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 IndividualRequired 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 r
- 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 RelationshipsInternal:
- Quality
- Maintenance
- Research and Development
- Facilities
- Planning
- Finance
- Engineering Technicians
External:
- Outside service providers
The Work EnvironmentWork environment is representative of manufacturing, laboratory, and office settings. Some travel is required to other production facilities and vendors.
The Physical DemandsPhysical 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.
Salary TransparencyThe 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 $89,008.92 - $102,000.00 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.
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