Scientist I (Assay Development)

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

QuidelOrtho is seeking a Scientist I to support R&D at our Canal Ponds, Rochester, NY location. The Scientist I will work in a team environment on all phases in support of Assay Development. The Scientist will perform various assignments related to the experimental design and testing of assay performance on the VITROS and other QuidelOrtho products in the laboratory in accordance with cGMP regulations. Preferred candidate has a minimum of 6 months experience running VITROS analyzers. This position will also include documentation and summarization of the experimental data. Additional laboratory work may include preparation of complex biological solutions using established protocols, including reconstitution of calibrators and controls. These protocols may include weighing chemicals, volumetric additions of various biological components, pipetting, filtration, ultra-filtration, etc.

This position is onsite full-time in Rochester, NY.

The Responsibilities

• As part of a technical team; create, execute, and understand experimental test designs for the VITROS analyzers to complete testing aimed for the verification and validation of new vitro diagnostic products or processes using established protocols and SOP's.
• Provide technical support by executing test designs on diagnostic instruments to drive accurate test results.
• Maintain analyzer equipment related to the VITROS testing (daily, weekly, and monthly maintenance) and perform necessary calibration, QC, and documentation according to SOPs.
• Maintain accurate records of work performed in accordance with cGMP and the procedures outlined in the Quality System. This includes Design History files, QC, equipment maintenance, and other associated testing documentation.
• Maintain a neat, orderly, and safe workplace and clean work area and analyzer upon test completion.
• Perform training on SOP's, protocols, and other laboratory documents
• Perform other work-related duties as assigned.

The Individual

Required:

• BS in Clinical Laboratory Science / Medical Technology, Chemistry, Biology or related field or equivalent combination of education and experience.
• Minimum of 1 year experience in a lab environment is required. Basic understanding of laboratory skills and techniques (weighing, pipette use, volumetric measure, etc.) are required.
• Familiarity with safe chemical and biological handling required.
• Basic computer skills (MS Word, MS Excel) are required.
• Pay attention to detail
• Work collaboratively or alone
• Excellent verbal and written communication skills will be required.
• Travel 5% - Infrequent
• This position is not currently eligible for visa sponsorship.

Preferred:

• Ability to do some level of troubleshooting
• Ability to present information cross functionally

The Key Working Relationships

Internal Partners:

• Internal partners: RND, Quality, Regulatory, PMO, Marketing

External Partners:

• External partners: Customer sites, vendor interaction

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

Physical Demands

• Standing - Frequent
• Bending - occasional
• Stooping - occasional
• Lifting - < 10 lbs occasionally
• Vision - spend time on computer and equipment GUI
  

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 $30.00/hour to $32.00/hour. 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 recruiting@quidelortho.com.