Manufacturing Technician II

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.

As we continue to grow as QuidelOrtho, we are seeking an Manufacturing Technician II. Under general supervisor, the scope of this position is responsible for a variety of moderately complex assembly and non-assembly functions in support of manufacturing goals.

This position will be located onsite in San Diego, CA

• Responsible for completing set-up operations for one or multiple of the following: assembly, packaging and prep operations in compliance with approved documentation and QSR

• Responsible for the completion and accuracy of moderately complex documentation associated with the manufacturing processes

• Responsible for cleaning, performing and documenting routine equipment maintenance and minor repair

• Assists in Lean Initiatives, e.g. Kaizen team, metric tracking

• Responsible for record keeping

• Responsible for supporting new equipment installation and validation

• Carries out duties in compliance with established business policies.

• May be required to successfully complete cross-training in other areas

• May be required to assist in training of temporary and manufacturing personnel

• May be required to conduct area clearance signoffs

• May be required to comprehensively review documents and sign for review check

• Perform other duties & projects as assigned.

Required Skills:

• High school diploma or equivalent.

• Two to four years of related experience.

• Knowledgeable of federal and other regulations, e.g. QSR's, ISO, ISO 13485, CMDR

• Computer operated experience required

• Knowledge of MS Office and manufacturing systems required

• Experience with working with semi-automated equipment required

• Basic knowledge of GMP, Documentation Practices required

• Demonstrates commitment to the development, implementation and effectiveness of Quidel Quality Management System per ISO, FDA and other regulatory agencies

• Understands and is aware of the quality consequences which may occur from the improper performance of their specific job. Has awareness of device defects that may occur in their area of responsibility, including product design, verification and validation, manufacturing and testing activities.

Internal: Peers, mechanics, engineers and management

External: Vendors and contractors

The work environment characteristics are representative of a 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 to50 lbs. on a regular basis.May be required to perform repetitive manufacturing processes (e.g., manual lamination, manual cassette assembly, pouch inspection, etc.) up to 90% of workday.Walking, standing, and/orsitting for long periods of time (up to 75% of the day) 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. Personal protective equipment is required as posted.

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

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 $35,700.00 - 66,000.00. 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.

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

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