Position Overview
The Lead Automation Engineer will be responsible for overseeing the design, implementation, and maintenance of DeltaV automation systems within pharmaceutical manufacturing facilities projects. This role requires a deep understanding of automation technologies and their application in the pharmaceutical industry, ensuring compliance with regulatory standards while optimizing production processes.
Key Responsibilities
- Automation System Management:Design, develop, and implement DeltaV automation systems to enhance manufacturing efficiency and quality.
Oversee the maintenance and troubleshooting of DeltaV systems, ensuring minimal downtime and maximal reliability.
- Project Leadership:Lead automation projects from conception through implementation, including budgeting, scheduling, and resource allocation.
Coordinate with cross-functional teams including process engineers, quality assurance, and IT to ensure seamless integration of DeltaV solutions.
- Regulatory Compliance:Ensure all automation systems comply with relevant regulatory standards (e.g., FDA, EMA, HSA) and Good Manufacturing Practices (GMP).
Prepare and maintain documentation for validation and compliance audits.
- Technical Expertise:Stay updated with the latest advancements in DeltaV and other automation technologies and their applications in the pharmaceutical industry.
Provide technical guidance and training to the engineering team and production staff.
- Continuous Improvement:Identify opportunities for process improvements through automation and implement changes to enhance productivity and quality.
Analyze system performance and make data-driven recommendations for optimization.
Qualifications
- Education:Bachelor's or Master's degree in Automation Engineering, Electrical Engineering, Computer Science, or a related field.
- Experience:Minimum of 6 years of experience in automation engineering, with at least 3 years in a leadership role within the pharmaceutical industry.
Proven experience in designing and managing DeltaV automation systems in a GMP-regulated environment.
