Robotics and Automation Engineer

2 weeks ago

Carpinteria, California, United States Agilent Full time
Job Overview

Be a part of the evolution in Precision Medicine. Our objective is to enhance the human experience by leveraging the capabilities of precision medicine across laboratories, partners, and patients worldwide.

Within the Diagnostics and Genomics Group (DGG), our Manufacturing Engineering division collaborates closely with various functions in the Order Fulfillment and Supply Chain (OFS) to facilitate the production of highly regulated medical devices essential for physicians in selecting therapies for their patients.

Become an integral member of a dedicated engineering team that plays a crucial role in supporting Finished Production. Our team members are deeply committed to their work as it directly impacts patients battling cancer.

Reporting to the Engineering Manager, you will be a vital part of a cross-functional team of engineers and technicians that is expanding in size and responsibilities as business demands grow.

In this prominent and diverse role, you will deliver hands-on support for production equipment, troubleshooting, repairing, and maintaining critical robotics and automation machinery. You will oversee capital equipment and enhancement projects while collaborating closely with vendors and contractors. Additionally, you will work alongside Quality Assurance in preparing and approving validation and other technical documents and procedures necessary for regulatory compliance.

Key Responsibilities
  • Provide hands-on engineering assistance, troubleshooting, and maintenance of robotic and automated HMLV production floor equipment in a regulated setting.
  • Define, procure, and support robotic and automated filling, labeling, and packaging equipment (SOW, Functional Spec., FAT, SAT).
  • Utilize project management skills and tools to lead and support capital equipment and improvement initiatives.
  • Diagnose equipment failures with a focus on root causes. Lead and assist in defining and implementing corrective and preventive actions (CAPA) and resolutions to audit findings (NCR, SCAR, etc.).
  • Prepare, complete, and support validations (IQ/OQ/PQ/SQ) to comply with applicable FDA and regulatory standards.
  • Support continuous improvement efforts to enhance product quality and reduce manufacturing expenses.
Required Qualifications
  • Bachelor's Degree in Mechanical, Electrical, Robotics, Automation, or other relevant Engineering & Technology disciplines with 4+ years of experience, or an equivalent combination of education and experience.
  • Hands-on experience with Automation and Robotics, PLCs, HMIs.
  • Experience in maintaining robotic & automated equipment.
  • Experience with process/equipment validation: documentation writing and execution - IQ, OQ, PQ.
  • Strong technical, project management, and documentation skills.
  • Self-motivated, highly organized, complex problem solver with a technical, detail-oriented mindset and strong analytical and communication skills.
  • Proven ability to operate in a regulated environment.
Preferred Qualifications
  • Familiarity with FDA QSR requirements, ISO 13485, or other recognized international quality system standards.
  • Experience in working with and/or managing suppliers and/or subcontractors.
  • Knowledge of DI water systems, cold room management, and central monitoring systems.
  • Experience with FMEA, DOE, SPC.
  • Proficiency in CAD, SolidWorks, Siemens NX.
  • Experience with SAP, Agile, Electronic Batch Records (EBR) or Manufacturing Execution Systems (MES), and SCADA.
  • Hands-on experience with programming Fanuc and Denso robots, Omron, Allen Bradley PLC, HMIs, Cognex Vision Systems, Zebra, and Sato Labelers.
  • Understanding of Industry 4.0, AI, predictive analytics, Machine Learning, Data Science, and touchless transactions.
Travel Requirements
Occasional

Work Schedule
Full-time

Shift
Day

Job Function
Manufacturing

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