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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 Quality Control Technician I. This position is primarily responsible for performing Quality Control testing products at various stages of Production. This includes both routine (SOP) and special assignments, as well as documentation of findings/results for attachment to Device History Records. Additionally, this individual will lend support as necessary to the daily QC Chemistry core functions - Stability Studies, Raw Material Testing, Proficiency Testing, and Customer Complaints. This will be an on site position in San Diego.
The Responsibilities
Performs and documents QC Testing of WIP Production Lots and special evaluation assignments
Supports daily QC Chemistry core functions as needed
Performs and documents final QC Testing
Supports new product development/improvement projects
Performs general housekeeping and laboratory organization
Carries out duties in compliance with established business policies
Works and communicates effectively and professionally with others
Operates laboratory equipment safely, as trained and directed, in accordance with established practices
Perform other work-related duties as assigned
The Individual
High School diploma or equivalent required
0-2 years' in Quality Control or manufacturing laboratory environment
Ability to read, interpret and follow detailed procedures, instructions and drawings
Solid understanding of QSRs/ISO
General chemistry and laboratory skills, GLP/GMP experience
Demonstrated team-oriented interaction skills/professional behavior
Strong written and verbal communication skills
Computer skills, including word processing, spreadsheet creation and manipulation, report generation, email, etc. required
Must know basic quality terms, definitions and concepts
Must understand traceability (product, material, and calibration)
Possesses the ability to discern product and process integrity to defined standards and methods, with the initiative to take appropriate action
Preferred, but not required:
Experience working with a microscope preferred
Work Environment
The work environment characteristics are representative of an office, laboratory, and manufacturing environment and include handling of viral and bacterial hazards, potentially hazardous chemicals, 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 20 lbs. on a regular basis. Up to 90% of time at lab bench or desk, walking, standing, and sitting for long 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. Must have the ability to operate lab equipment. Position requires use of Personal Protective Equipment as posted.
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
"At Ortho Clinical Diagnostics, we are proud of the empowering, inclusive and innovative culture we are growing. Our team is passionate about our work, and brings deep knowledge, industry experience and diverse thinking that drive results, making Ortho a place to grow your career.
Ortho Clinical Diagnostics is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other characteristic protected by law."