Scientist III, Quality Control

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 THRIVE as QuidelOrtho, we are seeking a Scientist III, Quality Control. The Scientist III, Quality Control, will be responsible for leading testing stability and final product release activities of Immunohematology reagents. This person will assure compliance with company standards and applicable regulatory agencies. He/She will lead failure investigations to help determine root cause, track and trend data, identify and suggest process improvements to improve business measures.

This is an onsite position in Pompano Beach, Florida.

The Responsibilities

• Organizes and performs product release, stability and raw material testing. Performs testing within established timelines and in accordance with current specifications.

• Documents results clearly and accurately. Interprets results by complying to appropriate specification requirements. Perform data trending of critical product, process information and release test results to be used in SPC/ trend analysis.

• Maintains sufficient inventories off reagents and supplies

• Assures compliance to company procedures, GMP, FDA, Safety and ISO regulations in all functions.

• Participate in laboratory investigations, technology transfer, validation and R&D projects

• Perform other work-related duties as assigned.

The Individual

Required:

• Bachelor of Science degree in Microbiology, Medical Technology, Biology, Chemistry or related field of study and minimum 5-yrs experience

• Manual dexterity to handle instruments, repetitive motions and standing for long periods of time.

• Excellent oral and written communication skills.

• Basic knowledge of Microsoft Office suite of products (Excel, Word, Outlook)

• Ability to prioritize and handle multiple tasks and challenges at the same time

• Work independently and within a team environment

Preferred:

• Knowledge of Immunohematology theory and practice

• Familiarity with FDA, OSHA, ISO, cGMP

The Key Working Interactions

Internal: Manufacturing, Formulations, Quality Control, Quality Assurance, Quality Engineering Product Support.

External: Instrument/Laboratory equipment support personnel – Communicate equipment needs e.g. service and calibration

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. Weekends and overtime may be required.

The Physical Demands

Position requires ability to lift up to 35 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, its 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. A salary range for this position is $80,000 - $100,000. 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

#LI-SP1

---