Scientist 1

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 Scientist I supporting cross functional teams, who are responsible for performing a wide variety of functions related to experimental design and analysis of testing utilizing appropriate statistical methodologies. Knowledge of material identification (antibodies and antigens) and protein characterization methods is highly desirable. Typical laboratory instrumentations include but are not limited to: Octet (Biolayer Interferometry), Biacore (Surface Plasmon Resonance), differential scanning fluorimetry (nanoDSF), HPLC, FTIR, SDS-PAGE and IEF gels. Understanding of other characterization tools, such as flow cytometry, and Isothermal Titration Calorimetry is a plus. Strong analytical skills in biophysical characterization and for understanding of protein–protein interactions are preferred. This position is onsite full-time in Rochester, NY. The Responsibilities Performs testing within established timelines to support raw material identification, characterization, and assay concepting of new in vitro diagnostic products and processes. Documents results clearly and accurately. Interprets data and draws conclusions. Readily discriminates between normal and abnormal variation. Presents data to functional project team. Maintains accurate records of work performed in accordance with Current Good Manufacture Process (cGMP) practices, established quality protocols and other standard operating procedures (SOPs). Maintains analytical laboratory equipment related to testing, and performs necessary calibration, QC and documentation per SOPs. Participates in meetings and discussions, helps with ongoing investigations. Communicates with outside vendors and internal business partners Maintains a safe working environment through the proactive identification of hazards and risks. Works cooperatively with others to help a team or work group achieve its goals. Manages inventory. May provide training/ mentorship of new employees on covered jobs and answering job-related questions in one or more areas. Perform other work- related duties as assigned. The Individual Required: BS degree in Biology, Biochemistry, Chemistry, Biotechnology, Analytical Chemistry, Medical Technology or related sciences field; equivalent combination of education and experience. Minimum of 1 year of relevant laboratory experience or an equivalent combination of education and experience. Proficiency in Biomaterial characterization using SDS-PAGE, IEF, Western blotting. Familiarity with analytical techniques such as HPLC and label free binding (Octet and Biacore). Basic knowledge and experience in buffer formulation. Proficiency with Microsoft Office Suite of products. Excellent written and verbal communication skills. Knowledge and experience with Good Documentation Practices (GDP). Knowledge and experience with Good Manufacturing Practices (GMP). Basic understanding of laboratory skills, techniques and data analysis. Ability to carry out general biochemical laboratory procedures including handling of human blood/serum samples,and reagents for testing purposes. Knowledge of safe chemical and biological handling. Less than 10% domestic and/or international travel may be required. This position is not currently eligible for visa sponsorship. Preferred: Experience with cell/tissue cultures Use of Microsoft Access Experience with FT-IR, ELISA plate reader, ITC, flow cytometry Management of cell banks The Key Working Relationships Internal Partners: Works within the R&D project team and has daily interaction for planning and execution of team activities. Cross functional collaboration with many departments and project team members. Meets with cross-functional team members to meet goals External Partners: May interact with outside vendors for arrangement of service or calibration of test equipment or procurement of raw materials or test specimens. How We Work At QuidelOrtho, our culture is shaped by four core behaviors that guide how we collaborate, make decisions, and support each other and those we serve. The ideal candidate will exhibit these behaviors, as we believe they’re essential to how we thrive as a team and achieve meaningful impact: Thrive Together – Collaborate intentionally, grow as a team Make It Happen – Focus on priorities, embrace continuous improvement Commit to Service – Cultivate a service mindset Embrace Inclusion – Be open and authentic, welcome diverse perspectives The 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 at desk, standing or sitting extended periods of time. Flexible work hours to meet project deadlines Working Conditions Noise level: Laboratory sounds or a pitch that may cause distraction. Temperature: May have to perform testing in an environmental chamber (extreme heat, cold, and/or humidity) or work in walk-in refrigerators or freezers. Working around moving machinery Protective equipment required: gloves, lab coat, eyewear Exposures: Biological/biohazardous materials (including but not limited to human or animal blood and blood products, human urine, human CSF), chemical fumes, toxic chemicals, airborne particles, odors, or other unpleasant surroundings Other factors: Possible overtime Physical Demands Computer work, repetitive movements of hand(s), sitting, standing, walking, carrying, reaching. Other physical demands include: Bending Crawling Stooping Vision Climbing or balancing Kneeling Crouching Talking or hearing Tasting or smelling Close Visual Acuity (visual Inspection for small defects or parts, extensive reading or analyzing data.) Intermediate Visual Acuity (operating machines, computer terminal or work at or within arm’s reach). Salary Transparency The salary range for this position takes into account a wide range of factors including education, experience, knowledge, skills, geography, and abilities of the candidate, in addition to internal equity and alignment with market data. At QuidelOrtho, it is not typical for an individual to be hired at or near the top range for their role and compensation decisions are dependent on the facts and circumstances of each case. The salary range for this position is $28/hour to $32/hour and is bonus eligible. 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. Equal Opportunity 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 the 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 [email protected]. #LI-TO1 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. 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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 [email protected] US QuidelOrtho EEO and AAP Policy Statement US Equal Employment Opportunity Posters