Automation Engineer (Pharma Manufacturing)

Summary

Responsible for the operation, maintenance, troubleshooting, and continuous improvement of the DeltaV (DCS) to ensure system reliability, availability, and GMP compliance. You will support system lifecycle activities, including change control, deviation investigation, CAPA, qualification/validation, and GMP release to ensure regulatory compliance and data integrity.

Key responsibilities

• Operate, maintain, troubleshoot, and continuously improve the DeltaV (DCS) to ensure system reliability, availability, and GMP compliance
• Operate and maintain DS automation equipment, including UF/DF systems, bioreactors, SoloVPE, LabX, and other process control and analytical systems
• Administer DS computerized systems, including user account management, periodic access review, data backup and recovery, and system time synchronization
• Support system lifecycle activities, including change control, deviation investigation, CAPA, qualification/validation, and GMP release
• Provide technical support for manufacturing operations and troubleshoot automation issues
• Coordinate with vendors and cross-functional teams
• Drive continuous improvement initiatives to enhance system performance and reliability

Requirements:

• Bachelors Degree in biomedical/ pharmaceutical or any relevant courses.
• Min 3 years of relevant experience in a pharmaceutical/biomedical industry
• Familiar with Emerson DeltaV System preferred.
• Familiar with network, domain and other related service preferred.
• Familiar with Data Integrity, 21 CFR Part 11 requirements preferred.
• Familiar with DS process and equipment preferred.