Scientist II (Donor Screening)
This job is no longer available
There are still lots of open positions. Let's find the one that's right for you.
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. As we continue to grow, we're seeking a Scientist II to join our Donor Screening operations. This position is primarily responsible for testing microplates that are coated with Antigens, formulation and in-process testing of reagents, conjugates and controls for Donor Screening Kit Components according to established procedures or approved protocols. Need to be familiar with multiple testing / formulation labs in Donor Screening Area. Donor Screening Kit for ELISA Test System includes the following seven components that are product-specific: positive control, negative control, conjugate-antibody, antigen-coated microwell plates, specimen diluent, substrate buffer and o-phenylenediamine 2-HCl tablets. This results in common manufacturing sub-process steps that include formulation of multiple bulks and antigen-coated microplate process. It includes receipt and inspection of incoming raw materials, microplate coating and testing, formulation and in-process testing of reagents, conjugates and controls, filtration and filling of bulks, and release testing followed by kit packaging. Manufactured finished goods are released on acceptable in-process, QA release testing along with concurrent CBER lot release according to set specifications. This position is located onsite in Raritan, NJ.
