Operator III, Formulations

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

We're seeking a Formulation Operator III who will be responsible for preparing buffers and solutions, performing antibody dilutions, treating gels, calibrating instruments, and cleaning and processing equipment used in manufacturing and formulation. Additional responsibilities include supporting other departmental activities in accordance with established procedures.

This position is located in Pompano Beach, Florida.

Work Schedule : Monday-Friday A shift 8 : 00am to 4 : 30pm, occasional Saturdays as needed based on production needs.

The Responsibilities

Perform automated and manual cleaning of manufacturing and formulation equipment.

Perform assembly, inspection, and issue of manufacturing equipment.

Perform formulation of buffers and solutions.

Perform dilutions of Monoclonal and Polyclonal Antibodies.

Perform gel treatment processes such as the addition of Sodium Azide to Gel and Antibody to Gel.

Perform daily / weekly / monthly verification and maintenance of the DI Water System and daily / weekly maintenance of the automated washer.

Perform calibration and testing of formulation department instruments used for chemistry testing. Perform Formulation department instrument calibrations / maintenance. Support Projects.

QC incoming receipt and inspection of raw materials.

Perform other work-related duties as assigned.

The Individual

Required :

An Associate of Science degree in Biology, Chemistry, or a related field, or a minimum of three years of experience in compounding and formulations. A combination of education and experience will also be considered.

Preferred :

A minimum of one year in a regulated production environment with knowledge of Good Manufacturing Practices. Familiarity with FDA, OSHA, ISO and cGMP.

Experience working with chemical / biological formulations.

Be and advocate for a safe work environment and be responsible for personal safety and the safety of others.

Manual dexterity for the processing and cleaning of manufacturing and formulation equipment, repetitive motions and standing for extended periods of time.

Excellent oral and written communication skills.

Ability to prioritize and manage multiple tasks and challenges at the same time.

Work independently and within a team environment.

Key Working Relationships

Internal Partners : Manufacturing, Quality Control, Microbiology, Quality Assurance, Engineering, Product Support, Materials Management.

External Partners : None

Work Environment

A GMP licensed biologics manufacturing facility. Works primarily in the Formulation Department and in the Clean Room located within the Manufacturing Department. Weekends and Overtime may be required.

Physical Demands

Frequent standing and sitting and repetitive hand movements. Close visual acuity required.

Room temperature laboratory with refrigerators of 2C to 8C.

Protective equipment such as gloves, safety glasses, lab coat and vinyl aprons required as needed.

Exposure to steam and chemicals.

Exposure to hazardous chemicals.

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 hourly range for this position is $23.38 to $27.00 hourly. 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 .