Why This Role Stands Out
This hybrid role at Abbott Laboratories offers a fantastic opportunity to lead impactful automation projects within the thriving medical technology sector, fostering significant career growth and skill development in a highly reputable company. You'll thrive here if you are a mid-senior engineer passionate about innovation, continuous improvement, and mentoring others in a collaborative environment. Apply now to contribute to life-changing diagnostics and medical products!
Quick Overview
Job Description
Abbott Laboratories is seeking a Staff Equipment and Automation Engineer to lead design, implementation, and optimization of automated production systems for diagnostics and medical products. In this role, you will own full lifecycle equipment projects-from requirements and concept development through installation, validation, and continuous improvement-ensuring reliability, compliance, and throughput in a regulated (FDA/ISO) environment. You will collaborate with manufacturing, quality, and R&D to introduce new technologies, drive root cause analysis, reduce downtime, and standardize best practices across sites while mentoring junior engineers.
Responsibilities
- Lead design, commissioning, and optimization of automated manufacturing and test equipment
- Plan and execute equipment validation (IQ/OQ/PQ) and documentation in compliance with FDA/ISO and c
- GMPDrive continuous improvement to increase throughput, OEE, and equipment reliability
- Implement automation solutions including PLCs, robotics, vision systems, and data acquisition
- Lead root cause investigations and corrective actions for equipment and process issues
- Collaborate with Manufacturing, Quality, and R&D on new product introductions and tech transfers
- Manage capital equipment projects including scope, schedule, budget, and vendor coordination
- Develop and maintain technical documentation, SOPs, and maintenance standards
- Ensure equipment safety, regulatory compliance, and audit readiness
- Mentor junior engineers and technicians, sharing best practices and technical expertise
Required Skills
- Equipment validation (IQ/OQ/PQ)
- Automation system design (PLC/SCADA/HMI)c
- GMP and FDA/ISO regulatory compliance
- Process optimization and OEE improvement
- Root cause analysis and corrective actions
- Project management for capital equipment
- Technical documentation and protocols
- Data acquisition and manufacturing analytics
- Robot/automated material handling systems
- Cross-functional collaboration with QA/RA/Operations
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