Tech Ops Process Engineer

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 6000 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 were advancing the power of diagnostics for a healthier future for all. Join our mission as our next Technical Operations Process Engineer. This position independently supports manufacturing operations by applying engineering and scientific principles to improve process performance resolve issues and ensure product quality. This role leads routine technical activities and contributes to process development validation and continuous improvement initiatives.

This position will be onsite in San Diego CA.

The Responsibilities

• Independently execute process optimization characterization and validation activities

• Lead portions of technical transfer projects from R&D to Manufacturing

• Own investigations for NCs CAPAs and deviations of moderate complexity

• Design and analyze DOE studies; implement data-driven improvements

• Develop process and material specifications

• Author and revise technical documentation (SOPs validation protocols/reports)

• Execute change plans from feasibility assessment through implementation ensuring alignment with cross-functional stakeholders and business objectives

• Support supplier qualification activities and material characterization efforts

• Contribute to continuous improvement initiatives

• Ensure compliance with QMS and regulatory requirements

• Perform other work-related duties as assigned

The Individual

Required:

• Bachelors degree (BS/BA) in Engineering or related technical field

• 35 years of experience in a cGMP-regulated manufacturing environment or equivalent

• Strong analytical thinking and structured problem-solving capabilities

• Experience with process development optimization scale-up and standardization

• Proficiency in Design of Experiments (DOE) Statistical Process Control (SPC) and data analysis

• Ability to independently design experiments interpret data and make data-driven decisions

• Experience with process validation (IQ/OQ/PQ) and technical documentation

• Knowledge of quality systems cGMP regulations and compliance requirements

• Strong project management skills with ability to manage multiple priorities and meet deadlines

• Effective written and verbal communication skills

• Ability to work both independently and collaboratively across cross-functional teams

• Proficiency with standard computer applications (e.g. Microsoft Office data analysis tools)

• Ability to troubleshoot and resolve complex technical issues with minimal supervision

• Strong organizational skills and attention to detail

• Demonstrated ability to drive continuous improvement initiatives

• Capable of working in a fast-paced regulated manufacturing environment

• This position is not currently eligible for visa sponsorship.

Preferred:

• Six Sigma certification (Green Belt or Black Belt)

The Key Working Relationships

Internal Partners:

Quality Control Quality Assurance Manufacturing R&D Chemistry Regulatory Engineering and Supply Chain

External Partners:

Suppliers and Customers

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

The Physical Demands

Sitting standing walking lifting carrying reaching pushing and pulling. Other physical demands include bending crawling stooping vision grasping climbing or balancing kneeling crouching talking or hearing. Position may be required to use 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 $89008.92 - $105000 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 .

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