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
In accordance with forecasted production requirements and assignment, the Laboratory Technician III assists with manufacturing products within ISO regulations, reviewing/reconciling documents and work orders, supporting assigned projects with supervision, and maintaining daily adherence to Production goals relating work order closure, and schedule adherence.
This role will be located in San Diego.
The Responsibilities
- Manufactures or provides manufacturing support while adhering to regulatory requirements and business polices /procedures and schedules.
- Supports Chemists in departmental troubleshooting and process improvements.
- Carries out laboratory activities in support of production schedules and objectives as directed by senior staff.
- Safely operates laboratory equipment in accordance with established practices.
- Promotes and be responsible for laboratory safety and housekeeping.
- Obtains and stocks laboratory supplies as directed.
- Maintains documentation and records in an accurate, timely and thorough manner.
- Promotes and be responsible for inventory accuracy
- Simultaneously performs multiple tasks as required.
- Participates in Lean Activities.
- Responsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company’s policies and practices.
- Perform other duties & projects as assigned.
The Individual
Required
- AA/AS Degree or higher plus 0-2 years of related experience or High School Diploma plus 2 to 4 years of work experience in a GMP environment. Previous training and experience in the operation of lab equipment and use of lab chemicals and tools preferred.
- Basic mathematical skills
- General computer knowledge
- Good organizational skills
- Laboratory skills, such as reagent/solution preparation, pipetting and testing
- Good verbal and written communication skills
- Good interpersonal skills
- Knowledge cGMPand cGLP
- Ability to follow basic instructions, maintain accurate records and notes, and the ability to carry out assignments in a thorough, conscientious fashion.
- Understands and is aware of the quality consequences which may occur from the improper performance of their specific job.
The Key Working Relationships
Internal Partners
Inventory Control, Quality, Facilities, IT, Safety,
The Work Environment
The work environment characteristics are representative of a laboratory 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 production demand. Position requires ability to lift up to 30 lbs. on a regular basis. Up to 75% of time at lab or production environment 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.
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 $57,000.00 - $98,000.00 USD. 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.