Equipment Engineer

Quidel Ortho develops and manufactures advanced diagnostic solutions that make a meaningful difference in the lives of millions of people every day. United by a shared purpose, our passionate, driven employees come together to transform data into understanding and action for healthcare professionals, patients and communities around the world. Together, we’re creating a lasting impact where it is needed most and advancing the power of diagnostics for a healthier future for all.

The Equipment Engineer provides engineering expertise in the areas of new product development, process development and improvement, equipment and sustaining engineering, manufacturing technologies, and project support to ensure the production of world class products.

This is an onsite role in Carlsbad, CA.

• Selects, manages, integrates, installs, diagnoses, and operates various manufacturing equipment, robotics, programmable logic controls, electropneumatics, measurement tools, and other equipment for manual and automated assembly manufacturing lines.
• Works closely with vendors and can lead moderately sized capital equipment projects. This can include regular design reviews, milestone setting, and travel to vendors.
• Writes, executes, and reviews documentation for production operations including manufacturing and equipment instructions, validation protocols, design control, pFMEA, and control plans for new, modified, and relocated equipment.
• Develops manufacturing control plans and metrics that verify machine outputs are compliant with QSR standards.
• Creates, maintains, and improves manufacturing documentation including SOPs, work instructions, BOMs, and routings.
• Works closely with other staff to deploy and train on new procedures and instructions.
• Analyzes measurement, machine, process, and product data with basic statistical methods.
• Monitors and improves key performance metrics such as yield, scrap, OEE, and throughput.
• Identifies and implements new technologies and continuous improvement to optimize manufacturing process output.
• Works closely with cross‑functional teams involving R&D, Quality, Operations, Supply Chain, and external partners, providing engineering guidance for projects and problem‑solving activities.
• Support or lead audits, CAPA investigations, NCR resolution, and change control (ECOs) activities.
• Organizes and manages team meetings, generates agendas, and writes meeting minutes.
• Develops and maintains budgets for multi‑tasked projects and conducts the financial analysis necessary to justify procurement of new capital equipment and supports the development of contractual agreements that incorporate supplier accountability for cost, schedule, and quality.
• Interprets and generates mechanical part designs via CAD models, piece part drawings, and assembly drawings.
• Fabricates piece parts or modifies equipment as needed, using common fabrication methods such as conventional milling, turning, laser cutting, welding, and soldering.
• Able to complete basic component electrical wirings, including the ability to interpret electrical drawings.
• Perform other work‑related duties as assigned.

• BS degree in an engineering discipline, preferably Mechanical, Manufacturing or Industrial Engineering or equivalent work experience.
• 3 years of experience in a pharmaceutical or medical device environment in a high-volume manufacturing environment.
• Subject matter expert on more than one piece of equipment and/or manufacturing process.
• Understands cGMP and lean manufacturing principles.
• Problem solving skills
• Excellent verbal and written communication skills r
• This position is not currently eligible for visa sponsorship.

• Experience in electrical‑mechanical theory and…