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 Specialty Fluids Formulation Scientist II. Performing various assignments related to the formulation of control, reference fluids, linearity, math model, interferent fluids, and other miscellaneous fluids for internal use in final support of the VITROS analyzer systems. These fluids are produced in the manufacturing facilities in Rochester, NY in accordance with cGMP regulations. This position is located in Rochester, NY.

The Responsibilities

Perform various assignments related to the formulation of control, reference fluids, linearity, math model, interferent fluids, and other miscellaneous fluids.

Preparation of complex biological solutions using established protocols. 

Weighing of chemicals, volumetric additions of various biological components, filtration, ultra-filtration, filling, intermixing, aseptic handling, etc. 

Interpret laboratory data to make appropriate adjustments to formulations and performs calculations for chemical additions and corrective actions to the various specialty formulations. 

Providing technical support to the formulation group in the operations area and maintaining control substance inventory following DEA regulations and audit preparedness.

Performs other work-related duties as assigned.

The Individual

Required:

Bachelor’s Degree in biology, chemistry or equivalent field.

Minimum of 2-5 years of experience in a related field.

Working knowledge of chemical and/or biological processes.

Strong attention to detail and problem-solving ability; including identifying potential root causes and recommending potential corrective actions is required.

Must be comfortable working in a manufacturing environment that requires resolution of urgent product release issues in a timely manner and flexibility to adjust to changing priorities.

Strong verbal and written communication skills required.

Preferred:

Experience with Quality System SOPs and laboratory GMP is desired.

Understanding of the interrelationship of these disciplines as applied to medical devices in clinical chemistry would be desired. 

Experience with VITROS MicroSlide and/or MicroTip products and with VITROS analyzers is highly desired.

Experience with Process Excellence tools or methodologies, Quality programs (Trackwise and Windchill) is not a requirement but would be an asset. 

Proficiency in computer programs such as Excel, Word and SAP is strongly recommended.

The Work Environment

The work environment characteristics are representative of a laboratory and manufacturing environment and include handling of potentially hazardous chemicals, as well as infectious or potentially infectious bodily fluids and/or samples.  Manual dexterity to handle instruments, complete repetitive motions, and stand for long periods of time is required.  Diligent use of PPEs (Personal Protective Equipment) to limit exposure to bloodborne pathogens is required.  Up to 75% of time spent in the lab, standing for extended periods of time.  Flexible work hours to meet manufacturing deadlines.

Salary Transparency

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 that facts and circumstances of each case. Salary range for this position is $74,000 to $129,000 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 Employment 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 their 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.

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