Scientist I

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 Scientist 1. The Scientist I in the Analytical Laboratory assures the suitability of raw materials and in process solutions by executing complex analytical testing. This testing uses a variety of instrumentation including, but not limited to, pH meter, UV-VIS spectrophotometers, automated enyzmatic systems, particle sizers, GC, viscometers, FTIR, Titrimeters, ovens and lyophilization. All testing with the previous mentioned instruments require precision and accuracy from this position. The Scientist I will maintain instrumentation, calibrations and maintenance logs. Also, runs quality controls and analyzes required testing as needed. In addition, the Scientist 1 works under the guidance of senior laboratory staff and management to resolve routine to complex analytical quality issues, assist in laboratory investigations / validation projects. Position requires enzyme kit and control making and leading a crossover in the lab. Completion of Non-Conformance Records and/or Quality Investigations in a timely manner is required for this position. Work is scheduled, supervised, and follows established methods and procedures (SOPs).

This position is located in Rochester, NY.

The Responsibilities

• Completes raw material and in process tests supporting DFM by executing analytical testing on multiple types of equipment in compliance with all procedures; and provides analytical and manual dexterity to deliver accurate and precise results from complex analytical methods analyzes data for accuracy, trends, precision, investigation reports per documented specifications.
• Maintains enzyme kits and controls. This includes quarterly counts, making new batches when current batch is low, leading a crossover effort in the lab, and writing a report.
• Participates in/or assists in laboratory investigations, instrument and/or method validations/verifications. Also, participates in raw material validations for product support and completes non-conformance records in a timely manner.
• Maintains equipment, chemical inventory, and prepares reagents and buffers.
• Performs necessary housekeeping to ensure the laboratory is continuously maintained in safe, orderly and compliant condition.
• Works in PPE.
• Must adhere to quality, GLP, GMP and regulatory compliance policies.
• Schedule Info: 40+ Hours/ wk on a rotational shift schedule Monday - Friday
  (Occasional Saturday may be required based on business need and lab staffing)
• Works weekly rotational shift schedule as assigned, schedules are subject to change per business requirements. Current rotational schedule is A shifts (7:00 am -3:10 pm), B shifts (3:00pm - 11:10PM) and C shifts (11 pm - 7:10 am). The standard 5 week scheduled rotation for a laboratory member is AACCB, but is subject to change depending on business or laboratory needs.
• Perform other work-related duties as assigned.

The Individual

Required:

• Minimum BS degree in scientific or related field; equivalent combination of education and experience may be considered.
• Strong mathematical skills.
• Strong problem-solving skills and attention to detail.
• Ability to work independently and as part of a team. Candidate must have a demonstrated proven track record of planning and organization of daily workload, high affinity toward teamwork and demonstrated problem solving using innovative solutions.
• Having a working knowledge of computers and windows software is desired. Full understanding of quality control is expected.
• This position requires an individual who can multi-task, adapt to changes in daily workload and priorities, and function in a cross-functional team setting.

Preferred:

• 0 to 2 years of work experience in Chemistry, Biology, Microbiology, Quality, Regulatory, or Compliance in a highly regulated manufacturing environment (Diagnostics, Medical Device, Pharmaceutical or Consumer).

The Key Working Relationships

Internal: Management, Production Engineers, Maintenance Operators, Quality Analysts/Scientists, and Quality Engineers

External: Outside Vendors and Instrument Service Personnel

The Work Environment

The work environment characteristics are representative of an office, laboratory and manufacturing environment and may include handling of viral and bacterial hazards as well as infectious or potentially infectious bodily fluids, tissues and samples. Flexible work hours to meet project deadlines.

Position requires ability to lift up to 50 lbs., work within restricted areas confined by equipment. Up to 50% of time/work within a low humidity environment and/or extreme cold environment with potential exposure to biological, toxic and corrosive reagents; and up to 50% is required to work within the confinements of a cubical style office, and also within a laboratory setting. Walking, standing and sitting for longs periods of time are routine to accomplish tasks in this role. Specific vision abilities required by this job include close and distance vision and the ability to adjust focus. Position requires use of Personal Protective Equipment as posted.

Essential functions are subject to change as other duties may be assigned.

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 $40,500.00 - 73,800.00. 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.

EEO

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 [email protected]

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