Equipment Engineer

Equipment Engineer

QuidelOrtho 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 Role

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.

The Responsibilities

• 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

The Individual

Required Skills

• 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
• This position is not currently eligible for visa sponsorship.

Preferred Skills:

• Experience in electrical-mechanical theory and application, manufacturing and fabrication process, automated assembly, 2D & 3D CAD, programmable logic controls, measurement methods, hardware design, pneumatics, basic finance theory, and basic quality tools preferred.

• The Key Working Relationships

Internal:

• Quality
• Maintenance
• Research and Development
• Facilities
• Planning
• Finance
• Engineering Technicians

External:

• Outside service providers

• The Work Environment

• Work environment is representative of manufacturing, laboratory, and office settings. Some travel is required to other production facilities and vendors.

• The Physical Demands

• Physical demands require the individual to lift loads up to 50lbs, work within restricted areas confined by equipment, and work within a low humidity environment with potential exposure to biological, toxic, and corrosive reagents (50% of time). The individual is also required to work within the confinements of a cubical style office, and also within a laboratory setting (50%). Must be willing to work flexible hours, including after-hour on-call support of manufacturing equipment and lines.

• 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.