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

At QuidelOrtho, we’re advancing the power of diagnostics for a healthier future for all. Join our mission as our next Production Chemist. Under minimal ongoing supervision, this position is responsible for a variety of manufacturing support functions involving the operation of lab equipment and conduct of procedures/tasks according to established GMP under the direction of senior staff including manufacturing products within QSR and ISO regulations

This position will be onsite in San Diego, CA.

The Responsibilities

Carries out production tasks in support of manufacturing goals and objectives
Participates in Lean Initiatives
Operates laboratory equipment safely, as trained and directed, in accordance with established practices
Maintains records and notebooks as directed in a neat, thorough and accurate manner. Perform required data entry on company planning and materials management system
Ensures materials are appropriately labeled, approved for use and in sufficient quantity to complete required tasks
Reviews/reconciles documents and work orders. Writes/revises documentation as needed
Supports product transfers
May Train other chemists/lab technicians
Partners with the planners, provide input into weekly schedule
Initiates and participates in lead document revisions to ensure accurate BOM's process descriptions, NCMR and deviations
Operates laboratory equipment and perform routine maintenance/repair
Follows all safety guidelines, manufacturing policies and procedures. Operate under strict QSR and ISO compliance
Performs complex formulations, component and material evaluations, equipment calibrations and maintenance
Formulates complex chemistries and solutions as directed, following established guidelines and procedures
Carries out duties in compliance with established business policies
Performs other duties & projects as assigned
Participates in product/process troubleshooting and validations
Carries out functions which may require multiple task coordination
Covers on call assignment and complies with all restrictions and requirements
Assesses issues affecting departmental performance, Quality standards, and product quality Individually communicates to management and initiates appropriate corrective action
Supports departmental troubleshooting, cross-functional projects and process improvement teams
Perform other work-related duties as assigned

The Individual

Required:

High School Diploma plus 5-8 years of related work experience in a GMP environment, or
BA or BS in Chemistry, Biological Sciences, and 2-4 years of related experience in a GMP environment, or
Master’s degree in Chemistry, Biological Sciences, or equivalent and 0-2 years of related experience in GMP environment required
Ability to follow detailed instructions, maintains accurate records and notes, and carries out assignments in a thorough, conscientious fashion while adhering to safe laboratory practices
Knowledge of a variety of lab equipment and their operation
Ability to carry out experiments following established guidelines and summarize results accurately
Strong problem-solving and troubleshooting skills
Strong verbal and written communication skills
Organized and detail oriented
Ability to work in a team environment
General computer knowledge
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
This position is not currently eligible for visa sponsorship.

Preferred:

Previous training and experience in the operation of lab equipment and use of lab chemicals and tools preferred.

The Key Working Relationships

Internal Partners:

Manufacturing, Materials, Technical Support and Quality Assurance

The 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.

The Physical Demands

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 $67,303.53 - $75,000.00 and is bonus eligible. 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 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 the 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.

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