business needs and identify and support implementation opportunities for improving workflow and resources within the Work Center. They will be responsible to follow the production schedule and prioritize the workload. This position is in Rochester, NY. Work Schedule: B-Shift (3:00pm -11:00pm)
Requirements
- HS Diploma or Equivalent required.
- Minimum of 4-6 Years industry experience.
- Effective communicator who is open to training other operators on procedures.
- Demonstrate a strong understanding of the process in order to properly perform the assigned manufacturing tasks.
Nice To Haves
- Strong working knowledge and understanding of packaging and filling equipment.
- Experience with Microsoft office/SAP system.
Responsibilities
- Execute manufacturing or manufacturing-support processes according to standard operating procedures.
- Maintain working knowledge of cGMP requirements to ensure adherence to compliance policies and regulations.
- Sets up and operates production equipment to produce work in process and finished goods.
- Take samples for further downstream testing according to standard procedures.
- Use of ERP system for performing material transactions.
- Cleans, maintains, and performs basic repairs on equipment as needed.
- Operate and troubleshoot equipment in clean room and non-clean room environment.
- Accurately complete documentation in batch records, logbooks, forms and other GMP documents as required.
- Wear the appropriate PPE when working in manufacturing and other working environments.
- Demonstrate training progression, train designated personnel in all levels of responsibility
- Perform other duties as assigned.
Benefits
- QuidelOrtho offers a comprehensive benefits package including medical, dental, vision, life, and disability insurance, along with a 401(k) plan, employee assistance program, Employee Stock Purchase Plan, paid time off (including sick time), and paid Holidays.
- All benefits are non-contractual, and QuidelOrtho may amend, terminate, or enhance the benefits provided, as it deems appropriate.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED
Number of Employees
1,001-5,000 employees
